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Treatment of Skin Disease E-Book

Treatment of Skin Disease E-Book

Mark G. Lebwohl | Warren R. Heymann | John Berth-Jones | Ian Coulson

(2013)

Additional Information

Book Details

Abstract

Treatment of Skin Disease is your definitive source for managing the complete range of dermatologic conditions you’re likely to encounter in practice. This medical reference book boasts an intuitive and easy to use format that covers the full spectrum of options, equipping you with not only standard treatment strategies, but second- and third-line therapies for instances when other alternatives fail. You’ll be thoroughly prepared to offer your patients the expertly informed medical care they deserve when facing common or complex dermatologic diseases.

  • Consult this title on your favorite e-reader, conduct rapid searches, and adjust font sizes for optimal readability.
  • Address your most difficult clinical challenges by having every possible therapy option at your disposal, including third- and fourth-line therapies, as well as standard treatments for dermatologic disorders.
  • Apply the in-depth knowledge of leading dermatologists through a summary of each treatment strategy along with detailed discussions of treatment choices.
  • Gain insight to the essential features which define each dermatologic disease with chapters presented in a tabular format, using checklists of diagnostic and investigative pearls and color-coded boxed text, for quick at-a-glance summaries of key details.
  • Make the most informed decisions possible with the inclusion of up-to-date evidence levels throughout the text.
  • Stay abreast of emerging drug treatments and research with the very latest options for the 251 most common dermatologic conditions, and take advantage of today’s expert knowledge on hot topics in dermatology such as bed bugs, erosive pustular dermatosis, polycystic ovary syndrome, and more.
  • Achieve effective visual diagnoses by viewing over 250 full-color clinical images of skin diseases, most of which are brand new in this edition.

Table of Contents

Section Title Page Action Price
Front cover cover
Treatment of Skin Disease i
Copyright page iv
Table of Contents v
Preface xi
List of Contributors xiii
Acknowledgements xxv
Dedication xxv
Evidence Levels xxvi
A: Double-Blind Study xxvi
B: Clinical Trial ≥20 Subjects xxvi
C: Clinical Trial <20 Subjects xxvi
D: Series ≥5 Subjects xxvi
E: Anecdotal Case Reports xxvi
1 Acanthosis nigricans 1
Management strategy 1
Specific investigations 1
Prevalence and significance of acanthosis nigricans in an adult population. 1
Prevalence of obesity, acanthosis nigricans and hyperinsulinemia in an adolescent clinic. 1
Juvenile acanthosis nigricans. 1
Acanthosis nigricans associated with insulin resistance: pathophysiology and management. 1
Genes, growth factors and acanthosis nigricans. 2
Characterization of groups of hyperandrogenic women with acanthosis nigricans, impaired glucose tolerance and/or hyperinsulinemia. 2
Malignant acanthosis nigricans: a review. 2
Acanthosis nigricans: a new manifestation of insulin resistance in patients receiving treatment with protease inhibitors. 2
Acanthosis nigricans-like lesions from nicotinic acid. 2
Somatotrophin-induced acanthosis nigricans. 2
First-line therapy 2
Acanthosis nigricans: a cutaneous marker of tissue resistant to insulin. 2
Clearance of acanthosis nigricans associated with the HAIR-AN syndrome after partial pancreatectomy: an 11-year follow up. 2
Acanthosis nigricans in association with congenital adrenal hyperplasia: resolution after treatment. 2
Second-line therapy 2
Topical therapy with tretinoin and ammonium lactate for acanthosis nigricans associated with obesity. 2
Acanthosis nigricans and hypovitaminosis A. Response to topical vitamin A acid. 2
Successful symptomatic tazarotene treatment of juvenile acanthosis nigricans of the familial obesity-associated type in insulin resistance. 2
Treatment of mixed-type acanthosis nigricans with topical calcipotriol. 2
Therapeutic approach in insulin resistance with acanthosis nigricans. 2
Using trichloroacetic acid in the treatment of acanthosis nigricans: a pilot study. 2
Third-line therapy 3
Treatment of acanthosis nigricans with oral isotretinoin. 3
Improvement of acanthosis nigricans on isotretinoin and metformin. 3
Effect of ketoconazole in the hyperandrogenism, insulin resistance and acanthosis nigricans (HAIR-AN) syndrome. 3
Malignant acanthosis nigricans: potential role of chemotherapy. 3
Treatment of acanthosis nigricans with cyproheptadine. 3
Acanthosis nigricans. 3
Remission of acanthosis nigricans associated with polycystic ovarian disease and stromal luteoma. 3
Treatment of acanthosis nigricans of the axillae using a long-pulsed (5-msec) alexandrite laser. 3
Continuous-wave carbon dioxide laser therapy of pseudoacanthosis nigricans. 3
2 Acne keloidalis nuchae 4
Management strategy 4
Specific investigations 4
First-line therapies 5
Pseudofolliculitis barbae. 5
An open label study of clobetasol propionate 0.05% and betamethasone valerate 0.12% foams in the treatment of mild to moderate acne keloidalis. 5
Acne keloidalis is a form of scarring alopecia. 5
Second-line therapies 5
Folliculitis nuchae scleroticans – successful treatment with 13-cis-retinoic acid (isotretinoin). 5
Third-line therapies 5
The surgical management of extensive cases of acne keloidalis nuchae. 5
Surgical excision of acne keloidalis nuchae with secondary intention healing. 5
3 Acne vulgaris 6
Management strategy 6
Specific investigations 7
First-line therapy 7
European evidence-based (S3) guidelines for the treatment of acne. 7
Topical retinoids in acne – an evidence-based overview. 7
Clinical evidence for the role of a topical anti-inflammatory agent in comedonal acne: findings from a randomized study of dapsone gel 5% in combination with tazarotene cream 0.1% in patients with acne vulgaris. 7
Effects of benzoyl peroxide 5% clindamycin combination gel versus adapalene 0.1% on quality of life in patients with mild to moderate acne vulgaris: a randomized single-blind study. 7
A randomized, single-blind comparison of topical clindamycin + benzoyl peroxide and adapalene in the treatment of mild to moderate facial acne vulgaris. 7
A randomized, single-blind comparison of topical clindamycin + benzoyl peroxide (Duac) and erythromycin + zinc acetate (Zineryt) in the treatment of mild to moderate facial acne vulgaris. 8
Study of the efficacy, tolerability, and safety of 2 fixed-dose combination gels in the management of acne vulgaris. 8
Clindamycin phosphate/tretinoin gel formulation in the treatment of acne vulgaris. 8
What’s new in antibiotics in the management of acne? 8
Isotretinoin: state of the art treatment for acne vulgaris. 8
Hormonal antiandrogens in acne treatment. 8
Efficacy and safety of 3 mg drospirenone/20 mcg ethinylestradiol oral contraceptive administered in 24/4 regimen in the treatment of acne vulgaris: a randomized, double-blind, placebo-controlled trial. 8
Efficacy of a combined oral contraceptive containing 0.030 mg ethinylestradiol/2 mg dienogest for the treatment of papulopustular acne in comparison with placebo and 0.035 mg ethinylestradiol/2 mg cyproterone acetate. 8
Second-line therapy 8
Efficacy of topical azelaic acid gel in the treatment of mild-moderate acne vulgaris. 9
Combination of azelaic acid 5% and clindamycin 2% for the treatment of acne vulgaris. 9
Dapsone gel 5% for the treatment of acne vulgaris: safety and efficacy of long-term (1 year) treatment. 9
Dapsone gel 5% in combination with adapalene gel 0.1%, benzoyl peroxide gel 4% or moisturizer for the treatment of acne vulgaris: a 12-week, randomized, double-blind study. 9
A pilot study of the safety and efficacy of picolinic acid gel in the treatment of acne vulgaris. 9
New and emerging treatments in dermatology: acne. 9
Randomized trial comparing a chemical peel containing a lipophilic hydroxy acid derivative of salicylic acid with a salicylic acid peel in subjects with comedonal acne. 9
Combination of azelaic acid 5% and erythromycin 2% in the treatment of acne vulgaris. 9
Lack of irritative potential of nadifloxacin 1% when combined with other topical anti-acne agents. 9
Zileuton, a new efficient and safe systemic anti-acne drug. 9
Application of the essential oil from copaiba (Copaifera langsdori Desf.) for acne vulgaris: a double-blind, placebo-controlled clinical trial. 9
The efficacy of 5% topical tea tree oil gel in mild to moderate acne vulgaris: a randomized, double-blind placebo-controlled study. 9
A 10% glycolic acid containing oil-in-water emulsion improves mild acne: a randomized double-blind placebo-controlled trial. 10
Lasers and photodynamic therapy for the treatment of acne. 10
Photodynamic therapy with intralesional 5-aminolevulinic acid and intense pulsed light versus intense pulsed light alone in the treatment of acne vulgaris: a comparative study. 10
Long-pulsed dye laser versus long-pulsed dye laser-assisted photodynamic therapy for acne vulgaris: a randomized controlled trial. 10
An assessment of the efficacy of blue light phototherapy in the treatment of acne vulgaris. 10
Clinical efficacy of home-use blue-light therapy for mild-to moderate acne. 10
Comparison of red and infrared low-level laser therapy in the treatment of acne vulgaris. 10
Clinical evaluation of a 1450-nm diode laser as adjunctive treatment for refractory facial acne vulgaris. 10
Cyproterone acetate loading to lipid nanoparticles for topical acne treatment: particle characterisation and skin uptake. 10
The efficacy of topical cyproterone acetate alcohol lotion versus placebo in the treatment of the mild to moderate acne vulgaris: a double blind study. 10
A review of phytotherapy of acne vulgaris: perspective of new pharmacological treatments. 10
Current state of acne treatment: highlighting lasers, photodynamic therapy, and chemical peels. 10
Superficial chemical peels and microdermabrasion for acne vulgaris. 10
Third-line therapy 10
Evidence and considerations in the application of chemical peels in skin disorders and aesthetic resurfacing. 11
Management of acne scarring, Part I: a comparative review of laser surgical approaches. 11
Deep peeling using phenol versus percutaneous collagen induction combined with trichloroacetic acid 20% in atrophic post-acne scars; a randomized controlled trial. 11
Treatment of acne scars by fractional bipolar radiofrequency energy. 11
Acne scars in ethnic skin treated with both non-ablative fractional 1,550 nm and ablative fractional CO2 lasers: comparative retrospective analysis with recommended guidelines. 11
Treatment of facial scarring: lasers, filler, and nonoperative techniques. 11
4 Acrodermatitis enteropathica 12
Management strategy 12
Specific investigations 12
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal regions 8q24.3. 12
Identification of SLC39A4, a gene involved in acrodermatitis enteropathica. 12
Bullous lesions in acrodermatitis enteropathica delaying diagnosis of zinc deficiency: a report of two cases and review of the literature. 12
First-line therapy 12
Zinc deficiency in acrodermatitis enteropathica: multiple dietary intolerance treated with synthetic diet. 13
Acrodermatitis enteropathica and other zinc deficiency disorders. 13
Acrodermatitis enteropathica and an overview of zinc metabolism. 13
Acknowledgment 13
5 Actinic keratoses 14
Management strategy 14
Specific investigations 14
Actinic keratoses and the incidence of occult squamous cell carcinoma: a clinical–histopathologic correlation. 14
Clinical recognition of actinic keratoses in a high-risk population: how good are we? 14
First-line therapies 15
A randomized controlled trial to assess sunscreen application and beta carotene supplementation in the prevention of solar keratoses. 15
Reduction of solar keratoses by regular sunscreen use. 15
A prospective study of the use of cryosurgery for the treatment of actinic keratoses. 15
Effect of a 1 week treatment with 0.5% topical fluorouracil on occurrence of actinic keratosis after cryosurgery. 15
Imiquimod 5% cream for the treatment of actinic keratosis: results from two phase III, randomized, double- blind, parallel group, vehicle-controlled trials. 15
Imiquimod 2.5% and 3.75% for the treatment of actinic keratoses: results of two placebo-controlled studies of daily application to the face and balding scalp for two 3-week cycles. 15
Imiquimod 2.5% and 3.75% for the treatment of actinic keratoses: results of two placebo-controlled studies of daily application to the face and balding scalp for two 2-week cycles. 15
A randomised study of topical 5% imiquimod vs. topical 5-fluorouracil vs. cryosurgery in immunocompetent patients with actinic keratoses: a comparison of clinical and histological outcomes including 1-year follow-up. 15
Guidelines on the use of photodynamic therapy for nonmelanoma skin cancer: an international consensus. 15
Intraindividual, right–left comparison of topical methyl aminolaevulinate–photodynamic therapy and cryotherapy in subjects with actinic keratoses: a multicentre, randomized controlled study. 15
Multicentre intraindividual randomized trial of topical methyl aminolaevulinate–photodynamic therapy vs. cryotherapy for multiple actinic keratoses on the extremities. 16
Photodynamic therapy with aminolevulinic acid topical solution and visible blue light in the treatment of multiple actinic keratoses of the face and scalp: investigator-blinded, phase 3, multicenter trials. 16
Results of an investigator-initiated single-blind split-face comparison of photodynamic therapy and 5% imiquimod cream for the treatment of actinic keratoses. 16
Second-line therapies 16
Assessment of adapalene gel for the treatment of actinic keratoses and lentigines: a randomized trial. 16
Three percent diclofenac in 2.5% hyaluronan gel in the treatment of actinic keratoses: a meta-analysis of the recent studies. 16
Diclofenac sodium 3% gel for the management of actinic keratosis: 10+ years of cumulative evidence of efficacy and safety. 16
Ingenol mebutate gel for actinic keratosis. 16
Randomized, double-blind, double-dummy, vehicle-controlled study of ingenol mebutate gel 0.025% and 0.05% for actinic keratosis. 16
Third-line therapies 16
Full face laser resurfacing: therapy and prophylaxis for actinic keratoses and non-melanoma skin cancer. 17
Recurrence rates and long-term follow-up after laser resurfacing as a treatment for widespread actinic keratoses on the face and scalp. 17
Nonablative fractional photothermolysis for facial actinic keratoses: 6-month follow-up with histologic evaluation. 17
A clinical comparison and long-term follow-up of topical 5-fluorouracil versus laser resurfacing in the treatment of widespread actinic keratoses. 17
Long-term efficacy and safety of Jessner’s solution and 35% trichloroacetic acid vs 5% fluorouracil in the treatment of widespread facial actinic keratoses. 17
Dermabrasion for prophylaxis and treatment of actinic keratoses. 17
6 Actinic prurigo 18
Management strategy 18
Specific investigations 18
Actinic prurigo – a specific photodermatosis? 18
Actinic prurigo among the Chimila Indians in Colombia: HLA studies. 18
Actinic prurigo: an update. 18
HLA-DR4 may determine expression of actinic prurigo in British patients. 18
Actinic prurigo and HLA-DR4. 18
Association of HLA subtype DRB10407 in Colombian patients with actinic prurigo. 18
Actinic prurigo: clinical features and HLA associations in a Canadian Inuit population. 18
Actinic prurigo of the lower lip – review of the literature and report of five cases. 19
Follicular cheilitis – a distinctive histopathologic finding in actinic prurigo. 19
Actinic prurigo cheilitis: clinicopathologic analysis and therapeutic results in 116 cases. 19
Augmentation of ultraviolet erythema by indomethacin in actinic prurigo: evidence of mechanism of photosensitivity. 19
First-line therapies 19
Topical photoprotection for hereditary polymorphic light eruption of American Indians. 19
Actinic prurigo deterioration due to degradation of DermaGard window film. 19
Treatment of actinic prurigo with intermittent short-course topical 0.05% clobetasol 17-propionate: a preliminary report. 19
Narrow-band UVB (TL-01) phototherapy: an effective preventative treatment for the photodermatoses. 19
The quality of life of 790 patients with photodermatoses. 19
Second-line therapies 19
Controlled trial of methoxsalen in solar dermatitis of Chippewa Indians. 19
Treatment of actinic prurigo with PUVA: mechanism of action. 19
Thalidomide in the treatment of actinic prurigo. 19
Thalidomide in actinic prurigo. 19
Third-line therapies 20
Hereditary polymorphic light eruption in American Indians: photoprotection and prevention of streptococcal pyoderma and glomerulonephritis. 20
Pentoxifylline in the treatment of actinic prurigo: a preliminary report of 10 patients. 20
Treatment of actinic prurigo in Chimila Indians. 20
The clinical features and management of actinic prurigo: a retrospective study. 20
Actinic prurigo: clinico-pathological correlation. 20
Use of topical cyclosporine for conjunctival manifestations of actinic prurigo. 20
Topical cyclosporine in the treatment of ocular actinic prurigo. 20
7 Actinomycosis 21
Management strategy 21
Clinical review: Actinomycosis. 21
Susceptibility of pathogenic actinomycetes to antimicrobial compounds. 21
Specific investigations 21
Diagnostic methods for human actinomycosis. 21
Cervicofacial actinomycosis: diagnosis and management. 21
Diagnosis of pelvic actinomycosis by 16S ribosomal RNA gene sequencing and its clinical significance. 21
Cervicofacial actinomycosis: CT and MR imaging findings in seven patients. 21
First-line therapies 21
Antimicrobial susceptibility testing of Actinomyces species with 12 antimicrobial agents. 22
Actinomycosis. 22
Actinomycosis and nocardiosis. A review of basic differences in therapy. 22
Second-line therapies 22
The use of oral amoxycillin for the treatment of actinomycosis: a clinical and in vitro study. 22
Actinomycosis abscess of the thyroid gland. 22
Successful treatment of thoracic actinomycosis with ceftriaxone. 22
Mandibular actinomycosis treated with oral clindamycin. 22
Clindamycin in the treatment of cervicofacial actinomycosis. 22
Clindamycin in the treatment of serious anaerobic infections. 22
Primary actinomycosis of the hand: a case report and literature review. 22
Actinomycosis of the prostate. 22
Actinomycosis of the temporomandibular joint. 22
Use of imipenem in the treatment of thoracic actinomycosis. 22
Report of eight cases of pulmonary actinomycosis and their treatment with imipenem–cilastatin. 22
Cutaneous disseminated actinomycosis in a patient with acute lymphocytic leukemia. 22
Antibiotic treatment of cervicofacial actinomycosis for patients allergic to penicillin: a clinical and in vitro study. 22
Primary actinomycosis of the quadriceps. 22
Comparative in vitro susceptibilities of 396 unusual anaerobic strains to tigecycline and eight other antimicrobial agents. 22
Third-line therapies 23
Treatment of recalcitrant actinomycosis with ciprofloxacin. 23
Treatment of pulmonary actinomycosis with levofloxacin. 23
Treatment of pulmonary actinomycosis with rifampin. 23
Pulmonary actinomycosis. Rapid improvement with isoniazid and rifampin. 23
Adjunctive hyperbaric oxygen therapy for actinomycotic lacrimal canaliculitis. 23
Hyperbaric oxygen in the treatment of actinomycosis. 23
8 Acute generalized exanthematous pustulosis 24
Management strategy 24
Specific investigations 24
First-line therapies 24
Risk factors for acute generalized exanthematous pustulosis (AGEP) – results of a multinational case-control study (EuroSCAR). 24
Acute generalized exanthematous pustulosis. Analysis of 63 cases. 24
Acute generalized exanthematous pustulosis (AGEP) – a clinical reaction pattern. 25
Acute generalized exanthematous pustulosis. 25
Pustular eruption after drug exposure: is it pustular psoriasis or a pustular drug eruption? 25
Generalized pustular psoriasis or drug-induced toxic pustuloderma? The use of patch testing. 25
A systemic reaction to patch testing for the evaluation of acute generalized exanthematous pustulosis. 25
Second-line therapies 25
Acute generalised exanthematous pustulosis. 25
9 Allergic contact dermatitis and photoallergy 26
Management strategy 26
Specific investigations 27
Contact dermatitis: allergic. 27
First-line therapies 27
A double-blind randomized placebo-controlled pilot study comparing topical immunomodulating agents and corticosteroids for treatment of experimentally induced nickel contact dermatitis. 27
Efficacy of topical corticosteroids in nickel-induced contact allergy. 27
The effect of two moisturisers on skin barrier damage in allergic contact dermatitis. 27
Tacrolimus 0.1% vs mometasone furoate topical treatment in allergic contact hand eczema: a prospective randomized clinical study. 27
SDZ ASM 981 is the first non-steroid that suppresses established nickel contact dermatitis elicited by allergen challenge. 27
Efficacy and safety of oral alitretinoin (9-cis retinoic acid) in patients with severe chronic hand eczema refractory to topical corticosteroids: results of a randomized, double-blind, placebo-controlled, multicentre trial. 27
Efficacy and tolerability of alitretinoin for chronic hand eczema under daily practice conditions: results of the TOCCATA open study comprising 680 patients. 27
Treatment with topical tacrolimus favors chronic actinic dermatitis: a clinical and immunopathological study. 27
Second-line therapies 27
Chronic eczematous dermatitis of the hands: a comparison of PUVA and UVB treatment. 28
Azathioprine versus betamethasone for the treatment of Parthenium dermatitis: a randomized controlled study. 28
Oral cyclosporine inhibits the expression of contact hypersensitivity in man. 28
Treatment of parthenium dermatitis with methotrexate. 28
A double-blind study of Grenz ray therapy in chronic eczema of the hands. 28
Disulfiram and low nickel diet in the management of hand eczema: a clinical study. 28
Azathioprine treatment in chronic actinic dermatitis: a double-blind controlled trial with monitoring of exposure to ultraviolet radiation. 28
Chronic actinic dermatitis: an analysis of 51 patients evaluated in the United States and Japan. 28
Actinic reticuloid: response to cyclosporine. 28
Psoralen plus UVA protocol for Compositae photosensitivity. 28
Chronic actinic dermatitis treated with mycophenolate mofetil. 28
Third-line therapies 28
The effect of the topical application of different pentoxifylline concentrations on the patch test results of nickel-sensitive patients. 28
10 Alopecia areata 29
Management strategy 29
Specific investigations 30
First-Line therapies 30
A comparison of intralesional triamcinolone hexacetonide and triamcinolone acetonide in alopecia areata. 30
Intralesional treatment of alopecia areata with triamcinolone acetonide by jet injector. 30
Diphencyprone in the treatment of alopecia areata. 30
Topical immunotherapy with diphenylcyclopropenone in the treatment of chronic extensive alopecia areata. 30
Fexofenadine hydrochloride enhances the efficacy of contact immunotherapy for extensive alopecia areata: retrospective analysis of 121 cases. 30
Second-Line therapies 30
Clobetasol propionate 0.05% under occlusion in the treatment of alopecia totalis/universalis. 30
Efficacy and safety of a new clobetasol propionate 0.05% foam in alopecia areata: a randomised, double-blind, placebo-controlled trial. 30
Treatment of alopecia areata by anthralin-induced dermatitis. 30
Topical tretinoin as an adjunctive therapy with intralesional triamcinolone acetonide for alopecia areata. Clinical experience in northern Saudi Arabia. 30
Comparative assessment of topical steroids, topical tretinoin (0.05%) and dithranol paste in alopecia areata. 30
Topical minoxidil solution (1% and 5%) in the treatment of alopecia areata. 31
Bimatoprost in the treatment of eyelash universalis alopecia areata. 31
Latanoprost in the treatment of eyelash alopecia in alopecia areata universalis. 31
Lack of efficacy of topical latanoprost and bimatoprost ophthalmic solutions in promoting eyelash growth in patients with alopecia areata. 31
Treatment of alopecia areata with three different PUVA modalities. 31
Effects of psoralen-UVA-turban in alopecia areata. 31
Third-Line therapies 31
High-dose pulse corticosteroid therapy in the treatment of severe alopecia areata. 31
Placebo-controlled oral pulse prednisolone therapy in alopecia areata. 31
Oral cyclosporine for the treatment of alopecia areata. 31
Evaluation of oral minoxidil in the treatment of alopecia areata. 32
Treatment of persistent alopecia areata with sulfasalazine. 32
Efficacy and tolerability of methotrexate in severe childhood alopecia areata. 32
Could azathioprine be considered as a therapeutic alternative in the treatment of alopecia areata? A pilot study. 32
Inosiplex for treatment of alopecia areata: a randomized placebo-controlled study. 32
A parallel study of inosine pranobex, diphencyprone and both treatments combined in the treatment of alopecia totalis. 32
Treatment of alopecia areata with topical nitrogen mustard. 32
Topical nitrogen mustard in the treatment of alopecia areata: a bilateral comparison study. 32
Dermatography as a new treatment for alopecia areata of the eyebrows. 32
Effect of superficial hypothermic cryotherapy with liquid nitrogen on alopecia areata. 32
Use of the pulsed infrared diode laser (904 nm) in the treatment of alopecia areata. 32
308-nm excimer laser for the treatment of alopecia areata. 32
Phase I/II randomized bilateral half-head comparison of topical bexarotene 1% gel for alopecia areata. 33
Comparison of azelaic acid and anthralin for the therapy of patchy alopecia areata: a pilot study. 33
Case reports: alopecia universalis: hair growth following initiation of simvastatin and ezetimibe therapy. 33
Hair growth in patients alopecia areata totalis after treatment with simvastatin and ezetimibe. 33
Randomized trial of aromatherapy. Successful treatment for alopecia areata. 33
Onion juice (Allium cepa L.), a new topical treatment for alopecia areata. 33
Combination of topical garlic gel and betamethasone valerate cream in the treatment of localised alopecia areata: a double-blinded randomised control study. 33
11 Amyloidosis 34
Management strategy 34
Specific investigations 34
First-Line therapies 34
Second-Line therapies 34
Comparative study of phototherapy (UVB) vs. photochemotherapy (PUVA) vs. topical steroids in the treatment of primary cutaneous lichen amyloidosis. 34
Successful treatment of lichen amyloidosis with combined bath PUVA photo-chemotherapy and oral acitretin. 35
Widespread biphasic amyloidosis: response to acitretin. 35
Excess tissue friability during CO2 laser vaporization of nodular amyloidosis. 35
A case of lichen amyloidosis treated with pulsed dye laser. 35
532-nm and 1064-nm Q-switched Nd : YAG laser therapy for reduction of pigmentation in macular amyloidosis patches. 35
The efficacy of dermabrasion in the treatment of nodular amyloidosis. 35
Lichen amyloidosis improved by 0.1% topical tacrolimus. 35
Transcutaneous electrical nerve stimulation for reduction of pruritus in macular amyloidosis and lichen simplex. 35
Clinical effect of tocoretinate on lichen and macular amyloidosis. 35
12 Androgenetic alopecia 36
Management strategy 36
Specific investigations for females 37
Hair loss in women. 37
Male and female pattern hair loss. 37
Hair through the female life cycle. 37
Medical therapies 37
Finasteride, 1 mg daily administration on male androgenetic alopecia in different age groups: 10-year follow-up. 37
Efficacy, safety, and tolerability of dutasteride 0.5 mg once daily in male patients with male pattern hair loss: a randomized, double-blind, placebo-controlled, phase III study. 37
A randomized, single-blind trial of 5% minoxidil foam once daily versus 2% minoxidil solution twice daily in the treatment of androgenetic alopecia in women. 37
Comparative efficacy of various treatment regimens for androgenetic alopecia in men. 37
Minoxidil versus finasteride in the treatment of men with androgenetic alopecia. 38
Treatment of female pattern hair loss with oral anti-androgens. 38
Efficacy and safety of finasteride therapy for androgenetic alopecia: a systematic review. 38
Surgical therapies 38
Planning and organization. 38
Follicular unit extraction. 38
Naturally occurring female hairline patterns. 38
Complications in hair restoration surgery. 38
The surgical treatment of cicatricial alopecia. 38
13 Angiolymphoid hyperplasia with eosinophilia 39
Management strategy 39
Specific investigations 39
Angiolymphoid hyperplasia with eosinophilia associated with pregnancy: a case report and review of the literature. 39
First-line therapies 39
Angiolymphoid hyperplasia with eosinophilia and vascular tumors of the head and neck. 39
Treatment of angiolymphoid hyperplasia with eosinophilia with the carbon dioxide laser. 39
Angiolymphoid hyperplasia with eosinophilia responsive to pulsed dye laser. 40
Angiolymphoid hyperplasia successfully treated with an ultralong pulsed dye laser. 40
Angiolymphoid hyperplasia with eosinophilia: successful treatment with the Nd : YAG laser. 40
Angiolymphoid hyperplasia with eosinophilia treated with vascular laser. 40
Second-line therapies 40
Angiolymphoid hyperplasia with eosinophilia successfully treated with imiquimod. A case report. 40
A case of angiolymphoid hyperplasia with eosinophilia successfully treated with tacrolimus ointment. 40
Angiolymphoid hyperplasia with eosinophilia: efficacy of isotretinoin? 40
Angiolymphoid hyperplasia with eosinophilia treated with a novel combination technique of radiofrequency ablation and sclerotherapy. 40
Third-line therapies 40
Angiolymphoid hyperplasia with eosinophilia responding to interferon-alpha 2B. 40
Angiolymphoid hyperplasia with eosinophilia treated with anti-interleukin-5 antibody (mepolizumab). 40
Angiolymphoid hyperplasia with eosinophilia: successful treatment with the antiallergic agent suplatast tosilate. 41
Angiolymphoid hyperplasia with eosinophilia: good response to photodynamic therapy. 41
Angiolymphoid hyperplasia with eosinophilia of the nail bed and bone: successful treatment with radiation therapy. 41
14 Angular cheilitis 42
Management strategy 42
Specific investigations 42
Angular cheilitis, part 1: local etiologies. 42
Angular cheilitis, part 2: nutritional, systemic, and drug-related causes and treatment. 42
Epidemiology and etiology of denture stomatitis. 42
Angular cheilitis. 42
Nickel-induced angular cheilitis due to orthodontic braces. 42
Down syndrome: lip lesions (angular stomatitis and fissures) and Candida albicans. 42
First-line therapies 42
Oral candidiasis and angular cheilitis. 42
Diseases of the lips. 43
The association between socioeconomic status, oral hygiene practice, denture stomatitis and oral status in elderly people living different residential homes. 43
Second-line therapies 43
15 Antiphospholipid syndrome 44
Management strategy 44
Specific investigations 44
International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). 45
Controversies and unresolved issues in antiphospholipid syndrome pathogenesis and management. 45
First-line therapies 45
Aspirin for primary thrombosis prevention in the antiphospholipid syndrome. 45
Comparison of two intensities of warfarin for the prevention of recurrent thrombosis in patients with the antiphospholipid syndrome. 45
A randomized clinical trial of high-intensity warfarin vs. conventional antithrombotic therapy for the prevention of recurrent thrombosis in patients with the antiphospholipid syndrome. 45
A systematic review of secondary thromboprophylaxis in patients with antiphospholipid antibodies. 45
Treatment of antiphospholipid antibody syndrome (APS) in pregnancy: a randomized pilot trial comparing low-molecular-weight heparin to unfractionated heparin. 45
Second-line therapies 45
Evidence-based management of thrombosis in the antiphospholipid antibody syndrome. 45
Effect of rituximab on clinical and laboratory features of antiphospholipid syndrome: a case report and review of literature. 45
A multicenter, placebo-controlled pilot study of intravenous immune globulin (IVIG) treatment of antiphospholipid syndrome during pregnancy. 45
Third-line therapies 45
Plasma exchange in the management of high risk pregnant patients with primary antiphospholipid syndrome. A report of 9 cases and a review of the literature. 46
Insertion of inferior vena cava filters in patients with the antiphospholipid syndrome. 46
Catastrophic antiphospholipid syndrome 46
Catastrophic antiphospholipid syndrome (CAPS): proposed guidelines for diagnosis and treatment. 46
Catastrophic antiphospholipid syndrome presenting with multiorgan failure and gangrenous lesions of the skin. 46
16 Aphthous stomatitis 47
Management strategy 47
Specific investigations 48
Aphthous ulcers. 48
Oral mucosal disease: recurrent aphthous stomatitis. 48
Haematological deficiencies in patients with recurrent aphthosis. 48
First-line therapies 48
Urban legends: recurrent aphthous stomatitis. 48
A controlled clinical trial of the efficacy of topically applied fluocinonide in the treatment of recurrent aphthous ulceration. 48
Topical corticosteroids in recurrent aphthous stomatitis. Systematic review. 48
Efficacy and safety of dexamethasone ointment on recurrent aphthous ulceration. 48
Treatment of aphthous ulcers in AIDS patients. 48
Amlexanox for the treatment of recurrent aphthous ulcers. 48
An evaluation of the efficacy and safety of amlexanox oral adhesive tablets in the treatment of recurrent minor aphthous ulceration in a Chinese cohort: a randomized, double- blind, vehicle-controlled, unparallel multicenter clinical trial. 48
Double-blind trial of tetracycline in recurrent aphthous ulceration. 48
Chlorhexidine gluconate mouthwash in the management of minor aphthous ulceration: a double-blind, placebo controlled cross-over trial. 48
Effect of an antimicrobial mouth rinse on recurrent aphthous ulcerations. 49
Mouth rinses containing triclosan reduce the incidence of recurrent aphthous ulcers (RAU). 49
Sucralfate suspension as a treatment of recurrent aphthous stomatitis. 49
Performance of a hydroxypropyl cellulose film former in normal and ulcerated mucosa. 49
Second-line therapies 49
Systemic treatment in severe cases of recurrent aphthous stomatitis: an open trial. 49
Comparison of colchicine versus prednisolone in recurrent aphthous stomatitis: a double-blind randomized clinical trial. 49
Successful treatment of complex aphthosis with colchicine and dapsone. 49
Clinical, historic, and therapeutic features of aphthous stomatitis: literature review and open trial employing steroids. 49
Prevention of recurrent aphthous stomatitis with colchicine: an open trial. 49
Thalidomide for the treatment of oral aphthous ulcers in patients with human immunodeficiency virus infection. 49
Refractory aphthous ulceration treated with thalidomide: a report of 10 years’ clinical experience. 49
Use of thalidomide for severe recurrent aphthous stomatitis: a multicenter cohort analysis. 50
The therapeutic and prophylactic role of oral zinc sulfate in management of recurrent aphthous stomatitis (ras) in comparison with dapsone. 50
Third-line therapies 50
A randomized, double-blind, placebo-controlled trial of pentoxifylline for the treatment of recurrent aphthous stomatitis. 50
Treatment of recurrent aphthous stomatitis with pentoxifylline. 50
Topical cyclosporine for oral mucosal disorders. 50
Chronic recurrent aphthous stomatitis: oral treatment with low-dose interferon alpha. 50
Aphthous ulcers responding to etretinate: a case report. 50
Managing aphthous ulcers: laser treatment applied. 50
Evaluation of penicillin G potassium troches in the treatment of minor recurrent aphthous ulceration in a Chinese cohort: a randomized, double-blinded, placebo and no-treatment-controlled, multicenter clinical trial. 50
Recalcitrant, recurrent aphthous stomatitis treated with etanercept. 50
Recalcitrant, recurrent aphthous stomatitis successfully treated with adalimumab. 50
Treatment of recurrent aphthous stomatitis with fumaric acid esters. 51
Treatment of recurrent aphthous stomatitis with clofazimine. 51
The effect of ascorbate on minor recurrent aphthous stomatitis. 51
Effectiveness of vitamin B12 in treating recurrent aphthous stomatitis: a randomized, double-blind, placebo controlled trial. 51
Silver nitrate cautery in aphthous stomatitis: a randomized controlled trial. 51
Pilot study on recurrent aphthous stomatitis (RAS): a randomized placebo-controlled trial for the comparative therapeutic effects of systemic prednisone and systemic montelukast in subjects unresponsive to topical therapy. 51
17 Atopic dermatitis 52
Management strategy 52
Interventional education 52
Skin care 52
Topical therapies 53
Other treatment considerations 53
Systemic therapies 54
Referral, quality of life issues, and educational resources 55
Hospitalization 55
Specific investigations 55
Management of atopic dermatitis in the pediatric population. 55
Guidelines for the diagnosis and management of food allergy in the United States: report of the NIAID-sponsored expert panel. 55
Seborrheic dermatitis-like and atopic dermatitis-like eruptions in HIV-infected patients. 55
First-line therapies 55
Age related, structured educational programmes for the management of atopic dermatitis in children and adolescents: multicentre, randomized controlled trial. 56
Psychological and educational interventions for atopic eczema in children. 56
Emollients improve treatment results with topical corticosteroids in childhood atopic dermatitis: a randomized comparative study. 56
Quantitative assessment of combination bathing and moisturizing regimens on skin hydration in atopic dermatitis. 56
Systematic review of treatments of atopic eczema. 56
Topical corticosteroids for atopic eczema: clinical and cost effectiveness of once-daily vs. more frequent use. 56
A systematic review of the safety of topical therapies for atopic dermatitis. 56
Efficacy and safety of wet-wrap dressings in children with severe atopic dermatitis: influence of corticosteroid dilution. 56
Wet dressing therapy in conjunction with topical corticosteroids is effective for rapid control of severe pediatric atopic dermatitis: experience with 218 patients over 30 years at Mayo Clinic. 56
Second-line therapies 56
Efficacy and safety of pimecrolimus cream in the long-term management of atopic dermatitis in children. 56
Safety and efficacy of pimecrolimus (ASM 981) cream 1% in the treatment of mild and moderate atopic dermatitis in children and adolescents. 56
0.03% Tacrolimus ointment applied once or twice daily is more efficacious than 1% hydrocortisone acetate in children with moderate to severe atopic dermatitis: results of a randomized double-blind controlled trial. 56
Sustained efficacy and safety of pimecrolimus cream 1% when used long-term (up to 26 weeks) to treat children with atopic dermatitis. 57
Intermittent therapy for flare prevention and long-term disease control in stabilized atopic dermatitis: a randomized comparison of 3-times-weekly applications of tacrolimus ointment versus vehicle. 57
Topical calcineurin inhibitors and malignancies in pediatric patients: a literature review. 57
Long-term efficacy and tolerability of tacrolimus 0.03% ointment in infants: a two-year open-label study. 57
Effects of cefuroxime axetil on Staphylococcus aureus colonization and superantigen production in atopic dermatitis. 57
Staphylococcus aureus: colonizing features and influence of an antibacterial treatment in adults with atopic dermatitis. 57
Children with atopic dermatitis appear less likely to be infected with community acquired methicillin-resistant Staphylococcus aureus: the San Diego experience. 57
An evidence-based review of the efficacy of antihistamines in relieving pruritus in atopic dermatitis. 57
A double-blinded, randomized, placebo-controlled trial of cetirizine in preventing the onset of asthma in children with atopic dermatitis: 18 months’ treatment and 18 months’ posttreatment follow-up. 57
Management of sleep disturbance associated with atopic dermatitis. 57
Ceramide-dominant barrier repair lipids alleviate childhood atopic dermatitis: changes in barrier function provide a sensitive indicator of disease activity. 57
New treatments for restoring impaired epidermal barrier permeability: skin barrier repair creams. 57
Third-line therapies 57
Double-blind controlled trial of effect of housedust-mite allergen avoidance on atopic dermatitis. 57
Rice nightmare: kwashiorkor in 2 Philadelphia-area infants fed Rice Dream beverage. 58
Probiotics during pregnancy and breast-feeding might confer immunomodulatory protection against atopic disease in the infant. 58
Probiotic supplementation for the first 6 months of life fails to reduce the risk of atopic dermatitis and increases the risk of allergen sensitization in high-risk children: a randomized controlled trial. 58
Effects of early nutritional interventions on the development of atopic disease in infants and children: the role of maternal dietary restriction, breastfeeding, timing of introduction of complementary foods, and hydrolyzed formulas. 58
The role of psoralen photochemotherapy (PUVA) in the treatment of severe atopic eczema in adolescents. 58
Phototherapy for atopic eczema with narrow-band UVB. 58
Half-side comparison study on the efficacy of 8-methoxy-psoralen bath-PUVA versus narrow-band ultraviolet B phototherapy in patients with severe chronic atopic dermatitis. 58
Long-term efficacy of medium-dose UVA1 phototherapy in atopic dermatitis. 58
Phototherapy in the management of atopic dermatitis: a systematic review. 58
Azathioprine in severe adult atopic dermatitis: a double-blind, placebo-controlled, crossover trial. 58
A retrospective evaluation of azathioprine in severe childhood atopic eczema, using thiopurine methyltransferase levels to exclude patients at high risk of myelosuppression. 58
Parallel-group randomized controlled trial of azathioprine in moderate to severe atopic eczema, using a thiopurine methyltransferase-based dose regimen. 58
Efficacy and tolerability at 3 and 6 months following use of azathioprine for recalcitrant atopic dermatitis in children and young adults. 58
Systemic treatment of pediatric atopic dermatitis with azathioprine and mycophenolate mofetil. 58
Oral azathioprine for recalcitrant pediatric atopic dermatitis: clinical response and thiopurine monitoring. 59
Cyclosporine in the treatment of patients with atopic eczema – a systematic review and meta-analysis. 59
Double-blind, controlled, crossover study of cyclosporine in adults with severe refractory atopic dermatitis. 59
Cyclosporine greatly improves the quality of life of adults with severe atopic dermatitis. 59
Cyclosporine in atopic dermatitis: time to relapse and effect of intermittent therapy. 59
Long-term efficacy and safety of cyclosporine in severe adult atopic dermatitis. 59
Cyclosporine in atopic dermatitis: review of the literature and outline of a Belgian consensus. 59
An open-label, dose-ranging study of methotrexate for moderate-to-severe adult atopic eczema. 59
A randomized trial of methotrexate versus azathioprine for severe atopic eczema. 59
Treatment of atopic eczema with oral mycophenolate mofetil. 59
Mycophenolate mofetil for severe childhood atopic dermatitis: experience in 14 patients. 59
Enteric-coated mycophenolate sodium versus cyclosporin A as long-term treatment in adult patients with severe atopic dermatitis: a randomized controlled trial. 59
Recombinant interferon gamma therapy for atopic dermatitis. 60
Long-term effectiveness and safety of recombinant human interferon gamma therapy for atopic dermatitis despite unchanged serum IgE levels. 60
Do some patients with atopic dermatitis require long term oral steroid therapy? 60
18 Atypical nevi 61
Management strategy 61
Specific investigations 62
Handbook of dermoscopy. 62
Atlas of dermoscopy. 62
Color atlas of melanocytic lesions of the skin. 62
Variables predicting change in benign melanocytic nevi undergoing short-term dermoscopic imaging. 62
Impact of digital dermoscopy analysis on the decision to follow up or to excise a pigmented skin lesion: a multicentre study. 62
Impact of dermoscopy on the management of high-risk patients from melanoma families: a prospective study. 62
In vivo confocal microscopy for detection and grading of dysplastic nevi: a pilot study. 63
Application of mobile teledermatology for skin cancer screening. 63
First-line therapies 63
A decade of melanomas: identification of factors associated with delayed detection in an academic group practice. 63
The number of benign moles excised for each malignant melanoma: the number needed to treat. 63
Revised U.K. guidelines for the management of cutaneous melanoma. 63
Dysplastic naevi: to shave, or not to shave? A retrospective study of the use of the shave biopsy technique in the initial management of dysplastic naevi. 63
Clinical decision making based on histopathologic grading and margin status of dysplastic nevi. 64
19 Autoimmune progesterone dermatitis 65
Management strategy 65
Specific investigations 65
The role of intradermal skin testing and patch testing in the diagnosis of autoimmune progesterone dermatitis. 65
Autoimmune progesterone dermatitis and its manifestation as anaphylaxis: a case report and literature review. 65
20 Bacillary angiomatosis 68
Management strategy 68
Specific investigations 68
Laboratory diagnosis of Bartonella infections. 69
Bacillary angiomatosis and bacillary peliosis in patients infected with human immunodeficiency virus: clinical characteristics in a case–control study. 69
Bacillary angiomatosis in immunocompromised patients. 69
Culture of Bartonella quintana and Bartonella henselae from human samples: a 5-year experience (1993 to 1998). 69
Rapid identification and differentiation of Bartonella species using a single step PCR assay. 69
Use of Bartonella adhesin A (BadA) immunoblotting in the serodiagnosis of Bartonella henselae infections. 69
First-line therapies 69
Molecular epidemiology of Bartonella infections in patients with bacillary angiomatosis-peliosis. 69
MICs of 28 antibiotic compounds for 14 Bartonella (formerly Rochalimaea) isolates. 69
AIDS commentary: bacillary angiomatosis and bacillary peliosis in patients infected with human immunodeficiency virus. 69
Bacillary angiomatosis in an immunocompetent child: a case report and review of the literature. 69
Molecular diagnosis of deep nodular bacillary angiomatosis and monitoring of therapeutic success. 69
Recommendations for the treatment of human infections caused by Bartonella species. 69
Second-line therapies 69
Clarithromycin therapy for bacillary peliosis did not prevent bacillary angiomatosis. 69
Bacillary angiomatosis: presentation of six patients, some with unusual features. 70
Third-line therapies 70
Bacillary angiomatosis in a pregnant patient with acquired immunodeficiency syndrome. 70
Lack of bactericidal effect of antibiotics except aminoglycosides on Bartonella (Rochalimaea) henselae. 70
Cutaneous bacillary angiomatosis in renal transplant recipients: report of three new cases and literature review. 70
21 Balanitis 71
Management strategy 71
Specific investigations 71
Mild balanoposthitis. 71
Balanitis and balanoposthitis: a review. 71
European guideline for the management of balanoposthitis. 71
Noninfectious penile lesions. 71
First-Line therapies 72
Clinical features and management of recurrent balanitis: association with atopy and genital washing. 72
Second-Line therapies 72
Candida balanitis: risk factors. 72
Lichen sclerosus: review of the literature and current recommendations for management. 72
British Association of Dermatologists’ guidelines for the management of lichen sclerosus 2010. 72
Penile lichen sclerosus treated with clobetasol dipropionate 0.05% cream: a retrospective clinical and histopathological study. 72
The response of balanitis xerotica obliterans to local steroid application compared with placebo in children. 72
Conservative treatment of phymosis with fluticasone proprionate 0.05%: a clinical study in 1185 boys. 72
Plasma cell balanitis of Zoon: response to Trimovate cream. 72
Lichen sclerosus of the male genitalia and urethra: surgical options and results in a multicenter international experience with 215 patients. 72
Plasma cell balanitis: clinical and histopathological features – response to circumcision. 72
Plasma cell balanitis: clinicopathologic study of 112 cases and treatment modalities. 72
Third-Line therapies 72
Multicentre, phase II trial on the safety and efficacy of topical tacrolimus ointment for the treatment of lichen sclerosus. 72
Safety and tolerability of adjuvant topical tacrolimus treatment in boys with lichen sclerosus: a prospective phase 2 study. 73
Plasma cell balanitis of Zoon treated with topical tacrolimus 0.1%: report of 3 cases. 73
Topical tacrolimus: an effective therapy for Zoon balanitis. 73
Pimecrolimus 1% cream in non-specific inflammatory recurrent balanitis. 73
Two cases of Zoon’s balanitis treated with pimecrolimus 1% cream. 73
Zoon’s balanitis treated with imiquimod 5% cream. 73
Ablative erbium : YAG laser treatment of idiopathic chronic inflammatory non-cicatricial balanoposthitis (Zoon’s disease). A series of 20 patients with long-term outcome. 73
Genital lichen sclerosus treated by carbon dioxide laser. 73
Zoon’s balanitis: presentation of 15 patients, five treated with a carbon dioxide laser. 73
22 Basal cell carcinoma 74
Management strategy 74
Specific investigations 74
Subsequent primary cancers after basal-cell carcinoma: a nationwide study in Finland from 1953 to 1995. 75
Basal cell carcinoma and risk of subsequent malignancies: a cancer registry-based study in southwest England. 75
Are patients with skin cancer at lower risk of developing colorectal or breast cancer? 75
First-Line therapies 75
Recurrence rates of treated basal cell carcinomas. Part 2: curettage–electrodesiccation. 75
Long term recurrence rates in previously untreated (primary) basal cell carcinoma: implications for patient follow-up. 75
Mohs surgery is the treatment of choice for recurrent (previously treated) basal cell carcinoma. 75
Cryosurgery of basal cell carcinoma: a study of 358 patients. 75
A systematic review of treatment modalities for primary basal cell carcinomas. 75
Surgical margins for basal cell carcinoma. 75
Morpheaform basal-cell epitheliomas: a study of subclinical extensions in a series of 51 cases. 75
Efficacy of curettage before excision in clearing surgical margins of nonmelanoma skin cancer. 75
Long-term recurrence rates in previously untreated (primary) basal cell carcinoma: implications for patient follow-up. 76
Mohs surgery is the treatment of choice for recurrent (previously treated) basal cell carcinoma. 76
Surgical excision vs Mohs’ micrographic surgery for basal-cell carcinoma of the face: randomized controlled trial. 76
Second-Line therapies 76
Basal cell carcinoma of the face: surgery or radiotherapy? Results of a randomized study. 76
Therapeutic ionizing radiation and the incidence of basal cell carcinoma and squamous cell carcinoma. 76
Third-Line therapies 76
Intralesional interferon therapy for basal cell carcinoma. 76
Intralesional recombinant interferon beta-1a in the treatment of basal cell carcinoma: results of an open-label multicentre study. 76
Treatment and prevention of basal cell carcinoma with oral isotretinoin. 76
Topical tretinoin treatment in basal cell carcinoma. 76
Topical treatment of basal cell carcinoma with tazarotene: a clinicopathological study on a large series of cases. 77
Imiquimod 5% cream for the treatment of superficial basal cell carcinoma: results from two phase III, randomized, vehicle-controlled studies. 77
Open study of the efficacy and mechanism of action of topical imiquimod in basal cell carcinoma. 77
Photodynamic therapy for the treatment of basal cell carcinoma. 77
Photodynamic therapy of multiple nonmelanoma skin cancers with verteporfin and red light-emitting diodes: two year results evaluating tumor response and cosmetic outcomes. 77
Five year follow-up of a randomized prospective trial of topical methyl aminolevulinate photodynamic therapy vs. surgery for nodular basal cell carcinoma. 77
Treatment of basal cell carcinoma of the skin with 5-fluorouracil ointment. A 10 year follow-up study. 77
Fluorouracil paste treatment of thin basal cell carcinomas. 77
5% 5-fluorouracil cream for the treatment of small superficial basal cell carcinoma: efficacy, tolerability, cosmetic outcome, and patient satisfaction. 77
Can the carbon dioxide laser completely ablate basal cell carcinomas? A histological study. 77
Effect of perilesional injections of PEG–interleukin-2 from one dose a week to four doses a week. 78
Nonsteroidal anti-inflammatory drugs and the risk of skin cancer: a population-based case-control study. 78
PEP005 (ingenol mebutate) gel for the topical treatment of superficial basal cell carcinoma: results of a randomized phase IIa trial. 78
Inhibition of the hedgehog pathway in advanced basal-cell carcinoma. 78
Targeting superficial or nodular basal cell carcinoma with topically formulated small molecule inhibitor of smoothened. 78
23 Becker’s nevus 79
Management strategy 79
Becker’s nevus syndrome revisited. 79
Becker nevus syndrome. 79
Becker’s nevus and malignant melanoma. 79
A case of Becker’s nevus with osteoma cutis. 79
Specific investigations 79
Familial Becker’s nevus. 79
Dermoscopic features of congenital melanocytic nevus and Becker nevus in an adult male population: an analysis with a 10-fold magnification. 80
First-line therapies 80
24 Bed bugs 82
Management strategy 82
Insecticide resistance in the bed bug: a factor in the pest’s sudden resurgence? 83
Acute illnesses associated with insecticides used to control bed bugs – seven states, 2003–2010. 83
Identification of the airborne aggregation pheromone of the common bed bug, Cimex lectularius. 83
Wolbachia as a bacteriocyte-associated nutritional mutualist. 83
Bedbugs as vectors for drug-resistant bacteria [letter]. 83
Bedbugs. 83
Specific investigations 83
Visual inspection 83
Canine inspection 84
Bed bug traps 84
Other monitoring devices 84
Skin biopsy 84
Ability of bed bug-detecting canines to locate live bed bugs and viable bed bug eggs. 84
Effectiveness of bed bug monitors for detecting and trapping bed bugs in apartments. 84
First-line therapies 84
Bullous reactions to bedbug bites reflect cutaneous vasculitis. 84
25 Behçet disease 85
Management strategy 85
Specific investigations 85
Behçet’s syndrome: immunopathological and histopathological assessment of pathergy lesions is useful in diagnosis and follow-up. 85
Behçet’s disease and complex aphthosis. 85
Evaluation of current therapeutic strategies in Behçet’s disease. 85
First-line therapies 85
Management of Behçet’s disease: a systematic literature review for the European League Against Rheumatism evidence-based recommendations for the management of Behçet’s disease. 85
A double-blind trial of colchicine in Behçet’s syndrome. 86
Recurrent aphthous stomatitis: treatment with colchicine. An open trial of 54 cases. 86
Oral zinc sulfate in the treatment of Behçet’s disease: a double blind cross-over study. 86
Pimecrolimus versus placebo in genital aphthous ulcers of Behçet’s disease: a randomized double-blind controlled trial. 86
Second-line therapies 86
Dapsone in Behçet’s disease: a double-blind, placebo-controlled, cross-over study. 86
Thalidomide in the treatment of the mucocutaneous lesions of Behçet syndrome: a randomized, double-blind, placebo-controlled trial. 86
Low-dose weekly methotrexate for unusual neutrophilic vascular reactions: cutaneous polyarteritis nodosa and Behçet’s disease. 86
Practical treatment recommendations for pharmacotherapy of Behçet’s syndrome. 86
Third-line therapies 86
Successful treatment of Behçet’s disease with lenalidomide. 86
Differential efficacy of human recombinant interferon-alpha2a on ocular and extraocular manifestations of Behçet disease: results of an open 4-center trial. 86
Interferon alfa-2a in the treatment of Behçet disease: a randomized placebo-controlled and double-blind study. 87
Interferon-alpha treatment of Behçet’s disease. 87
Systemic isotretinoin in the treatment of a Behçet’s patient with arthritic symptoms and acne lesions. 87
Double-masked trial of cyclosporine versus colchicine and long-term open study of cyclosporine in Behçet’s disease. 87
Cyclosporine in Behçet’s disease: results in 16 patients after 24 months of therapy. 87
Efficacy of cyclosporine on mucocutaneous manifestations of Behçet’s disease. 87
A controlled trial of azathioprine in Behçet’s syndrome. 87
High-dose cyclophosphamide without stem cell rescue for the treatment of refractory Behçet’s disease. 87
Long-lasting remission of Behçet’s disease after chlorambucil therapy. 87
Streptococcal infection in the pathogenesis of Behçet’s disease and clinical effects of minocycline on the disease symptoms. 87
Oral prostaglandin E1 as a therapeutic modality for leg ulcers in Behçet’s disease. 87
Efficacy of rebamipide as adjunctive therapy in the treatment of recurrent oral aphthous ulcers in patients with Behçet’s disease. 87
Short-term trial of etanercept in Behçet’s disease: a double blind, placebo controlled study. 87
Infliximab for the treatment of resistant oral ulcers in Behçet’s disease: a case report and review of the literature. 87
Infliximab treatment for ocular and extraocular manifestations of Behçet’s disease. 87
Anti-TNF agents for Behçet’s disease: analysis of published data on 369 patients. 88
Remission induction in Behçet’s disease following lymphocyte depletion by the anti-CD52 antibody CAMPATH 1-H. 88
Treatment of Behçet’s disease with granulocyte and monocyte adsorption apheresis. 88
Clinical and immunological effects of azithromycin in Behçet’s disease. 88
Effect of prophylactic benzathine penicillin on mucocutaneous symptoms of Behçet’s disease. 88
Behçet’s disease: remission of patient symptoms after oral contraceptive therapy. 88
Nicotine-patch therapy of mucocutaneous lesions of Behçet’s disease: a case series. 88
Mycophenolate sodium in the treatment of mucocutaneous Behçet’s disease. 88
26 Bioterrorism 89
Smallpox 89
Management strategy 89
Specific investigations 89
Laboratory diagnosis to differentiate smallpox, vaccinia, and other vesicular/pustular illnesses. 89
Cutaneous manifestations of category A bioweapons. 90
Development and experience with an algorithm to evaluate suspected smallpox cases in the United States, 2002–2004. 90
First-line therapies 90
Countermeasures and vaccination against terrorism using smallpox: pre-event and post-event smallpox vaccination and its contraindications. 90
Inactivation of poxviruses by upper-room UVC light in a simulated hospital room environment. 90
Vaccinia virus infection after sexual contact with a military smallpox vaccinee. 90
Progressive vaccinia in a military smallpox vaccinee: United States, 2009. 90
Household transmission of vaccinia virus from contact with a military smallpox vaccinee: Illinois and Indiana, 2007. 90
A randomized, double-blind, dose-finding phase II study to evaluate immunogenicity and safety of the third generation smallpox vaccine candidate IMVAMUNE. 90
Electrocardiography screening for cardiotoxicity after modified Vaccinia Ankara vaccination. 90
Adverse events following smallpox vaccination with ACAM2000 in a military population. 90
Clinical efficacy of intramuscular Vaccinia immune globulin: a literature review. 90
Ocular complications in the Department of Defense Smallpox Vaccination Program. 91
Pregnancy discovered after smallpox vaccination: is vaccinia immune globulin appropriate? 91
Myopericarditis following smallpox vaccination among vaccinia-naive US military personnel. 91
Mucosal immunization induces a higher level of lasting neutralizing antibody response in mice by a replication-competent smallpox vaccine: vaccinia Tiantan strain. 91
Traditional smallpox vaccination with reduced risk of inadvertent contact spread by administration of povidone iodine ointment. 91
Second-line therapies 91
Third-line therapies 91
Severe eczema vaccinatum in a household contact of a smallpox vaccinee. 91
Cidofovir in the treatment of poxvirus infections. 91
Cutaneous infections of mice with vaccinia or cowpox viruses and efficacy of cidofovir. 91
Anthrax 91
Management strategy 92
Specific investigations 92
Cutaneous manifestations of category A bioweapons. 92
Anthrax infection. 92
An overview of anthrax infection including the recently identified form of disease in injection drug users. 92
Detection technologies for Bacillus anthracis: prospects and challenges. 92
First-line therapies 92
Conference report on public health and clinical guidelines for anthrax. 92
Anthrax prevention and treatment: utility of therapy combining antibiotic plus vaccine. 92
Raxibacumab [treatment of inhalation anthrax]. 92
Second-line therapies 92
Amoxicillin for postexposure inhalational anthrax in pediatrics: rationale for dosing recommendations. 92
Raxibacumab for the treatment of inhalational anthrax. 92
Third-line therapies 93
Novel approaches to the treatment of systemic anthrax. 93
A dual-purpose protein ligand for effective therapy and sensitive diagnosis of anthrax. 93
Prophylaxis 93
Use of anthrax vaccine in the U.S.: recommendations of the Advisory Committee on Immunization Practices (ACIP). 93
A short course of antibiotic treatment is effective in preventing death from experimental inhalational anthrax after discontinuing antibiotics. 93
Tularemia 93
Management strategy 93
Specific investigations 93
Clinical and laboratory findings of tularemia: a retrospective analysis. 94
WHO guidelines on tularaemia. 94
27 Bites and stings 96
Management strategy 96
Bite reactions 96
Anaphylaxis 96
Vector-borne disease 96
Specific investigations 96
Allergy blood testing: a practical guide for clinicians. 96
Causes of ant sting anaphylaxis in Australia: the Australian Ant Venom Allergy Study. 96
Detection of West Nile virus genome and specific antibodies in Iranian encephalitis patients. 96
Molecular characterization of Swiss Ceratopogonidae (Diptera) and evaluation of real-time PCR assays for the identification of Culicoides biting midges. 96
Usefulness of post mortem determination of serum tryptase, histamine and diamine oxidase in the diagnosis of fatal anaphylaxis. 96
First-line therapy 97
Tick bite protection with permethrin-treated summer-weight clothing. 97
Pilot study assessing the effectiveness of long-lasting permethrin-impregnated clothing for the prevention of tick bites. 97
Synergistic insecticidal and repellent effects of combined pyrethroid- and repellent-impregnated bed nets using a novel long-lasting polymer-coating multi-layer technique. 97
Collapse of Anopheles darlingi populations in Suriname after introduction of insecticide-treated nets (ITNs): malaria down to near elimination level. 97
Impact of insecticide-treated bed nets on malaria transmission indices on the south coast of Kenya. 97
Malaria morbidity and pyrethroid resistance after the introduction of insecticide-treated bednets and artemisinin-based combination therapies: a longitudinal study. 97
Scorpion envenomations in young children in central Arizona. 97
Utility of scorpion antivenin vs prazosin in the management of severe Mesobuthus tamulus (Indian red scorpion) envenoming at rural setting. 98
Safety of Hymenoptera venom immunotherapy: a systematic review. 98
Second-line therapies 98
The use of concentrated heat after insect bites/stings as an alternative to reduce swelling, pain, and pruritus: an open cohort-study at German beaches and bathing-lakes. 98
Field evaluation of commercial repellents against the floodwater mosquito Psorophora columbiae (Diptera: Culicidae) in St. Johns County, Florida. 98
Larval source management for malaria control in Africa: myths and reality. 98
The biological activity of a novel pyrethroid: metofluthrin. 98
Third-line therapies 98
Potential of the bush mint, Hyptis suaveolens essential oil for personal protection against mosquito biting. 98
Repellent plants provide affordable natural screening to prevent mosquito house entry in tropical rural settings: results from a pilot efficacy study. 99
An ethnobotanical survey of mosquito repellent plants in uMkhanyakude district, KwaZulu-Natal province, South Africa. 99
Efficacy of Advanced Odomos repellent cream (N, N-diethyl-benzamide) against mosquito vectors. 99
Repellent activity of plant essential oils against bites of Lutzomyia migonei (Diptera: Psychodidae). 99
Captopril in the treatment of cardiovascular manifestations of indian red scorpion (Mesobuthus tamulus concanesis Pocock) envenomation. 99
28 Blastomycosis 100
Management strategy 100
Specific investigations 100
Cutaneous inoculation blastomycosis. 100
First-line therapies 100
Blastomycosis. 100
Itraconazole therapy for blastomycosis and histoplasmosis. 101
Endemic blastomycosis in Mississippi: epidemiological and clinical studies. 101
Blastomycosis of the central nervous system: a multicenter review of diagnosis and treatment in the modern era. 101
Second-line therapies 101
Treatment of blastomycosis and histoplasmosis with ketoconazole. Results of a prospective randomized clinical trial. 101
Treatment of blastomycosis with fluconazole: a pilot study. 101
Treatment of blastomycosis with higher doses of fluconazole. 101
The role of voriconazole in the treatment of central nervous system blastomycosis. 101
Voriconazole use for endemic fungal infections. 101
Treatment of chronic pulmonary blastomycosis with caspofungin. 101
Guidelines 101
Clinical practice guidelines for the management of blastomycosis: 2008 update by the Infectious Diseases Society of America. 101
29 Blistering distal dactylitis 103
Management strategy 103
Specific investigations 103
A clinically recognizable streptococcal infection. 103
Staphylococcal blistering dactylitis: a case series in children under nine months of age. 103
First-line therapies 103
Is blistering distal dactylitis a variant of bullous impetigo? 103
Second-line therapies 103
Blistering distal dactylitis: a manifestation of group A beta-haemolytic streptococcal infection. 103
MRSA blistering distal dactylitis and review of reported cases. 103
Third-line therapies 103
A review and report of blistering distal dactylitis due to Staphylococcus aureus in two HIV-positive men. 103
Coexistent infections on a child’s distal phalanx: blistering dactylitis and herpetic whitlow. 103
30 Body dysmorphic disease (dermatologic nondisease) 104
Management strategy 104
Specific investigations 104
Depression, anxiety, anger, and somatic symptoms in patients with body dysmorphic disorder. 104
Development of a cosmetic procedure screening questionnaire (COPS) for body dysmorphic disorder. 104
A screening questionnaire for body dysmorphic disorder in a cosmetic dermatologic surgery practice. 105
First-line therapies 105
The Broken Mirror: Understanding and Treating Body Dysmorphic Disorder. 105
Obsessive-compulsive disorder: Core interventions in the treatment of obsessive-compulsive disorder and body dysmorphic disorder. 105
The Diagnostic and Statistical Manual for Mental Disorders 5th edition. 105
Body dysmorphic disorder: A treatment manual. 105
A randomized placebo-controlled trial of fluoxetine in body dysmorphic disorder. 105
BDD: a CBT model and pilot RCT. 105
Cognitive behavioural body image therapy for BDD. 105
Second-line therapies 105
Pharmacologic treatment of body dysmorphic disorder: A review of the evidence and a recommended treatment approach. 105
The dysmorphic syndrome. 105
31 Bowen’s disease and erythroplasia of Queyrat 106
Management strategy 106
Specific investigations 106
Dermoscopy of Bowen’s disease. 106
The prevalence of human papillomavirus genotypes in nonmelanoma skin cancers of nonimmunosuppressed individuals identifies high-risk genital types as possible risk factors. 106
First-line therapies 106
Cutaneous squamous carcinoma in situ (Bowen’s disease): treatment with Mohs micrographic surgery. 106
Bowen’s disease involving the urethra. 106
Extensive Bowen’s disease of the penile shaft treated with fresh tissue Mohs micrographic surgery in two separate operations. 106
Second-line therapies 106
Comparison of cryotherapy with curettage in the treatment of Bowen’s disease: a prospective study. 106
Curettage-cryosurgery for non-melanoma skin cancer of the external ear: excellent 5-year results. 106
Third-line therapies 107
Topical treatment of Bowen’s disease with 5-fluorouracil. 107
Comparison of topical methyl aminolevulinate photodynamic therapy with cryotherapy or fluorouracil for treatment of squamous cell carcinoma in situ. 107
Guidelines on the use of photodynamic therapy for nonmelanoma skin cancer: an international consensus. 107
Photodynamic therapy with methyl aminolevulinate for atypical carcinoma in situ of the penis. 107
Imiquimod 5% cream monotherapy for cutaneous squamous cell carcinoma in situ (Bowen’s disease): a randomized, double-blind, placebo-controlled trial. 107
Treatment of Bowen’s disease with topical 5% imiquimod cream: retrospective study. 107
Cryoimmunotherapy: superficial basal cell cancer and squamous cell carcinoma in situ treated with liquid nitrogen followed by imiquimod. 107
Erythroplasia of Queyrat treated with imiquimod 5% cream. 107
Radiation therapy for Bowen’s disease of the skin. 107
Concomitant use of a high-energy pulsed CO2 laser and a long-pulsed (810 nm) diode laser for squamous cell carcinoma in situ. 107
Treatment of multiple lesions of Bowen’s disease with iso-tretinoin and interferon alpha. 107
32 Bullous pemphigoid 108
Management strategy 108
Specific investigations 108
Drug-induced pemphigoid: bullous and cicatricial. 108
Prediction of survival for patients with bullous pemphigoid: a prospective study. 109
Increased frequency of diabetes mellitus in patients with bullous pemphigoid: a case–control study. 109
Antiphospholipid antibodies in patients with autoimmune blistering disease. 109
First-line therapies 109
A comparison of oral and topical corticosteroids in patients with bullous pemphigoid. 109
A comparison of two regimens of topical corticosteroids in the treatment of patients with bullous pemphigoid: a multicenter randomized study. 109
Treatment of bullous pemphigoid with prednisolone only: 0.75 mg/kg/day versus 1.25 mg/kg/day. A multicenter randomized study. 109
Nicotinamide and tetracycline therapy of bullous pemphigoid. 109
Minocycline as a therapeutic option in bullous pemphigoid. 109
Generalized bullous pemphigoid controlled by tetracycline therapy alone. 109
Second-line therapies 109
Azathioprine in the treatment of bullous pemphigoid. 109
Azathioprine plus prednisone in treatment of pemphigoid. 109
A comparison of oral methylprednisolone plus azathioprine or mycophenolate mofetil for the treatment of bullous pemphigoid. 109
Dapsone as first line therapy for bullous pemphigoid. 110
Combined treatment with low-dose methotrexate and initial short-term superpotent topical steroids in bullous pemphigoid: an open, multicentre, retrospective study. 110
Low-dose methotrexate treatment in elderly patients with bullous pemphigoid. 110
Low-dose oral pulse methotrexate as monotherapy in elderly patients with bullous pemphigoid. 110
Third-line therapies 110
Consensus statement on the use of intravenous immunoglobulin therapy in the treatment of autoimmune mucocutaneous blistering diseases. 110
Chlorambucil as a steroid-sparing agent in bullous pemphigoid. 110
High-dose methylprednisolone in the treatment of bullous pemphigoid. 110
Severe bullous pemphigoid responsive to pulsed intravenous dexamethasone and oral cyclophosphamide. 110
Successful treatment of bullous pemphigoid with pulsed intravenous cyclophosphamide. 110
Effects of cyclosporine on bullous pemphigoid and pemphigus. 110
Treatment of coexisting bullous pemphigoid and psoriasis with the tumor necrosis factor antagonist etanercept. 110
Rituximab for treatment-refractory pemphigus and pemphigoid: a case series of 17 patients. 110
Bullous and mucous membrane pemphigoid show a mixed response to rituximab: experience in seven patients. 111
Daclizumab: a novel therapeutic option in severe bullous pemphigoid. 111
Pathogenecity of IgE in autoimmunity: successful treatment of bullous pemphigoid with omalizumab. 111
Successful management of severe infant bullous pemphigoid with omalizumab. 111
33 Burning mouth syndrome (glossodynia) 112
Management strategies 112
Local factors 112
Systemic factors 112
Psychological factors 112
Specific investigations 112
Pathophysiology of primary burning mouth syndrome. 113
Psychiatric comorbidity in patients with burning mouth syndrome. 113
Interventions for the treatment of burning mouth syndrome. 113
Clinical assessment and outcome in 70 patients with complaints of burning or sore mouth symptoms. 113
Burning mouth syndrome: an update. 113
Burning mouth syndrome. 113
First-line therapies 113
Patients complaining of a burning mouth. Further experience in clinical assessment and management. 113
Glossodynia from Candida-associated lesions, burning mouth syndrome, or mixed causes. 113
Drug-induced burning mouth syndrome: a new etiological diagnosis. 113
Proton pump inhibitors. 113
Topirimate-induced burning mouth syndrome. 113
Zinc deficiency may be a cause of burning mouth syndrome as zinc replacement therapy has therapeutic effects. 113
Second-line therapies 113
Application of a capsaicin rinse in the treatment of burning mouth syndrome. 114
Capsaicin in burning mouth syndrome: titration strategies. 114
Topical clonazepam in stomatodynia: a randomised placebo-controlled study. 114
A double-blind study on clonazepam in patients with burning mouth syndrome. 114
Outcome predictors affecting the efficacy of clonazepam therapy for the management of burning mouth syndrome (BMS). 114
Management of burning mouth syndrome. 114
Oral medicine in practice: burning mouth syndrome. 114
An open-label, noncomparative, dose escalation pilot study of the effect of paroxetine in treatment of burning mouth syndrome. 114
Milnacipran dose–effect study in patients with burning mouth syndrome. 114
Marked response of burning mouth syndrome to pregabalin treatment. 114
Gabapentin has little or no effect in the treatment of burning mouth syndrome: results of an open-label pilot study. 114
Burning mouth syndrome responsive to duloxetine: a case report. 114
Two cases of burning mouth syndrome treated with olanzapine. 114
Lack of efficacy of alpha-lipoic acid in burning mouth syndrome: a double-blind, randomized, placebo-controlled study. 114
Alpha lipoic acid in burning mouth syndrome: a randomized double-blind placebo-controlled trial. 114
Cognitive therapy in the treatment of patients with resistant burning mouth syndrome: a controlled study. 114
Third-line therapies 114
The burning mouth syndrome. 114
Type 3 burning mouth syndrome: psychological and allergic aspects. 114
Group psychotherapy: an additional approach to burning mouth syndrome. 114
Treatment of burning mouth syndrome with a low-level energy diode laser. 115
34 Calcinosis cutis 116
Management strategy 116
Specific investigations 116
First-line therapies 116
Self-healing dystrophic calcinosis following trauma with transepidermal elimination. 116
Large subcutaneous calcification in systemic lupus erythematosus: treatment with oral aluminium hydroxide administration followed by surgical excision. 116
Calcinosis cutis in juvenile dermatomyositis responsive to aluminum hydroxide treatment. 117
Cutaneous calcinosis of scleroderma. Successful treatment with intralesional adrenal steroids. 117
Calcinosis cutis occurring in association with autoimmune connective tissue disease: the Mayo Clinic experience with 78 patients, 1996–2009. 117
Calcinosis cutis: part II. Treatment options. 117
A case of juvenile dermatomyositis with severe calcinosis and successful treatment with prednisone and diltiazem. 117
Second-line therapies 117
Effectiveness of the treatment with intravenous pamidronate in calcinosis in juvenile dermatomyositis. 117
New insight into calcinosis of juvenile dermatomyositis: a study of composition and treatment. 117
Efficacy of probenecid for a patient with juvenile dermatomyositis complicated with calcinosis. 117
Calcinosis universalis complicating juvenile dermatomyositis: resolution during probenecid therapy. 117
Treatment of cutaneous calcinosis in limited systemic sclerosis with minocycline. 117
Third-line therapies 117
Low dose warfarin treatment for calcinosis in patients with systemic sclerosis. 118
Treatment of systemic sclerosis-associated calcinosis: a case report of rituximab-induced regression of CREST-related calcinosis and review of the literature. 118
Calcinosis cutis associated with amyopathic dermatomyositis: response to intravenous immunoglobulin. 118
Response of dystrophic calcification to intravenous immunoglobulin. 118
Successful treatment of severe iatrogenic calcinosis cutis with intravenous sodium thiosulfate in a child affected by T-acute lymphoblastic leukemia. 118
A novel treatment for ulcerative calcinosis cutis. 118
Surgical debridement of painful fingertip calcinosis cutis in CREST syndrome. 118
Successful palliation and significant remission of cutaneous calcinosis in CREST syndrome with carbon dioxide laser. 118
Therapy of calcinosis cutis using erbium-doped yttrium aluminum garnet laser treatment. 118
Treatment of calcinosis cutis by extracorporeal shock-wave lithotripsy. 118
35 Calciphylaxis 119
Management strategy 119
Specific investigations 119
Pathogenesis of calciphylaxis: Hans Selye to nuclear factor kappa-B. 119
First-line therapies 119
Calcium use increases risk of calciphylaxis: a case-control study. 119
Risk factors and mortality associated with calciphylaxis in end-stage renal disease. 120
Calciphylaxis: natural history, risk factor analysis, and outcome. 120
The evolving pattern of calciphylaxis: therapeutic considerations. 120
Sodium thiosulfate as first-line treatment for calciphylaxis. 120
Calciphylaxis is usually non-ulcerating: risk factors, outcome and therapy. 120
Proximal calciphylaxis treated with calcimimetic ‘Cinacalcet’. 120
Rapid improvement of calciphylaxis after intravenous pamidronate therapy in a patient with chronic renal failure. 120
Multi-intervention management of calciphylaxis: a report of 7 cases. 120
Second-line therapies 120
Calciphylaxis: a syndrome of skin necrosis and acral gangrene in chronic renal failure. 120
Hyperbaric oxygen in the treatment of calciphylaxis: a case series. 120
Successful treatment of severe calciphylaxis in a hemodialysis patient using low-calcium dialysate and medical parathyroidectomy: case report and literature review. 120
Skin necrosis and protein C deficiency associated with vitamin K depletion in a patient with renal failure. 120
Low-dose tissue plasminogen activator for calciphylaxis. 120
Third-line therapies 120
Painful ulcers in calciphylaxis – combined treatment with maggot therapy and oral pentoxyfillin. 120
Ozonetherapy in a dialyzed patient with calcific uremic arteriolopathy. 120
Intensive tandem cryofiltration apheresis and hemodialysis to treat a patient with severe calciphylaxis, cryoglobulinemia, and end-stage renal disease. 121
36 Capillaritis (pigmented purpuric dermatoses) 122
Management strategy 122
Specific investigations 122
Purpura simplex (inflammatory purpura without vasculitis): a clinicopathologic study of 174 cases. 122
Persistent pigmented purpuric dermatitis: granulomatous variant. 122
Progression of pigmented purpura-like eruptions to mycosis fungoides: report of three cases. 123
CD8-positive mycosis fungoides presenting as capillaritis. 123
Drug-induced chronic pigmented purpura. 123
Drug-induced purpura simplex: clinical and histological characteristics. 123
Acetaminophen-induced progressive pigmentary purpura (Schamberg’s disease). 123
37 Cat scratch disease 125
Management strategy 125
Specific investigations 125
The agent of bacillary angiomatosis. 125
Bartonella-associated infections. 125
Evaluation of sensitivity, specificity and cross-reactivity in Bartonella henselae serology. 125
Cat-scratch disease. 125
Detection by immunofluorescence assay of Bartonella henselae in lymph nodes from patients with cat scratch disease. 125
The use of Bartonella henselae-specific age dependent IgG and IgM in diagnostic models to discriminate diseased from non-diseased in cat scratch disease serology. 126
First-line therapy 126
Bartonellosis. 126
Second-line therapies 126
Prospective randomized double blind placebo-controlled evaluation of azithromycin for treatment of cat-scratch disease. 126
Third-line therapies 126
Immunocompetent individuals 126
Antibiotic therapy for cat-scratch disease: clinical study of therapeutic outcome in 268 patients and a review of the literature. 126
Antimicrobial susceptibility of Rochalimaea quintana, Rochalimaea vinsonii, and the newly recognized Rochalimaea henselae. 126
Hepatosplenic cat-scratch disease in children: selected clinical features and treatment. 126
Successful treatment of cat-scratch disease with ciprofloxacin. 126
Cat-scratch disease of the head and neck in a pediatric population: surgical indications and outcomes. 126
Immunosuppressed individuals 126
Molecular epidemiology of Bartonella infections in patients with bacillary angiomatosis-peliosis. 126
Cat scratch disease, bacillary angiomatosis, and other infections due to Rochalimaea. 126
Cutaneous vascular lesions and disseminated cat-scratch disease in patients with the acquired immunodeficiency syndrome (AIDS) and AIDS-related complex. 126
38 Cellulite 127
Management strategy 127
Specific investigations 127
A validated photonumeric cellulite severity scale. 127
Side-by-side comparison of areas with and without cellulite depressions using magnetic resonance imaging. 127
First-line therapies 127
Subcision: a treatment for cellulite. 127
Treatment of cellulite using a 1440-nm pulsed laser with one-year follow-up. 128
Efficacy of a novel bi-directional sidelight optical fiber & 1440 nm Nd:YAG laser in the treatment of cellulite as measured by 3-dimensional surface imaging. 128
Reduction in thigh circumference and improvement in the appearance of cellulite with dual-wavelength, low-level laser energy and massage. 128
A single center, randomized, comparative, prospective clinical study to determine the efficacy of the VelaSmooth system versus the Triactive system for the treatment of cellulite. 128
Cellulite treatment using a novel combination radiofrequency, infrared light, and mechanical tissue manipulation device. 128
A prospective clinical study to evaluate the efficacy and safety of cellulite treatment using the combination of optical and RF energies for subcutaneous tissue heating. 128
The effectiveness of anticellulite treatment using tripolar radiofrequency monitored by classic and high-frequency ultrasound. 128
A multicenter study of cellulite treatment with a variable emission radio frequency system. 128
Unipolar radiofrequency treatment to improve the appearance of cellulite. 128
Second-line therapies 129
Addition of conjugated linoleic acid to a herbal anticellulite pill. 129
A double-blind evaluation of the activity of an anti-cellulite product containing retinol, caffeine, and ruscogenine by a combination of several non-invasive methods. 129
Topical retinol improves cellulite. 129
Parallel placebo-controlled clinical study of a mixture of herbs sold as a remedy for cellulite. 129
Evaluation of the effects of caffeine in the microcirculation and edema on thighs and buttocks using the orthogonal polarization spectral imaging and clinical parameters. 129
The effectiveness and safety of topical PhotoActif phosphatidylcholine-based anti-cellulite gel and LED (red and near-infrared) light on grade II-III thigh cellulite: a randomized, double-blinded study. 129
Third-line treatments 129
Cellulite treatment: a myth or reality: a prospective randomized, controlled trial of two therapies, endermologie and aminophylline cream. 129
39 Cellulitis and erysipelas 130
Management strategy 130
Specific investigations 130
First-line therapies 130
The course, costs and complications of oral versus intravenous penicillin therapy of erysipelas. 130
Management and morbidity of cellulitis of the leg. 130
Case survey of management of cellulitis in a tertiary teaching hospital. 131
Skin concentrations of phenoxymethylpenicillin in patients with erysipelas. 131
A randomized comparative study of once-daily ceftriaxone and 6-hourly flucloxacillin in the treatment of moderate to severe cellulitis. Clinical efficacy, safety and pharmacoeconomic implications. 131
Roxithromycin versus penicillin in the treatment of erysipelas in adults: a comparative study. 131
Amoxicillin combined with clavulanic acid for the treatment of soft tissue infections in children. 131
Nurse-led management of uncomplicated cellulitis in the community: evaluation of a protocol incorporating intravenous ceftriaxone. 131
Prospective evaluation of the management of moderate to severe cellulitis with parenteral antibiotics at a paediatric day treatment centre. 131
Second-line therapies 131
Ciprofloxacin for soft tissue infections. 131
Teicoplanin in the treatment of skin and soft tissue infections. 131
Twice daily intramuscular imipenem/cilastatin in the treatment of skin and soft tissue infections. 131
Randomized comparison of linezolid (PNU-100766) versus oxacillin-dicloxacillin for treatment of complicated skin and soft tissue infections. 131
Third-line therapies 132
Antibiotic and prednisolone therapy of erysipelas: a randomized, double blind, placebo-controlled study. 132
Randomized placebo controlled trial of granulocyte-colony stimulating factor in diabetic foot infection. 132
Cellulitis owing to Aeromonas hydrophilia: treatment with hyperbaric oxygen. 132
Prophylaxis 132
Prophylactic antibiotics in erysipelas. 132
Cellulitis and erysipelas. 132
Prophylactic antibiotics for the prevention of cellulitis (erysipelas) of the leg: results of the UK Dermatology Clinical Trials Network’s PATCH II trial. 132
40 Chancroid 133
Diagnosis and management strategy 133
Specific investigations 133
First-line therapies 133
European guideline for the management of chancroid, 2011. 133
Treatment of chancroid, 1997. 133
Second-line therapies 133
Sexually transmitted disease treatment guidelines. 133
A randomized, double-blind, placebo-controlled trial of single dose ciprofloxacin versus erythromycin for the treatment of chancroid in Nairobi, Kenya. 134
Third-line therapy 134
Treatment of chancroid, 1997. 134
A comparative study of a single-dose treatment of chancroid using thiamphenicol versus azithromycin. 134
41 Chilblains 135
Management strategy 135
Specific investigations 135
Chilblain lupus erythematosus – a review of literature. 135
Pernio. A possible association with chronic myelomonocytic leukaemia. 135
Anorexia nervosa associated with acromegaloid features, onset of acrocyanosis and Raynaud’s phenomenon and worsening of chilblains. 135
Perniosis in association with anorexia nervosa. 135
Celiac disease presenting with chilblains in an adolescent girl. 135
Childhood pernio and cryoproteins. 135
Equestrian perniosis associated with cold agglutinins: a novel finding. 135
First-line therapies 135
The treatment of chilblains with nifedipine: the results of a pilot study, a double blind placebo-controlled randomized study and a long term open trial. 136
Diltiazem vs. nifedipine in chilblains: a clinical trial. 136
Corticosteroid therapy for pernio. 136
Second-line therapies 136
Chilblains. 136
Third-line therapies 136
Pernio of the hips in young girls wearing tight-fitting jeans with a low waistband. 136
Treatment of perniosis with oral pentoxyfylline in comparison with oral prednisolone plus topical clobetasol ointment in Iraqi patients. 136
Successful treatment of perniosis with hydroxychloroquine. 136
A double blind study of ultraviolet phototherapy in the prophylaxis of chilblains. 136
42 Chondrodermatitis nodularis helicis chronicus 137
Management strategy 137
Specific investigations 137
First-line therapies 137
Treatment of chondrodermatitis nodularis helicis and conventional wisdom? 137
Intralesional triamcinolone for chondrodermatitis nodularis: a follow-up study of 60 patients. 137
Topical nitroglycerin: a promising treatment option for chondrodermatitis nodularis helicis. 137
Second-line therapies 137
The treatment of chondrodermatitis nodularis with cartilage removal alone. 137
Treatment of chondrodermatitis nodularis with removal of the underlying cartilage alone: retrospective analysis of experience in 37 lesions. 138
Twelve years’ experience of simplified surgical treatment of chondrodermatitis nodularis by cartilage trimming and sutureless skin closure. 138
Chondrodermatitis nodularis chronica helicis et antihelices. 138
Narrow elliptical skin excision and cartilage shaving for chondrodermatitis nodularis. 138
Modified surgical excision for the treatment of chondrodermatitis nodularis. 138
Auricular pressure relieving cushions for chondrodermatitis nodularis helicis. 138
Effective treatment of chondrodermatitis nodularis chronica helicis using a conservative approach. 138
Management of chondrodermatitis nodularis chronica helicis using a ‘doughnut pillow’. 138
Management of chondrodermatitis nodularis helicis by auricular pressure-relieving device: a retrospective study. 138
Management of chondrodermatitis helicis by protective padding: a series of 12 cases and a review of the literature. 138
Chondrodermatitis nodularis chronica helicis – a conservative therapeutic approach by decompression. 138
Third-line therapies 139
Chondrodermatitis nodularis chronica helicis treated with curettage and electrocauterization: follow-up of a 15-year material. 139
The surgical management of chondrodermatitis nodularis chronica helicis. 139
Chondrodermatitis nodularis chronica helicis. Successful treatment with the carbon dioxide laser. 139
The punch and graft technique: a novel method of surgical treatment for chondrodermatitis nodularis helicis. 139
43 Chromoblastomycosis 140
Management strategy 140
Specific investigations 140
First-line therapies 141
Treating chromoblastomycosis with systemic antifungals. 141
Chromoblastomycosis. 141
Chromoblastomycosis: an overview of clinical manifestations, diagnosis and treatment. 141
Chromoblastomycosis: clinical and mycologic experience of 51 cases. 141
Subcutaneous mycoses. 141
Pulse itraconazole 400 mg daily in the treatment of chromoblastomycosis. 141
Chromoblastomycosis: a clinical and molecular study of 18 cases in Rio de Janeiro, Brazil. 141
Treatment of chromomycosis with terbinafine: preliminary results of an open pilot study. 141
Treatment of chromoblastomycosis with terbinafine: experience with four cases. 141
Treatment of chromoblastomycosis with terbinafine: a report of four cases. 141
Alternate week and combination itraconazole and terbinafine therapy for chromoblastomycosis caused by Fonsecaea pedrosoi in Brazil. 142
Posaconazole treatment of refractory eumycetoma and chromoblastomycosis. 142
Second-line therapies 142
Treatment of chromoblastomycosis with itraconazole, cryosurgery, and a combination of both. 142
Treatment of chromomycosis by cryosurgery with liquid nitrogen: 15 years’ experience. 142
Successful treatment of chromoblastomycosis with topical heat therapy. 142
Third-line therapies 142
Six years experience in treatment of chromomycosis with 5-fluorocytosine. 142
A case of chromoblastomycosis with an unusual clinical manifestation caused by Phialophora verrucosa on an unexposed area: treatment with a combination of amphotericin B and 5-flucytosine. 142
Extensive chromoblastomycosis caused by Fonsecaea pedrosoi successfully treated with a combination of amphotericin B and itraconazole. 142
Extensive long-standing chromomycosis due to Fonsecaea pedrosoi: three cases with relevant improvement under voriconazole therapy. 143
44 Chronic actinic dermatitis 144
Management strategy 144
Specific investigations 144
The construction and development of a grating monochromator and its application to the study of the reaction of the skin to light. 144
False-negative monochromator phototesting in chronic actinic dermatitis. 144
A case of false-negative monochromator phototesting in a patient with chronic actinic dermatitis taking prednisolone. 144
Chronic actinic dermatitis in the elderly: recognition and treatment. 144
A preliminary investigation into the effect of exposure of photosensitive individuals to light from compact fluorescent lamps. 144
Contact allergic sensitivity to plants and the photosensitivity dermatitis and actinic reticuloid syndrome. 144
Contact and photocontact sensitization in chronic actinic dermatitis: sesquiterpene lactone mix is an important allergen. 144
Contact and photocontact sensitization in chronic actinic dermatitis: a changing picture. 144
Chronic actinic dermatitis in Asian skin: a Singaporean experience. 145
Prevalence and predictors of vitamin D status in patients referred to a tertiary photodiagnostic service: a retrospective study. 145
First-line therapies 145
The quality of life of 790 patients with photodermatoses. 145
Chronic actinic dermatitis: a retrospective analysis of 44 cases referred to an Australian photobiology clinic. 145
Photosensitivity dermatitis/actinic reticuloid syndrome in an Irish population: a review and some unusual features. 145
Protection against ultraviolet radiation by commercial summer clothing: need for standardised testing and labelling. 145
Second-line therapies 145
Azathioprine treatment in chronic actinic dermatitis: a double-blind controlled trial with monitoring of exposure to ultraviolet radiation. 145
Azathioprine in dermatology: a survey of current practice in the UK. 145
Severe chronic actinic dermatitis treated with cyclosporine: 2 cases. 145
Chronic actinic dermatitis treated with mycophenolate mofetil. 145
Chronic actinic dermatitis (photosensitivity dermatitis/actinic reticuloid syndrome): beneficial effect from hydroxyurea. 145
PUVA therapy of chronic actinic dermatitis. 145
Chronic actinic dermatitis: two patients with successful management using narrowband ultraviolet B phototherapy with systemic steroids. 145
Actinic reticuloid. A clinical photobiologic, histopathologic, and follow-up study of 16 patients. 145
Treatment with topical tacrolimus favors chronic actinic dermatitis: a clinical and immunopathological study. 146
Erythrodermic chronic actinic dermatitis responding only to topical tacrolimus. 146
Successful treatment of chronic actinic dermatitis with topical pimecrolimus. 146
Third-line therapies 146
Chronic actinic dermatitis. An analysis of 51 patients evaluated in the United States and Japan. 146
Chronic actinic dermatitis responding to danazol. 146
Recalcitrant chronic actinic dermatitis treated with low-dose thalidomide. 146
Natural α-interferon in chronic actinic dermatitis. Report of a case. 146
Successful therapy of chronic actinic dermatitis with infliximab. 146
45 Coccidioidomycosis 147
Management strategy 147
Specific investigations 147
First-line therapies 147
Fluconazole therapy for coccidioidal meningitis. 147
Fluconazole in the treatment of chronic pulmonary and nonmeningeal disseminated coccidioidomycosis. 148
Itraconazole treatment of coccidioidomycosis. 148
Itraconazole therapy for chronic coccidioidal meningitis. 148
Comparison of oral fluconazole and itraconazole for progressive, nonmeningeal coccidioidomycosis. A randomized, double-blind trial. 148
Second-line therapies 148
Amphotericin B and coccidioidomycosis. 148
Intrathecal amphotericin in the management of coccidioidal meningitis. 148
Use of liposomal amphotericin B in the treatment of disseminated coccidioidomycosis. 148
Ketoconazole therapy of progressive coccidioidomycosis. Comparison of 400- and 800-mg doses and observations at higher doses. 148
Third-line therapies 148
Safety, tolerance, and efficacy of posaconazole therapy in patients with nonmeningeal disseminated or chronic pulmonary coccidioidomycosis. 148
Posaconazole therapy for chronic refractory coccidioidomycosis. 149
Treatment of refractory coccidioidomycosis with voriconazole or posaconazole. 149
Combination therapy of disseminated coccidioidomycosis with caspofungin and fluconazole. 149
Use of the echinocandins (caspofungin) in the treatment of disseminated coccidioidomycosis in a renal transplant recipient. 149
Two cases illustrating successful adjunctive interferon-γ immunotherapy in refractory disseminated coccidioidomycosis. 149
Current guidelines 149
Coccidioidomycosis. Infectious Diseases Society of America Guidelines. 149
Persistent pulmonary infection 149
Diffuse pneumonia 149
Chronic progressive pulmonary infection 149
Disseminated extrapulmonary infection 149
Meningitis 149
46 Condyloma Acuminata 150
Management strategy 150
Specific investigations 150
Evaluation of human papillomavirus testing in primary screening for cervical abnormalities: comparison of sensitivity, specificity, and frequency of referral. 150
Evidence-based treatment and prevention of external genital warts in female pediatric and adolescent patients. 150
First-line therapies 151
Imiquimod, a patient-applied immune response modifier for treatment of external genital warts. 151
Imiquimod 3.75% cream applied daily to treat anogenital warts: combined results from women in two randomized, placebo-controlled studies. 151
Human papillomavirus (HPV) viral load and HPV type in the clinical outcome of HIV-positive patients treated with imiquimod for anogenital warts and anal intraepithelial neoplasia. 151
A multicentre, randomised, double-blind, placebo controlled study of cryotherapy versus cryotherapy and podophyllotoxin cream as treatment for external anogenital warts. 151
Safety and efficacy of 0.5% podofilox gel in the treatment of anogenital warts. 151
Efficacy, safety and tolerability of green tea catechins in the treatment of external anogenital warts: a systematic review and meta-analysis. 151
Treatment of external genital warts: a randomized clinical trial comparing podophyllin, cryotherapy, and electrodesiccation. 151
Second-line therapies 151
Comparison of podophyllin application with simple surgical excision in clearance and recurrence of perianal condyloma acuminata. 151
Human papilloma virus type and recurrence rate after surgical clearance of anal condylomata acuminata. 151
Study of persistence and recurrence rates in 106 patients with condyloma and intraepithelial neoplasia after CO2 laser treatment. 152
Treatment of genital warts in males by pulsed dye laser. 152
Treating vaginal and external anogenital condylomas with electrosurgery vs. CO2 laser ablation. 152
Treatment of external genital warts comparing cryotherapy and trichloroacetic acid. 152
Third-line therapies 152
Natural interferon alfa for treatment of condyloma acuminata. 152
Treatment of condylomata acuminata with oral isotretinoin. 152
Topical cidofovir (HPMPC) is an effective adjuvant to surgical treatment of anogenital condylomata acuminata. 152
Combined surgery and cidofovir is an effective treatment for genital warts in HIV-infected patients. 152
Evaluation of photodynamic therapy using topical aminolevulinic acid hydrochloride in the treatment of condylomata acuminata: a comparative, randomized clinical trial. 152
47 Cryptococcosis 153
Management strategy 153
Specific investigations 153
Cryptococcal disease and HIV infection. 153
First-line therapies 153
Treatment of cryptococcosis in the setting of HIV coinfection. 153
Epidemiology and management of cryptococcal meningitis: developments and challenges. 154
Cryptococcosis in human immunodeficiency virus- negative patients in the era of effective azole therapy. 154
Clinical and epidemiological features of 123 cases of cryptococcosis in Mato Grosso do Sul, Brazil. 154
Combination antifungal therapies for HIV-associated cryptococcal meningitis: a randomised trial. 154
Primary cutaneous cryptococcosis in Brazil: report of 11 cases in immunocompetent and immunosuppressed patients. 154
Cutaneous cryptococcosis in solid organ transplant recipients. 154
Successful use of amphotericin B lipid complex in the treatment of cryptococcosis. 154
High-dose amphotericin B with flucytosine for the treatment of cryptococcal meningitis in HIV-infected patients: a randomized trial. 154
Second-line therapies 154
The efficacy of fluconazole 600 mg/day versus itraconazole 600 mg/day as consolidation therapy of cryptococcal meningitis in AIDS patients. 154
Voriconazole treatment for less-common, emerging, or refractory fungal infections. 154
Third-line therapies 155
Recombinant interferon-gamma 1b as adjunctive therapy for AIDS-related acute cryptococcal meningitis. 155
Guidelines 155
Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the Infectious Diseases Society of America. 155
48 Cutaneous candidiasis and chronic mucocutaneous candidiasis 156
Cutaneous candidiasis 156
Management strategy 156
Specific investigations 156
Diagnosis of superficial mycoses by direct microscopy: a statistical evaluation. 156
First-line therapies 156
A multicenter, open-label study to assess the safety and efficacy of ciclopirox topical suspension 0.77% in the treatment of diaper dermatitis due to Candida albicans. 156
Topical treatment of dermatophytosis and cutaneous candidiasis with flutrimazole 1% cream: double-blind randomized comparative trial with ketoconazole 2% cream. 156
Naftifine cream in the treatment of cutaneous candidiasis. 157
A comparison of nystatin cream with nystatin/triamcinolone acetonide combination cream in the treatment of candidal inflammation of the flexures. 157
Second-line therapies 157
Prospective aetiological study of diaper dermatitis in the elderly. 157
Fluconazole versus ketoconazole in the treatment of dermatophytoses and cutaneous candidiasis. 157
A comparison of the efficacy of oral fluconazole, 150 mg/week versus 50 mg/day, in the treatment of tinea corporis, tinea cruris, tinea pedis, and cutaneous candidosis. 157
Third-line therapies 157
Antifungal activity of Lavandula angustifolia essential oil against Candida albicans yeast and mycelial form. 157
Perianal candidosis: a comparative study with mupirocin and nystatin. 157
Chronic mucocutaneous candidiasis 157
Management strategy 158
Special investigations 158
Chronic mucocutaneous candidiasis in APECED or thymoma patients correlates with autoimmunity to Th17-associated cytokines. 158
STAT1 mutations in autosomal dominant chronic mucocutaneous candidiasis. 158
First-line therapies 158
Long-term therapy of chronic mucocutaneous candidiasis with ketoconazole: experience with twenty-one patients. 158
Itraconazole in the treatment of two young brothers with chronic mucocutaneous candidiasis. 158
Fluconazole in the management of patients with chronic mucocutaneous candidiasis. 158
Voriconazole: a broad spectrum triazole for the treatment of serious and invasive fungal infections. 158
Successful treatment of chronic mucocutaneous candidiasis caused by azole-resistant Candida albicans with posaconazole. 158
Second-line therapies 159
Activity of amphotericin B, anidulafungin, caspofungin, micafungin, posaconazole, and voriconazole against Candida albicans with decreased susceptibility to fluconazole from APECED patients on long-term azole treatment of chronic mucocutaneous candidiasis. 159
Successful treatment of azole-resistant chronic mucocutaneous candidiasis with caspofungin. 159
Prolonged oral treatment of chronic mucocutaneous candidiasis with amphotericin B. 159
Chronic mucocutaneous candidiasis treated with amphotericin B. Case report. 159
Third-line therapies 159
Case report: successful treatment with cimetidine and zinc sulphate in chronic mucocutaneous candidiasis. 159
Transfer factor in chronic mucocutaneous candidiasis. 159
49 Cutaneous larva migrans 160
Management strategy 160
Specific investigations 160
First-line therapies 160
One-week therapy with oral albendazole in hookworm-related cutaneous larva migrans: a retrospective study on 78 patients. 160
Cutaneous larva migrans: clinical features and management of 44 cases presenting in the returning traveler. 160
A randomized trial of ivermectin versus albendazole for the treatment of cutaneous larva migrans. 160
Cutaneous larva migrans in travelers: a prospective study, with assessment of therapy with ivermectin. 160
Treatment of cutaneous larva migrans. 160
Treatment of 18 children with scabies or cutaneous larva migrans using ivermectin. 160
Second-line therapies 161
Efficacy and tolerability of thiabendazole in a lipophil vehicle for cutaneous larva migrans. 161
Third-line therapies 161
Efficacy of albendazole ointment on cutaneous larva migrans in 2 young children. 161
Epidemiological and clinical characteristics of hookworm-related cutaneous larva migrans. 161
50 Cutaneous polyarteritis nodosa 162
Management strategy 162
Specific investigations 162
Cutaneous periarteritis nodosa: a clinicopathological study of 79 cases. 162
A case of cutaneous polyarteritis nodosa associated with ulcerative colitis. 162
High titer of phosphatadylserine–prothrombin complex antibodies in patients with cutaneous polyarteritis nodosa. 162
Hepatitis C virus infection in cutaneous polyarteritis nodosa: a retrospective study of 16 cases. 162
Polyarteritis-like vasculitis in association with minocycline use: a single center case series. 163
First-line therapies 163
Low-dose weekly methotrexate for unusual neutrophilic vascular reactions: cutaneous polyarteritis nodosa and Behçet’s disease. 163
Use of mizoribine in two patients with recalcitrant cutaneous polyarteritis nodosa. 163
Ulcerative cutaneous polyarteritis nodosa treated with mycophenolate mofetil and pentoxifylline. 163
Second-line therapies 163
Intravenous immunoglobulins as treatment of severe cutaneous polyarteritis nodosa. 163
Successful treatment of cutaneous PAN with pentoxifylline. 163
Third-line therapies 163
Estrogen-sensitive cutaneous polyarteritis nodosa: response to tamoxifen. 163
Successful response to infliximab in a patient with undifferentiated spondyloarthropathy coexisting with polyarteritis nodosa-like cutaneous vasculitis. 163
Successful treatment of childhood cutaneous polyarteritis nodosa with infliximab. 163
Cutaneous polyarteritis nodosa: therapy and clinical course in four cases. 163
Use of warfarin therapy at a target international normalized ratio of 3.0 for cutaneous polyarteritis nodosa. 163
51 Darier disease 164
Management strategy 164
Investigations 164
Darier-White disease: a review of the clinical features in 163 patients. 164
First-line therapies 164
Darier’s disease. 164
Linear Darier’s disease successfully treated with 0.1% tazarotene gel ‘short contact’ therapy. 164
Topical isotretinoin in Darier’s disease. 164
Successful treatment of Darier’s disease with adapalene gel. 164
Second-line therapies 164
Clinical and ultrastructural effects of acitretin in Darier’s disease. 164
Isotretinoin treatment of Darier’s disease. 165
Etretinate may work where acitretin fails. 165
Successful treatment of Darier disease with oral alitretinoin. 165
Efficacy and safety of oral retinoids in different psoriasis subtypes: a systematic literature review. 165
Efficacy and risks of topical 5-fluorouracil in Darier’s disease. 165
A case of Darier’s disease successfully treated with topical tacrolimus. 165
Third-line therapies 165
Darier’s disease: severe eczematization successfully treated with cyclosporine. 165
Vulval Darier’s disease treated successfully with cyclosporine. 165
Vesiculobullous Darier’s disease responsive to oral prednisolone. 165
Extensive recalcitrant Darier disease successfully treated with laser ablation. 165
Efficacy of erbium:YAG laser ablation in Darier disease and Hailey-Hailey disease. 165
Successful treatment of Darier disease with the flashlamp-pumped pulse-dye laser. 165
Treatment of Darier’s disease with photodynamic therapy. 165
Botulinum toxin type A: an alternative symptomatic management of Darier’s disease. 165
Treatment of recalcitrant Darier’s disease with electron beam therapy. 165
Electrosurgical treatment of etretinate-resistant Darier’s disease. 165
Dermabrasion in Darier’s disease. 165
The surgical treatment of hypertrophic Darier’s disease. 166
The surgical treatment of hypertrophic intertriginous Darier’s disease. 166
An effective surgical treatment for nail thickening in Darier’s disease. 166
52 Decubitus ulcers 167
Management strategy 167
Prevention 167
Management 167
Removal of necrotic debris 167
Maintenance of a moist wound environment 167
Correction of the underlying contributing factors 168
General measures 168
Blanchable erythema and non-blanchable erythema 168
Decubitus dermatitis 168
Superficial and deep ulcers 168
Underlying contributing factors 168
Specific investigations 168
Categories of patient 168
Grading or evaluation 169
Dermatologic observation 169
Staging 169
Pressure sores among hospitalized patients. 169
Anaemia and serum protein alteration in patients with pressure ulcers. 169
Characteristics of hospitalised US veterans with nosocomial pressure ulcers. 169
Risk factors associated with pressure ulcer development in critically ill traumatic spinal cord injury patients. 169
Pathophysiology of acute wound healing. 169
Pressure ulcer tissue histology: an appraisal of current knowledge. 169
A review of scales for assessing the risk of developing a pressure ulcer in individuals with SCI. 169
25 years of pressure ulcers. 169
Pressure ulcer staging revisited: superficial skin changes and deep pressure ulcer framework. 169
National Pressure Ulcer Advisory Panel. Pressure ulcers: avoidable or unavoidable? Results of the national pressure ulcer advisory panel consensus conference. 169
Enhancing Braden pressure ulcer risk assessment in acutely ill adult veterans. 169
First-line therapies 169
Eliminating pressure and relieving devices 170
An investigation of geriatric nursing problems in hospital. 170
Shearing force as a factor in decubitus ulcers in paraplegics. 170
Drawsheets for prevention of decubitus ulcer. 170
Decubitus prophylaxis: a prospective trial on the efficiency of alternating-pressure air mattresses and water mattresses. 170
The effectiveness of preventive management in reducing the occurrence of pressure sores. 170
Influence of 30 degrees laterally inclined position and the supersoft 3-piece mattress on areas of maximum pressure and implications for pressure sore prevention. 170
Mechanical loading and support surfaces. 170
A clinical comparison of two pressure reducing surfaces in the management of pressure ulcers. 170
A randomized trial of low-air-loss beds for treatment of pressure ulcers. 170
Comparison of total body tissue interface pressure of specialized pressure-relieving mattresses. 170
Lateral rotation mattresses for wound healing. 170
Dilemmas about the decubitus ulcer: skin-fold ulcerations and apposition lesions. 170
Support surfaces for treating pressure ulcers. 170
Debridement 170
Collagenase in the treatment of dermal and decubitus ulcers. 170
The care of decubitus ulcers, pressure ulcers. 170
Cleansing the traumatic wound by high pressure syringe irrigation. 170
Dissolution of wound coagulum and promotion of granulation tissue under DuoDERM. 170
Debridement of cutaneous ulcer: medical and surgical aspects. 170
Pressure ulcer treatment guide: quick reference guide for clinicians No. 15. 170
Maggot debridement therapy of infected ulcers: patient and wound factors influencing outcome – a study of 101 patients with 117 wounds. 170
The role of surgical debridement in healing of diabetic foot ulcers. 171
Antimicrobial agents 171
Relationship of quantitative wound bacterial counts to healing of decubiti: effect of topical gentamicin. 171
Topical metronidazole gel: the bacteriology of decubitus ulcers. 171
Does this patient have an infection of a chronic wound? 171
Nutrition 171
Ascorbic acid supplementation in the treatment of pressure sores. 171
The importance of dietary protein in healing pressure ulcers. 171
Nutritional interventions for preventing and treating pressure ulcers. 171
Old age, malnutrition, and pressure sores: an ill-fated alliance. 171
Second-line therapies 171
A comparison of the efficacy and cost-effectiveness of two methods of managing pressure ulcers. 171
Advances in wound healing. 171
Third-line therapies 171
Hyperbaric oxygen therapy for chronic wounds. 171
Clinical aspects of full-thickness wound healing. 171
53 Delusions of parasitosis 172
Management strategy 172
Specific investigations 173
Clinical, epidemiologic, histopathologic and molecular features of an unexplained dermopathy. 173
Delusions of parasitosis. A dermatologist’s guide to diagnosis and treatment. 173
Delusions of parasitosis. 173
One hundred years of delusional parasitosis. Meta-analysis of 1223 case reports. 173
Diffuse pruritic lesions in a 37-year-old man after sleeping in an abandoned building. 173
First-line therapies 174
Pimozide in dermatologic practice: a comprehensive review. 174
Delusional parasitosis: a dermatologic, psychiatric, and pharmacologic approach. 174
Neurotropic and psychotropic drugs in dermatology. 174
Delusions of parasitosis. A psychiatric disorder to be treated by dermatologists? An analysis of 33 patients. 174
Second-line therapies 174
Second-generation antipsychotics in primary and secondary delusional parasitosis: outcome and efficacy. 174
Therapeutic update: use of risperidone for the treatment of monosymptomatic hypochondriacal psychosis. 174
Primary delusional parasitosis treated with olanzapine. 174
Aripiprazole as a viable alternative for treating delusions of parasitosis. 174
Promazine in the treatment of delusional parasitosis. 174
Atypical antipsychotics in the treatment of delusional parasitosis. 174
Antipsychotic treatment of primary delusional parasitosis: systematic review. 174
54 Dermatitis artefacta 175
Management strategy 175
Specific investigations 175
Self-induced skin lesions: a review of dermatitis artefacta. 175
Cutaneous manifestations of psychiatric disease that commonly present to the dermatologist – diagnosis and treatment. 175
Dermatitis artefacta: a review of 14 cases. 176
Dermatitis artefacta in pediatric patients: experience at the National Institute of Pediatrics. 176
Dermatitis artefacta in a child. 176
First-line therapies 176
Diagnostic clues to dermatitis artefacta. 176
Self-inflicted skin diseases. A retrospective analysis of 57 patients with dermatitis artefacta seen in a dermatology department. 176
Training future dermatologists in psychodermatology. 176
Dermatitis artefacta. Clinical features and approach to treatment. 176
The current management of delusional parasitosis and dermatitis artefacta. 176
Second-line therapies 176
Treatment of self-mutilation with olanzapine. 176
Olanzapine is effective in the management of some self-induced dermatoses: case reports. 176
55 Dermatitis herpetiformis 177
Management strategy 177
Specific investigations 177
Deposition of granular IgA relative to clinical lesions in dermatitis herpetiformis. 177
Dermatitis herpetiformis: from the genetics to the development of skin lesions. 178
First-line therapies 178
Suggested guidelines for patient monitoring: hepatic and hematologic toxicity attributable to systemic dermatologic drugs. 178
Advances in celiac disease and gluten free diet. 178
A long-term gluten-free diet as an alternative treatment in severe forms of dermatitis herpetiformis. 178
Second-line therapies 178
Management of dermatitis herpetiformis. 178
The effect of elemental diet with and without gluten on disease activity in dermatitis herpetiformis. 178
Third-line therapies 178
Dermatitis herpetiformis effectively treated with heparin, tetracycline and nicotinamide. 178
A rare case of dermatitis herpetiformis requiring parenteral heparin for long-term control. 178
Efficacy of cyclosporine in two patients with dermatitis herpetiformis resistant to conventional therapy. 178
Dermatitis herpetiformis responsive to systemic corticosteroids. 179
Treatment of dermatitis herpetiformis with colchicine. 179
56 Dermatofibrosarcoma protuberans 180
Management strategy 180
Specific investigations 180
Dermatofibrosarcoma protuberans is a unique fibrohistiocytic tumour expressing CD34. 180
Stromelysin-3 (ST3) expression in the differential diagnosis of dermatofibroma (DF) and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34. 180
Differential expression of HMGA1 and HMGA2 in dermatofibroma and dermatofibrosarcoma protuberans: potential diagnostic applications, and comparison with histologic findings, CD34, and factor XIIIa immunoreactivity. 181
First-line therapies 181
Dermatofibrosarcoma protuberans: a report on 29 patients treated by Mohs micrographic surgery (MMS) with long-term follow-up and review of the literature. 181
Dermatofibrosarcoma protuberans: wide local excision vs. Mohs micrographic surgery. 181
Outcomes in 11 patients with dermatofibrosarcoma protuberans treated with Mohs micrographic surgery. 181
Dermatofibrosarcoma protuberans: 35 patients treated with Mohs micrographic surgery using paraffin sections. 181
Surgical treatment of dermatofibrosarcoma protuberans using wide local excision combined with Mohs micrographic surgery. 181
Second-line therapies 181
Treatment of advanced dermatofibrosarcoma protuberans with imatinib mesylate with or without surgical resection. 181
Advanced dermatofibrosarcoma protuberans treated with imatinib mesylate. 181
Using imatinib as neoadjuvant therapy in dermatofibrosarcoma protuberans: potential pluses and minuses. 181
Imatinib mesylate as a preoperative therapy in dermatofibrosarcoma: results of a multicenter phase II study on 25 patients. 181
Radiation in management of patients with dermatofibrosarcoma protuberans. 182
Dermatofibrosarcoma protuberans: treatment results of 35 cases. 182
57 Dermatomyositis 183
Management strategy 183
Specific investigations 183
Scalp involvement in dermatomyositis. Often overlooked or misdiagnosed. 183
Influence of age on characteristics of polymyositis and dermatomyositis in adults. 183
MR imaging in amyopathic dermatomyositis. 183
The value of malignancy evaluation in patients with dermatomyositis. 184
Frequency of specific cancer types in dermatomyositis and polymyositis: a population-based study. 184
A new approach to the classification of idiopathic inflammatory myopathy: myositis-specific autoantibodies define useful homogeneous patient groups. 184
Clinical correlations with dermatomyositis-specific autoantibodies in adult Japanese patients with dermatomyositis: a multicenter cross-sectional study. 184
Insterstitial lung disease in classic and skin-predominant dermatomyositis: a retrospective study with screening recommendations. 184
Incidence of dermatomyositis and clinically amyopathic dermatomyositis: a population-based study in Olmstead County, Minnesota. 184
First-line therapies 184
The use of pulse corticosteroid therapy for juvenile dermatomyositis. 185
Dermatomyositis: comparative studies of cutaneous photosensitivity in lupus erythematosus and normal subjects. 185
Cutaneous lesions of dermatomyositis are improved by hydroxychloroquine. 185
Combination antimalarials in the treatment of cutaneous dermatomyositis: a retrospective study. 185
Second-line therapies 185
Topical tacrolimus 0.1% ointment for refractory skin disease in dermatomyositis: a pilot study. 185
Low-dose methotrexate administered weekly is an effective corticosteroid-sparing agent for the treatment of the cutaneous manifestations of dermatomyositis. 185
Mycophenolate mofetil as an effective corticosteroid-sparing therapy for recalcitrant dermatomyositis. 185
Mycophenolate mofetil in dermatomyositis: is it safe? 185
A controlled trial of high-dose intravenous immune globulin infusions as treatment for dermatomyositis. 185
Chlorambucil. An effective corticosteroid-sparing agent for patients with recalcitrant dermatomyositis. 186
Cyclosporine A and intravenous immunoglobulin treatment in polymyositis/dermatomyositis. 186
Cyclosporine A versus methotrexate in the treatment of polymyositis and dermatomyositis. 186
Rituximab in the treatment of dermatomyositis: an open-label pilot study. 186
A pilot trial of rituximab in the treatment of patients with dermatomyositis. 186
Rituximab in the treatment of refractory adult and juvenile dermatomyositis (DM) and adult polymyositis (PM): a randomized, placebo-phase trial. (The RIM Study). 186
Third-line therapies 186
Regression of calcinosis during diltiazem treatment in juvenile dermatomyositis. 186
Calcinosis cutis occurring in association with autoimmune connective tissue disease: the Mayo Clinic experience with 78 patients, 1996–2009. 186
Response to total body irradiation in dermatomyositis. 186
Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate. 187
A randomized, pilot trial of etanercept in dermatomyositis. 187
Improvement in dermatomyositis rash associated with the use of antiestrogen medication. 187
Rapamycin (sirolimus) as a steroid-sparing agent in dermatomyositis. 187
Efficacy of allogeneic mesenchymal stem cell transplantation in patients with drug-resistant polymyositis and dermatomyositis. 187
58 Diaper dermatitis 188
Management strategy 188
Specific investigations 188
Amoxicillin and diaper dermatitis. 188
The role of allergic contact dermatitis in diaper dermatitis. 188
Diaper dermatitis: a review and update. 188
First-line therapy 188
Prevention, diagnosis, and management of diaper dermatitis. 189
Diaper dermatitis and advances in diaper technology. 189
Second-line therapy 189
Efficacy and safety of two different antifungal pastes in infants with diaper dermatitis: a randomized, controlled study. 189
Absorption and efficacy of miconazole nitrate 0.25% ointment in infants with diaper dermatitis. 189
Topical miconazole nitrate ointment in the treatment of diaper dermatitis complicated by candidiasis. 189
Pediatricians who prescribe clotrimazole-betamethasone dipropionate (Lotrisone) often utilize it in inappropriate settings regardless of their knowledge of the drug’s potency. 189
Third-line therapy 189
Skin benefits from continuous topical administration of a zinc oxide/petrolatum formulation by a novel disposable diaper. 189
Contact dermatitis. 189
59 Discoid eczema 190
Management strategy 190
Specific investigations 190
Pityriasis rosea and discoid eczema: dose related reactions to treatment with gold. 190
Severe, generalized nummular eczema secondary to interferon alpha-2b plus ribavirin combination therapy in a patient with chronic hepatitis C virus infection. 190
Cutaneous disease and alcohol misuse. 190
Patch testing in discoid eczema. 190
Patch testing in discoid eczema. 191
Challenge with metal salts. (II). Various types of eczema. 191
Dental infection associated with nummular eczema as an overlooked focal infection. 191
First-line therapies 191
Successful treatment of therapy-resistant atopic dermatitis with clobetasol propionate and a hydrocolloid occlusive dressing. 191
Nummular eczema. A review, follow-up and analysis of a series of 325 cases. 191
The antipruritic effect of 5% doxepin cream in patients with eczematous dermatitis. 191
Second-line therapies 191
Photochemotherapy beyond psoriasis. 191
Half-side comparison study on the efficacy of 8-methoxypsoralen bath–PUVA versus narrow-band ultraviolet B phototherapy in patients with severe chronic atopic dermatitis. 191
Antimicrobial effects of phototherapy and photochemotherapy in vivo and in vitro. 191
Suppressive effect of ultraviolet (UVB and PUVA) radiation on superantigen production by Staphylococcus aureus. 191
Hand dermatitis: a review of clinical features, therapeutic options, and long-term outcomes. 191
Long-term efficacy and safety of cyclosporine in severe adult atopic dermatitis. 192
Third-line therapies 192
Azathioprine in dermatological practice. An overview with special emphasis on its use in non-bullous inflammatory dermatoses. 192
Azathioprine in dermatology: a survey of current practice in the UK. 192
Methotrexate is a safe and effective treatment for paediatric discoid (nummular) eczema: a case series of 25 children. 192
Hypnosis in dermatology. 192
60 Discoid lupus erythematosus 193
Management strategy 193
Specific investigations 193
Cutaneous lupus erythematosus: issues in diagnosis and treatment. 193
First-line therapies 193
Photoprovocation in cutaneous lupus erythematosus: a multicenter study evaluating a standardized protocol. 193
Photoprotective effects of a broad-spectrum sunscreen in ultraviolet-induced cutaneous lupus erythematosus: a randomized, vehicle-controlled, double-blind study. 193
Efficacy of tacrolimus 0.1% ointment in cutaneous lupus erythematosus: a multicenter, randomized, double-blind, vehicle controlled trial. 193
Effectiveness of topical calcineurin inhibitors as monotherapy or in combination with hydroxychloroquine in cutaneous lupus erythematosus. 194
Second-line therapies 194
Clinical and pharmacogenetic influences on response to hydroxychloroquine in discoid lupus erythematosus: a retrospective cohort study. 194
Impact of smoking in cutaneous lupus erythematosus. 194
Low blood concentrations of hydroxychloroquine in patients with refractory cutaneous lupus erythematosus: a French multicenter prospective study. 194
Hypertrophic lupus erythematosus treated successfully with acitretin as monotherapy. 194
Third-line therapies 194
Drugs for discoid lupus erythematosus. 194
Cutaneous lupus erythematosus: update of therapeutic options. Parts I and II. 194
61 Dissecting cellulitis of the scalp 195
Management strategy 195
Specific investigations 195
Tinea capitis mimicking dissecting cellulitis: a distinct variant. 195
Inflammatory tinea capitis (kerion) mimicking dissecting cellulitis. 195
Dissecting cellulitis of the scalp in 2 girls. 195
Squamous cell carcinoma arising in dissecting perifolliculitis of the scalp. 195
Folliculotropic mycosis fungoides with large cell transformation presenting as dissecting cellulitis of the scalp. 195
First-line therapies 195
Management of primary cicatricial alopecias: options for treatment. 195
Perifolliculitis capitis abscedens et suffodiens. 195
Perifolliculitis capitis abscedens et suffodiens (dissecting cellulitis of the scalp). 196
Dissecting cellulitis of the scalp responding to oral quinolones. 196
Second-line therapies 196
Dissecting cellulitis of the scalp: response to isotretinoin. 196
Perifolliculitis capitis: successful control with alternate day corticosteroids. 196
Third-line therapies 196
Dissecting cellulitis of the scalp. 196
Dissecting cellulitis treated with the long-pulsed Nd:YAG laser. 196
Use of an 800-nm pulsed-diode laser in the treatment of recalcitrant dissecting cellulitis of the scalp. 196
Treatment of perifolliculitis capitis abscedens et suffodiens with carbon dioxide laser. 196
Modern external beam radiation therapy for refractory dissecting cellulitis of the scalp. 196
Successful treatment of dissecting cellulitis and acne conglobata with oral zinc. 196
Perifolliculitis capitis abscedens et suffodiens successfully controlled with topical isotretinoin. 196
Perifolliculitis capitis abscedens et suffodiens successfully controlled with infliximab. 196
Three cases of dissecting cellulitis of the scalp treated with adalimumab. 196
62 Drug eruptions 197
Management strategy 197
Specific investigations 197
Genetic predisposition of life-threatening antiepileptic-induced skin reactions. 197
Skin testing in delayed reactions to drugs. 197
Drug provocation tests in hypersensitivity drug reactions. 197
Allergy diagnostic testing: an updated practice parameter. 197
First-line therapies 198
Guidelines of care for cutaneous adverse drug reactions. 198
Second-Line therapies 198
Prophylaxis and treatment of dermatologic adverse events from epidermal growth factor receptor inhibitors. 198
Anticonvulsant hypersensitivity syndrome treated with intravenous immunoglobulin. 198
Open trial of cyclosporine treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis. 198
Effects of treatments on the mortality of Stevens–Johnson syndrome and toxic epidermal necrolysis: a retrospective study on patients included in the prospective EuroSCAR study. 198
Erythema multiforme, Stevens–Johnson syndrome, and toxic epidermal necrolysis: acute ocular manifestations, causes and management. 198
Other therapies 198
Anticonvulsant hypersensitivity syndrome: an update. 198
General considerations on rapid desensitization for drug hypersensitivity: a consensus statement. 199
63 Eosinophilic fasciitis 200
Management strategy 200
Specific investigations 200
Eosinophilic fasciitis. 200
Serum aldolase level is a useful indicator of disease activity in eosinophilic fasciitis. 200
From diagnosis to remission: place of MRI in eosinophilic fasciitis. 200
Eosinophilic fasciitis: spectrum of MRI findings. 201
Eosinophilic fasciitis associated with tryptophan ingestion: a manifestation of eosinophilia myalgia syndrome. 201
Eosinophilic fasciitis associated with Mycoplasma arginini infection. 201
Eosinophilic fasciitis. A pathologic study of twenty cases. 201
First-line therapies 201
Eosinophilic fasciitis: clinical spectrum and therapeutic response in 52 cases. 201
Eosinophilic fasciitis (Shulman disease): new insights into the therapeutic management from a series of 34 patients. 201
Two cases of eosinophilic fasciitis. 201
Eosinophilic fasciitis associated with autoimmune thyroid disease and myelodysplasia treated with pulsed methylprednisolone and antihistamines. 201
Second-line therapies 201
Eosinophilic rheumatic disorders. 201
Eosinophilic fasciitis following exposure to trichloroethylene: successful treatment with cyclosporine. 201
Eosinophilic fasciitis successfully treated with cyclosporine. 201
Long-term remission by cyclosporine in a patient with eosinophilic fasciitis associated with primary biliary cirrhosis. 202
Treatment of eosinophilic fasciitis with methotrexate. 202
The fasciitis–panniculitis syndromes. Clinical and pathologic features. 202
The fasciitis–panniculitis syndrome: clinical spectrum and response to cimetidine. 202
Eosinophilic fasciitis responsive to cimetidine. 202
Third-line therapies 202
Eosinophilic fasciitis treated with psoralen–ultraviolet A bath photochemotherapy. 202
Extracorporeal photochemotherapy in the treatment of eosinophilic fasciitis. 202
D-Penicillamine in the treatment of eosinophilic fasciitis: case reports and review of the literature. 202
Eosinophilic fasciitis with late onset arthritis responsive to sulfasalazine. 202
Surgical management of eosinophilic fasciitis of the upper extremity. 202
Use of infliximab, an anti-tumor necrosis alpha antibody, for inflammatory dermatoses. 202
Infliximab effective in steroid-dependent juvenile eosinophilic fasciitis. 202
Infliximab may be effective in the treatment of steroid-resistant eosinophilic fasciitis: report of three cases. 202
Eosinophilic fasciitis successfully treated with oral hydroxyzine: a new therapeutic use of an old drug? 203
Rituximab in refractory autoimmune diseases: Brazilian experience with 29 patients (2002–2004). 203
Dapsone treatment for eosinophilic fasciitis. 203
Eosinophilic fasciitis and combined UVA1-retinoid-corticosteroid treatment: two case reports. 203
Eosinophilic fasciitis in a pediatric patient. 203
64 Epidermal nevi 204
Management strategy 204
Specific investigations 204
Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis. 204
Squamous cell carcinoma arising in a verrucous epidermal naevus. 204
Basal cell carcinoma developing in verrucous epidermal nevus. 204
Epidermal nevus syndromes. 205
Epidermal nevus syndromes: clinical findings in 35 patients. 205
Does inflammatory linear verrucous epidermal nevus represent a segmental type 1/type 2 mosaic of psoriasis? 205
Verrucous epidermal nevi 205
First-line therapies 205
Comparison of treatment modalities for epidermal nevus: a case report and review. 205
Epidermal nevus: surgical treatment by partial-thickness skin excision. 205
Assessment of cryotherapy for the treatment of verrucous epidermal nevi. 205
Second-line therapies 205
Epidermal nevi treated by carbon dioxide laser vaporization: a series of 25 patients. 205
Laser therapy of verrucous epidermal naevi. 205
Er : YAG laser treatment of verrucous epidermal nevi. 205
Successful treatment of dark-coloured epidermal nevus with ruby laser. 205
Third-line therapies 205
A case of verrucous epidermal naevus successfully treated with acitretin. 206
Topical tretinoin and 5-fluorouracil in the treatment of linear verrucous epidermal nevus. 206
Verrucous epidermal nevus successfully treated with photodynamic therapy. 206
Inflammatory/dysplastic epidermal nevi 206
First-line therapies 206
Successful treatment of inflammatory linear verrucous epidermal nevus with tacrolimus and fluocinonide. 206
Second-line therapies 206
Topical calcipotriol for the treatment of inflammatory linear verrucous epidermal nevus. 206
Successful therapy of an ILVEN in a 7-year-old girl with calcipotriol. 206
Acitretin treatment of a systematized inflammatory linear verrucous epidermal naevus. 206
Dithranol in the treatment of inflammatory linear verrucous epidermal nevus. 206
Third-line therapies 206
Pulsed dye laser for inflammatory linear verrucous epidermal nevus. 206
Carbon dioxide laser therapy for an inflammatory linear verrucous epidermal nevus: a case report. 206
Full-thickness surgical excision for the treatment of inflammatory linear verrucous epidermal nevus. 207
Successful treatment of a widespread inflammatory verrucous epidermal nevus with etanercept. 207
Inflammatory linear verrucous epidermal nevus successfully treated with methyl-aminolevulinate photodynamic therapy. 207
65 Epidermodysplasia verruciformis 208
Management strategy 208
Specific investigations 208
Human papillomavirus-associated tumors of the skin and mucosa. 208
Common variable immunodeficiency syndrome associated with epidermodysplasia verruciformis. 208
Epidermodysplasia verruciformis in the setting of graft-versus-host disease. 208
Generalized verrucosis: a review of the associated diseases, evaluation, and treatments. 208
First-line therapies 208
Second-line therapies 208
Treatment of epidermodysplasia verruciformis with a combination of acitretin and interferon alfa-2a. 209
Systemic low-dose isotretinoin maintains remission status in epidermodysplasia verruciformis. 209
Treatment of a patient with epidermodysplasia verruciformis carrying novel EVER2 mutation with imiquimod. 209
Epidermodysplasia verruciformis, unsuccessful therapeutic approach with imiquimod. 209
Acquired epidermodysplasia verruciformis syndrome in HIV-infected pediatric patients: prospective treatment trial with topical glycolic acid and human papillomavirus genotype characterization. 209
Epidermodysplasia verruciformis in human immunodeficiency virus-infected patients: a marker of human papillomavirus-related disorders not affected by antiretroviral therapy. 209
Third-line therapies 209
Photodynamic therapy for human papillomavirus-related diseases in dermatology. 209
CO2 laser treatment of warts in immunosuppressed patients. 209
Skin autografts in epidermodysplasia verruciformis: human papillomavirus-associated cutaneous changes need over 20 years for malignant conversion. 209
66 Epidermolysis bullosa 210
Management strategy 210
Specific investigations 211
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB. 211
First-line therapies 211
A consensus approach to wound care in epidermolysis bullosa. 211
Management of epidermolysis bullosa in infants and children. 211
The challenges of meeting nutritional requirements in children and adults with epidermolysis bullosa: proceedings of a multidisciplinary team study day. 211
Second-line therapies 211
Tissue-engineered skin (Apligraf) in the healing of patients with epidermolysis bullosa wounds. 211
Apligraf in the treatment of severe mitten deformity associated with recessive dystrophic epidermolysis bullosa. 211
Amniotic membrane grafting in patients with epidermolysis bullosa with chronic wounds. 211
Third-line therapies 211
Bone marrow transplantation for recessive dystrophic epidermolysis bullosa. 212
Punch grafting of chronic ulcers in patients with laminin-332-deficient, non-Herlitz junctional epidermolysis bullosa. 212
Treatment of epidermolysis bullosa simplex with tetracycline. 212
Tetracycline and epidermolysis bullosa simplex: a double-blind, placebo-controlled, crossover randomized clinical trial. 212
The efficacy of trimethoprim in wound healing of patients with epidermolysis bullosa: a feasibility trial. 212
Chemoprevention of squamous cell carcinoma in recessive dystrophic epidermolysis bullosa: results of a phase I trial of systemic isotretinoin. 212
Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. 212
Risk of squamous cell carcinoma in junctional epidermolysis bullosa, non-Herlitz type: report of 7 cases and a review of the literature. 212
67 Epidermolysis bullosa acquisita 213
Management strategy 213
Specific investigations 213
Epidermolysis bullosa acquisita: ultrastructural and immunological studies. 213
Identification of the skin basement-membrane autoantigen in epidermolysis bullosa acquisita. 213
Development of an ELISA for rapid detection of anti-type VII collagen autoantibodies in epidermolysis bullosa acquisita. 213
IgA-mediated epidermolysis bullosa acquisita: two cases and review of the literature. 214
Epidermolysis bullosa acquisita and inflammatory bowel disease. 214
The epidermolysis bullosa acquisita antigen (type VII collagen) is present in human colon and patients with Crohn’s disease have autoantibodies to type VII collagen. 214
Black patients of African descent and HLA-DRB1*15:03 frequency overrepresented in epidermolysis bullosa acquisita. 214
Congenital epidermolysis bullosa acquisita: vertical transfer of maternal autoantibody from mother to infant. 214
First-line therapies 214
Epidermolysis bullosa acquisita – a pemphigoid-like disease. 214
Childhood IgA-mediated epidermolysis bullosa acquisita responding to mycophenolate mofetil as a corticosteroid-sparing agent. 214
Mycophenolate mofetil in epidermolysis bullosa acquisita. 214
Bullous pemphigoid and epidermolysis bullosa acquisita: presentation, prognosis, and immunotherapy in 11 children. 214
Epidermolysis bullosa acquisita responsive to dapsone therapy. 214
Second-line therapies 214
Severe, refractory epidermolysis bullosa acquisita complicated by an oesophageal stricture responding to intravenous immune globulin. 214
Treatment of epidermolysis bullosa acquisita with intravenous immunoglobulin in patients non-responsive to conventional therapy: clinical outcome and post-treatment long-term follow-up. 215
Colchicine for epidermolysis bullosa acquisita. 215
Oral cyclosporine in the treatment of inflammatory and noninflammatory cases. A clinical and immunopathologic analysis. 215
Third-line therapies 215
Successful adjuvant treatment of recalcitrant epidermolysis bullosa acquisita with anti-CD20 antibody rituximab. 215
A successful therapeutic trial of rituximab in the treatment of a patient with recalcitrant, high-titre epidermolysis bullosa acquisita. 215
Epidermolysis bullosa acquisita following bullous pemphigoid, successfully treated with anti-CD20 monoclonal antibody rituximab. 215
Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab. 215
Clinical response of severe mechanobullous epidermolysis bullosa acquisita to combined treatment with immunoadsorption and rituximab (anti-CD20 monoclonal antibodies). 216
Treatment of pemphigus vulgaris with rituximab and intravenous immune globulin. 216
68 Erosive pustular dermatosis 217
Management strategy 217
First-line therapy 217
Chronic atrophic erosive dermatosis of the scalp and extremities: a recharacterization of erosive pustular dermatosis. 217
Erosive pustular dermatosis of the scalp. 217
Second-line therapies 217
Erosive pustular dermatosis of the scalp: a review with a focus on dapsone therapy. 217
Erosive pustular dermatosis of the scalp: treatment with topical tacrolimus. 217
Third-line therapies 217
Disseminated erosive pustular dermatosis also involving the mucosa: successful treatment with oral dapsone. 218
Atypical erosive pustular dermatosis of the scalp with eosinophilia and erythroderma. 218
Erosive pustular dermatosis of the scalp: an uncommon condition typical of elderly patients. 218
Erosive pustular dermatosis of the scalp successfully treated with oral zinc sulphate. 218
Erosive pustular dermatosis of the scalp: a successful treatment with photodynamic therapy. 218
Aminolevulinic acid photodynamic therapy in the treatment of erosive pustular dermatosis of the scalp. 218
Erosive pustular dermatosis of the scalp: a case treated successfully with isotretinoin. 218
Erosive pustular dermatosis of the scalp responding to acitretin. 218
Erosive pustular dermatosis of the scalp successfully treated with calcipotriol cream. 218
69 Erythema annulare centrifugum 219
Management strategy 219
Specific investigations 220
Gyrate erythema. 220
Allergic confirmation that some cases of erythema annulare centrifugum are dermatophytids. 220
Erythema annulare centrifugum and intestinal Candida albicans infection – coincidence or connection? 220
Erythema annulare centrifugum: a review of 24 cases with special reference to its association with underlying disease. 220
Erythema annulare centrifugum: results of a clinicopathologic study of 73 patients. 220
Clinicopathologic analysis of 66 cases of erythema annulare centrifugum. 220
Erythema annular centrifugum in a HIV-positive patient. 220
Erythema annulare centrifugum induced by generalized Phthirus pubis infestation. 220
Erythema annulare centrifugum. A case due to tuberculosis. 220
Erythema annulare centrifugum and Escherichia coli urinary infection. 220
Erythema annulare centrifugum following herpes zoster infection: Wolf’s isotopic response? 220
Erythema annulare centrifugum revealing chronic lymphocytic leukaemia. 220
Erythema annulare centrifugum as the presenting sign of breast carcinoma. 220
Erythema annulare centrifugum associated with mantle B-cell non-hodgkin’s lymphoma. 220
Erythema annulare centrifugum: a rare skin finding of autoimmune hepatitis. 220
Erythema annulare centrifugum as the presenting sign of the hypereosinophilic syndrome: observations on therapy. 220
Erythema annulare centrifugum-like mycosis fungoides. 220
Erythema annulare centrifugum following pancreatico-biliary surgery. 220
Linear IgA dermatosis presenting with erythema annulare centrifugum lesions: report of three cases in adults. 220
Erythema annulare centrifugum and relapsing polychondritis. 220
Erythema annulare centrifugum in a patient with polyglandular autoimmune disease type 1. 220
Pregnancy as a possible etiologic factor in erythema annulare centrifugum. 220
Autoimmune progesterone dermatitis manifested as erythema annulare centrifugum: confirmation of progesterone sensitivity by in vitro interferon-gamma release. 220
Contact erythema annulare centrifugum. 220
First-line therapies 220
Erythema annulare centrifugum caused by aldactone. 220
Ampicillin-induced erythema annulare centrifugum. 221
Erythema annulare centrifugum secondary to treatment with finasteride. 221
Erythema annulare centrifugum: an unusual case due to hydroxychloroquine sulfate. 221
Erythema annulare centrifugum. A case due to hypersensitivity to blue cheese Penicillium. 221
Erythema annulare centrifugum and Hodgkin’s disease: association with disease activity. 221
Erythema annulare centrifugum responding to natural ultraviolet light. 221
Second-line therapies 221
Annular erythema responding to tacrolimus ointment. 221
Third-line therapies 221
Erythema annulare centrifugum. 221
Calcipotriol for erythema annulare centrifugum. 221
Erythema annulare centrifugum successfully treated with metronidazole. 221
A novel therapeutic approach to erythema annulare centrifugum. 221
70 Erythema dyschromicum perstans 222
Management strategy 222
Specific investigations 222
Therapy 222
Erythema dyschromicum perstans in children: a report of 14 cases. 222
Vitamin A in the treatment of lichen planus pigmentosus. 222
Erythema dyschromicum perstans: response to dapsone therapy. 222
Erythema dyschromicum perstans in phototype II women: three unusual clinical cases studied with electron microscopy. 222
Erythema dyschromicum perstans: a case report and review. 222
Involvement of cell adhesion and activation molecules in the pathogenesis of erythema dyschromicum perstans (ashy dermatitis). The effect of clofazimine therapy. 222
71 Erythema elevatum diutinum 223
Management strategy 223
Specific investigations 223
Erythema elevatum diutinum: an ultrastructural case study. 223
Erythema elevatum diutinum: clinical, histopathologic, and immunohistochemical characteristics of six patients. 223
Erythema elevatum diutinum: a clinical and histopathologic study of 13 patients. 223
Erythema elevatum diutinum and IgA paraproteinaemia: ‘a preclinical iceberg’. 223
Is IgA antineutrophil cytoplasmic antibody a marker for patients with erythema elevatum diutinum? A further three cases demonstrating this association. 223
Erythema elevatum diutinum and HIV infection: a report of five cases. 224
Erythema elevatum diutinum associated with peripheral ulcerative keratitis. 224
Progressive keratolysis with pseudopterygium associated with erythema elevatum diutinum. 224
Erythema elevatum diutinum with verrucous carcinoma: a rare association. 224
Erythema elevatum diutinum associated with pyoderma gangrenosum in an HIV-positive patient. 224
Erythema elevatum diutinum in systemic lupus erythematosus. 224
First-line therapies 224
Erythema elevatum diutinum: a clinicopathological study. 224
Erythema elevatum diutinum with oral ulceration. 224
Alternative procedure to allow continuation of dapsone therapy despite serious adverse reaction in a case of dapsone-sensitive erythema elevatum diutinum. 224
A case of extensive erosive and bullous erythema elevatum diutinum in a patient diagnosed with human immunodeficiency virus (HIV). 224
Erythema elevatum diutinum with primary Sjögren syndrome associated with IgA antineutrophil cytoplasmic antibody. 224
Peripheral keratitis associated with erythema elevatum diutinum. 224
Erythema elevatum diutinum presenting with a giant annular pattern. 224
Nodular erythema elevatum diutinum in an HIV-1 infected woman: response to dapsone and antiretroviral therapy. 224
Nodular lesions of erythema elevatum diutinum in patients infected with the human immunodeficiency virus. 224
Successful combination therapy with dapsone and cyclosporine for erythema elevatum diutinum with unusual appearance. 225
Second-line therapies 225
Erythema elevatum diutinum treated with niacinamide and tetracycline. 225
Erythema elevatum diutinum: a case successfully treated with colchicine. 225
Third-line therapies 225
Erythema elevatum diutinum in association with coeliac disease. 225
Erythema elevatum diutinum in a patient with relapsing polychondritis. 225
Erythema elevatum diutinum associated with IgA paraproteinemia successfully controlled with intermittent plasma exchange. 225
Erythema elevatum diutinum after liver transplantation: disappearance of the lesions associated with a reduction in cyclosporine dosage. 225
Erythema elevatum diutinum: an unusual association with ulcerative colitis. 225
Erythema elevatum diutinum manifesting as a penile ulcer. 225
Erythema elevatum diutinum as a paraneoplastic syndrome in a patient with pulmonary lymphoepithelioma-like carcinoma. 225
72 Erythema multiforme 226
Management strategy 226
Specific investigations 226
First-line therapies 226
Recurrent erythema multiforme: clinical features and treatment in a large series of patients. 226
A double-blind, placebo-controlled trial of continuous acyclovir therapy in recurrent erythema multiforme. 226
Recurrent erythema multiforme unresponsive to acyclovir prophylaxis and responsive to valacyclovir continuous therapy. 226
Recurrent erythema multiforme: clinical characteristics, etiologic associations, and treatment in a series of 48 patients at Mayo Clinic, 2000 to 2007. 226
Erythema multiforme major associated with CMV infection in an immunocompetent patient. 227
Second-line therapies 227
Dapsone-responsive persistent erythema multiforme. 227
Characteristics of the oral lesions in patients with cutaneous recurrent erythema multiforme. 227
Azathioprine therapy in the management of persistent erythema multiforme. 227
Thalidomide for recurrent erythema multiforme. 227
Treatment by thalidomide of chronic multiforme erythema: its recurrent and continuous variants. A retrospective study of 26 patients. 227
Potassium iodide in erythema nodosum and other erythematous dermatoses. 227
Erythema multiforme – response to corticosteroid. 227
Oral EM 227
Open preliminary clinical trial of clobetasol propionate ointment in adhesive paste for treatment of chronic oral vesiculoerosive diseases. 227
Topically applied fluocinonide in an adhesive base in the treatment of oral vesiculoerosive diseases. 227
Erythema multiforme: diagnosis, clinical manifestations and treatment in a retrospective study of 22 patients. 227
Prednisone and azathioprine in the treatment of patients with vesiculoerosive oral diseases. 227
Recurrent oral erythema multiforme. Clinical experience with 11 patients. 227
Third-line therapies 227
Recurrent erythema multiforme: clinical features and treatment in a large series of patients. 228
Recurrent erythema multiforme and chronic hepatitis C: efficacy of interferon alpha. 228
Severe erythema multiforme responding to interferon alfa. 228
Progesterone-induced erythema multiforme. 228
Topical treatment of recurrent herpes simplex and post-herpetic erythema multiforme with low concentrations of zinc sulphate solution. 228
Cimetidine prevents recurrent erythema multiforme major resulting from herpes simplex virus infection. 228
Cyclosporine therapy for bullous erythema multiforme. 228
High-dose systemic corticosteroids can arrest recurrences of severe mucocutaneous erythema multiforme. 228
73 Erythema nodosum 229
Management strategies 229
Specific investigations 229
Erythema nodosum: a review. 229
Erythema nodosum and associated diseases: a study of 129 cases. 229
Erythema nodosum: a study of 160 cases. 229
Erythema nodosum: an evaluation of 100 cases. 229
First-line therapies 230
Suppression of erythema nodosum by indomethacin. 230
Chronic erythema nodosum treated with indomethacin. 230
Control of chronic erythema nodosum with naproxen. 230
Potassium iodide in erythema nodosum and other erythematous dermatoses. 230
Treatment of erythema nodosum and nodular vasculitis with potassium iodide. 230
Potassium iodide in dermatology. A 19th century drug for the 21st century: uses, pharmacology, adverse effects, and contraindications. 230
Second-line therapies 230
Traitement de l’erythème noueux par la colchicine. 230
Erythema nodosum treated with colchicine. 230
Hydroxychloroquine in the treatment of chronic erythema nodosum. 230
Hydroxychloroquine and chronic erythema nodosum. 230
Third-line therapies 230
Acne fulminans and erythema nodosum during isotretinoin therapy responding to dapsone. 230
Extracorporeal monocyte granulocytapheresis was effective for a patient of erythema nodosum concomitant with ulcerative colitis. 230
Severe erythema nodosum due to Behçet’s disease responsive to erythromycin. 231
Use of mycophenolate mofetil in erythema nodosum. 231
Dermatologic manifestations of Crohn disease in children: response to infliximab. 231
Treatment of chronic erythema nodosum with infliximab. 231
Etanercept treatment of erythema nodosum. 231
Prophylaxis of recurrent erythema nodosum with penicillin. 231
Refractory chronic erythema nodosum successfully treated with adalimumab. 231
Successful treatment of chronic erythema nodosum with vitamin B12. 231
Response of recalcitrant erythema nodosum to tetracyclines. 231
74 Erythrasma 232
Management strategy 232
Specific investigations 232
First-line therapies 232
A comparison between the effectiveness of erythromycin, single dose clarithromycin and topical fusidic acid in the treatment of erythrasma. 232
Treatment of erythrasma with miconazole. 232
A clinical double-blind trial of topical miconazole and clotrimazole against superficial fungal infections and erythrasma. 232
Topical treatment for erythrasma. 232
Second-line therapies 232
Systemic or local treatment of erythrasma? A comparison between erythromycin tablets and Fucidin cream in general practice. 232
A comparison between the effectiveness of erythromycin, single dose clarithromycin and topical fusidic acid in the treatment of erythrasma. 233
Erythrasma treated with single-dose clarithromycin. 233
The treatment of erythrasma in a hospital for the mentally subnormal. 233
Antibiotic susceptibility of Corynebacterium minutissimum isolated from lesions of Turkish patients with erythrasma. 233
75 Erythroderma 234
Management strategy 234
Specific investigations 234
Diagnosing erythrodermic cutaneous T-cell lymphoma. 235
Survival outcomes and prognostic factors in mycosis fungoides/Sézary syndrome: validation of the revised International Society for Cutaneous Lymphomas/European Organisation for Research and Treatment of Cancer staging proposal. 235
Erythrodermic bullous pemphigoid. 235
A case of erythrodermic dermatomyositis associated with gastric cancer. 235
Subacute cutaneous lupus erythematosus presenting as erythroderma. 235
Idiopathic erythroderma: a follow-up study of 28 patients. 235
Inherited ichthyoses: a review of the histology of the skin. 235
Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas. 235
Congenital erythrodermic psoriasis: case report and literature review. 235
Erythroderma due to dermatophyte. 235
Erythroderma as the initial presentation of the acquired immunodeficiency syndrome. 235
First-line therapies 236
Second-line therapies 236
Cushing’s syndrome caused by short-term topical glucocorticoid use for erythrodermic psoriasis and development of adrenocortical insufficiency after glucocorticoid withdrawal. 236
Salicylism from topical salicylates: review of the literature. 236
Hypercalcemia caused by vitamin D3 analogs in psoriasis treatment. 236
Low but detectable serum levels of tacrolimus seen with the use of very dilute, extemporaneously compounded formulations of tacrolimus ointment in the treatment of patients with Netherton syndrome. 236
Ofuji’s papuloerythroderma: a study of 17 cases. 236
Treatment of papuloerythroderma of Ofuji with Re-PUVA: a case report and review of the therapy. 236
A dermatitis–eosinophilia syndrome. Treatment with methylprednisolone pulse therapy. 236
Toxic shock syndrome responsive to steroids. 236
Third-line therapies 236
Management of erythrodermic psoriasis with low-dose cyclosporine. 236
Papuloerythroderma of Ofuji responding to treatment with cyclosporine. 236
Psoriatic erythroderma and bullous pemphigoid treated successfully with acitretin and azathioprine. 236
Methotrexate in psoriasis: 26 years’ experience with low-dose long-term treatment. 236
Systemic methotrexate treatment in childhood psoriasis: further experience in 24 children from India. 236
An appraisal of acitretin therapy in children with inherited disorders of keratinization. 236
Treatment of classic pityriasis rubra pilaris. 237
Treatment of refractory adult-onset pityriasis rubra pilaris with TNF-alpha antagonists: a case series. 237
Evidence-based practice of photopheresis 1987–2001: a report of a workshop of the British Photodermatology Group and the UK Skin Lymphoma Group. 237
Extracorporeal photopheresis in Sézary syndrome: hematologic parameters as predictors of response. 237
U.K. consensus statement on the use of extracorporeal photopheresis for treatment of cutaneous T-cell lymphoma and chronic graft-versus-host disease. 237
Treatment of severe erythrodermic acute graft-versus- host disease with photochemotherapy. 237
‘High-dose’ UVA1 therapy of widespread plaque-type, nodular, and erythrodermic mycosis fungoides. 237
Bullous congenital ichthyosiform erythroderma: safe and effective topical treatment with calcipotriol ointment in a child. 237
Successful treatment of Netherton’s syndrome with topical calcipotriol. 237
Efficacy and safety of tacrolimus 0.03% ointment in a 1-month-old ‘red baby’: a case report. 237
Erythrodermic chronic actinic dermatitis responding to topical tacrolimus. 237
Successful treatment of bullous congenital ichthyosiform erythroderma with erythromycin. 237
Combination therapy with extracorporeal photophoresis, interferon-alpha, PUVA and topical corticosteroids in the management of Sézary syndrome. 237
Efficacy and safety of biologics in erythrodermic psoriasis: a multicentre, retrospective study. 237
A follow-up study in 28 patients treated with infliximab for severe recalcitrant psoriasis: evidence for efficacy and high incidence of biological autoimmunity. 237
Infliximab as sole or combined therapy, induces rapid clearing of erythrodermic psoriasis. 237
Treatment of erythrodermic psoriasis with etanercept. 238
Alemtuzumab for relapsed and refractory erythrodermic cutaneous T-cell lymphoma: a single institution experience from the Robert H Lurie Comprehensive Cancer Center. 238
Novel treatment of Sézary-like syndrome due to adult T-cell leukaemia/lymphoma with daclizumab (humanized anti-interleukin-2 receptor alpha antibody). 238
The treatment of cutaneous T-cell lymphoma with a novel retinoid. 238
Bexarotene therapy for mycosis fungoides and Sézary syndrome. 238
76 Erythrokeratodermas 239
Management strategy 239
Specific investigations 239
Connexin disorders of the skin. 239
The missense mutation G12D in connexin 30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. 240
Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetric erythrokeratodermia. 240
First-line therapies 240
Erythrokeratodermia variabilis successfully treated with topical tazarotene. 240
Erythrokeratodermia variabilis. Report of 3 clinical cases and evaluation of the topical retinoic acid treatment. 240
[Progressive symmetrische erythrokeratodermie Darier-Gottron]. 240
Erythrokeratodermia variabilis. Case report and review of the literature. 240
Second-line therapies 240
Clinical and genetic heterogeneity of erythrokeratodermia variabilis. 240
Erythrokeratodermia variabilis caused by a recessive mutation in GJB3. 240
Erythrokeratodermia variabilis. 240
Erythrokeratoderma variabilis responding to low- dose isotretinoin. 240
Erythrokeratodermia variabilis with adult onset: report of a sporadic case unresponsive to systemic retinoids. 240
Third-line therapies 241
Erythrokeratodermia variabilis: successful treatment with retinoid plus psoralen and ultraviolet A therapy. 241
Gottron’s erythroderma congenitalis progressiva symmetrica. 241
Erythrokeratodermia variabilis: case report and review of literature. 241
77 Erythromelalgia 242
Management strategy 242
Specific investigations 242
Nonspecific capillary proliferation and vasculopathy indicate skin hypoxia in erythromelalgia. 242
Platelet-mediated erythromelalgic, cerebral, ocular and coronary microvascular ischemic and thrombotic manifestations in patients with essential thrombocythemia and polycythemia vera: a distinct aspirin-responsive and coumadin- resistant arterial thrombophilia. 242
Erythromelalgia – a thrombotic complication in chronic myeloproliferative disorders. 242
First-line therapies 243
Aspirin-responsive painful red, blue, black toe, or finger-syndrome in polycythemia vera associated with thrombocythemia. 243
The Erythromelalgia Association Survey 2003. 243
Erythromelalgia – a condition caused by microvascular arteriovenous shunting. 243
Prostacyclin reduces symptoms and sympathetic dysfunction in erythromelalgia in a double-blind randomized pilot study. 243
The prostaglandin E1 analog misoprostol reduces symptoms and microvascular arteriovenous shunting in erythromelalgia – a double-blind, crossover, placebo- compared study. 243
Second-line therapies 243
Treatment of Nav1.7-mediated pain in inherited erythromelalgia using novel sodium channel blocker. 243
Primary erythromelalgia in a 12-year-old boy: positive response to sodium channel blockers despite negative SCN9A mutations. 243
Primary erythromelalagia in a child responding to intravenous lidocaine and oral mexiletine treatment. 243
Lidocaine patch for pain of erythromelalgia: follow-up of 34 patients. 243
Pediatric erythromelalgia: a retrospective review of 32 cases evaluated at Mayo Clinic over a 37-year period. 243
A case of erythromelalgia: good response to treatment with gabapentin. 243
Treatment of familial erythromelalgia with venlafaxine. 244
Combination gel of 1% amitriptyline and 0.5% ketamine to treat refractory erythromelalgia pain: a new treatment option? 244
Erythromelalgia – a condition caused by microvascular arteriovenous shunting. 244
Third-line therapies 244
Erythromelalgia: new theories and new therapies. 244
High-dose oral magnesium treatment of chronic, intractable erythromelalgia. 244
Erythromelalgia. 244
78 Erythropoietic protoporphyria 245
Management strategy 245
Specific investigations 245
Erythropoietic protoporphyria. 245
Hepatobiliary implications and complications in protoporphyria. A 20-year study. 245
First-line therapies 245
Efficiency of opaque photoprotective agents in the visible light range. 245
Erythropoietic protoporphyria: IV. Protection from sunlight. 245
Beta-carotene therapy for erythropoietic protoporphyria and other photosensitivity diseases. 245
Second-line therapies 246
Narrow-band (TL-01) UVB phototherapy: an effective preventative treatment for the photodermatoses. 246
Photo(chemo)therapy and general management of erythropoietic protoporphyria. 246
Third-line therapies 246
An alpha-melanocyte-stimulating hormone analogue in erythropoietic protoporphyria. 246
Long-term treatment of erythropoietic protoporphyria with cysteine. 246
Inhibition of photosensitivity in erythropoietic protoporphyria with terfenadine. 246
Cimetidine reduces erythrocyte protoporphyrin in erythropoietic protoporphyria. 246
A case of erythropoietic protoporphyria with liver cirrhosis suggesting a therapeutic value of supplementation with alpha-tocopherol. 246
A double-blind, placebo-controlled, crossover trial of oral vitamin C in erythropoietic protoporphyria. 246
Relief of the photosensitivity of erythropoietic protoporphyria by pyridoxine. 246
Treatment of erythropoietic protoporphyria with hydroxyethylrutosides. 246
Iron therapy for hepatic dysfunction in erythropoietic protoporphyria. 246
Symptomatic response of erythropoietic protoporphyria to iron supplementation. 247
Erythropoietic protoporphyria and iron therapy. 247
Fecal protoporphyrin excretion in erythropoietic protoporphyria: effect of cholestyramine and bile acid feeding. 247
Liver failure in protoporphyria: long-term treatment with oral charcoal. 247
Liver disease in erythropoietic protoporphyria: insights and implications for management. 247
Liver transplantation for erythropoietic protoporphyria liver disease. 247
Liver transplantation for erythropoietic protoporphyria in Europe. 247
Perioperative measures during liver transplantation for erythropoietic protoporphyria. 247
The value of intravenous heme-albumin and plasmapheresis in reducing postoperative complications of orthotopic liver transplantation for erythropoietic protoporphyria. 247
Treatment of recurrent allograft dysfunction with intravenous hematin after liver transplantation for erythropoietic protoporphyria. 247
Erythropoietic protoporphyria: altered phenotype after bone marrow transplantation for myelogenous leukemia in a patient heteroallelic for ferrochelatase gene mutations. 247
Sequential liver and bone marrow transplantation for treatment of erythropoietic protoporphyria. 247
Curative bone marrow transplantation in erythropoietic protoporphyria after reversal of severe cholestasis. 247
79 Extramammary Paget disease 248
Management strategy 248
Specific investigations 248
Extramammary Paget’s disease: treatment, prognostic factors and outcome in 76 patients. 248
Epidemiology and treatment of EMPD in the Netherlands. 248
First-line therapies 249
Indications for lymph node dissection in the treatment of EMPD. 249
Clinicopathological study of invasive extramammary Paget’s disease: subgroup comparison according to invasion depth. 249
Penile and scrotal Paget’s disease: experiences from 130 Chinese patients with a long-term follow-up. 249
Frozen section-guided wide local excision in the treatment of penoscrotal EMPD. 249
EMPD: surgical treatment with Mohs micrographic surgery. 249
Comparison of Mohs micrographic surgery and wide excision for EMPD. 249
Second-line therapies 249
Photodynamic therapy using a methyl ester of 5-aminolevulinic acid in recurrent Paget’s disease of the vulva: a pilot study. 249
Effectiveness of photodynamic therapy for mammary and extramammary Paget’s disease: a state of the science review. 249
Metastatic EMPD successfully controlled with tumour dormancy therapy using docetaxel. 249
A case of metastatic extramammary Paget’s disease responding to trastuzumab plus paclitaxel combination therapy. 249
Trial of low-dose 5-fluorouracil/cisplatin therapy for advanced EMPD. 250
Low-dose mitomycin C, etoposide, and cisplatin for invasive vulvar Paget’s disease. 250
Definitive radiation therapy for extramammary Paget’s disease. 250
Complete resolution of Paget’s disease of the vulva with imiquimod cream. 250
Treatment of vulvar Paget disease with topical imiquimod: a case report and review of the literature. 250
Third-line therapies 250
EMPD resistant to surgery and imiquimod monotherapy but responsive to imiquimod combination topical chemotherapy with 5-fluorouracil and retinoic acid: a case report. 250
Intralesional interferon alfa-2b as neoadjuvant treatment for perianal EMPD. 250
Failure of carbon dioxide laser treatment in three patients with penoscrotal EMPD. 250
Estrogen-receptor-alpha-positive EMPD treated with hormonal therapy. 250
Androgen-deprivation regimen for multiple bone metastases of EMPD. 250
80 Fabry disease 251
Management strategy 251
Specific investigations 252
Angiokeratoma: decision making aid for the diagnosis of Fabry disease. 252
Treatment of Fabry disease: current and emerging strategies. 252
Fabry disease and the skin: data from FOS, the Fabry Outcome Survey. 252
81 Flushing 255
Management strategy 255
Specific investigations 255
The red face: flushing disorders. 255
Flushing reactions in the chemotherapy patient. 255
Flushing reactions. 255
Influence of a serotonin- and dopamine-rich diet on platelet serotonin content and urinary excretion of biogenic amines and their metabolites. 255
Serotonin, catecholamines, histamine, and their metabolites in urine, platelets, and tumor tissue of patients with carcinoid tumors. 255
Comparison of clinical trials with sildenafil, vardenifil and tadalafil in erectile dysfunction. 255
First-line therapies 256
Oral thermal-induced flushing in erythematotelangiectatic rosacea. 256
Aspirin blocks nicotinic acid-induced flushing. 256
Aspirin attenuation of alcohol-induced flushing and intoxication in Oriental and Occidental subjects. 256
Combined versus sequential hormonal replacement therapy: a double-blind, placebo-controlled study on quality of life-related outcome measures. 256
Second-line therapies 256
Scombroid fish poisoning, Pennsylvania, 1998. 256
Histamine receptor antagonism of intolerance to alcohol in the Oriental population. 256
Primary care for survivors of breast cancer. 256
Phytoestrogens for vasomotor menopausal symptoms. 256
Nonhormonal therapies for menopausal hot-flashes. 256
Treatment strategies for reducing the burden of menopause-associated vasomotor symptoms. 256
Third-line therapies 257
Treatment of type II gastric carcinoid tumors with somatostatin analogues. 257
Management of facial flushing. 257
Carvedilol for the treatment of refractory facial flushing and persistent erythema of rosacea. 257
Symptomatic treatment of idiopathic and rosacea-associated cutaneous flushing with propranolol. 257
Successful treatment of the erythema and flushing of rosacea using a topically applied selective alpha 1-adrenergic receptor agonist, oxymetazoline. 257
82 Follicular mucinosis 258
Management strategy 258
Specific investigations 258
The cutaneous mucinoses. 258
Follicular mucinosis: a clinicopathologic, histochemical, immunohistochemical and molecular study comparing the primary benign form and the mycosis fungoides-associated follicular mucinosis. 258
First-line therapies 258
Follicular mucinosis: a study of 47 patients. 258
Neonatal follicular mucinosis. 258
Urticaria-like follicular mucinosis responding to dapsone. 258
Atypical follicular mucinosis controlled with mepacrine. 258
A case of follicular mucinosis treated successfully with minocycline. 259
Second-line therapies 259
Follicular mucinosis presenting as an acneiform eruption: report of four cases. 259
Follicular mucinosis treated with PUVA. 259
Treatment of idiopathic mucinosis follicularis with UVA1 cold light phototherapy. 259
Follicular mucinosis: response to indomethacin. 259
Successful treatment of recalcitrant primary follicular mucinosis with indomethacin and low-dose intralesional interferon alpha. 259
Acneiform follicular mucinosis. 259
Alopecia mucinosa: a follow-up study. 259
Primary follicular mucinosis: excellent response to treatment with photodynamic therapy. 259
Treatment of so-called idiopathic follicular mucinosis with hydroxychloroquine. 259
Follicular mucinosis treated with tacrolimus. 259
A case of follicular mucinosis treated successfully with pimecrolimus. 259
83 Folliculitis 260
Management strategy 260
Specific investigations 260
First-line therapies 260
Topical therapy 261
Topical retapamulin ointment, 1%, versus sodium fusidate ointment, 2%, for impetigo: a randomized, observer-blinded, noninferiority study. 261
A randomized, controlled trial of tea tree topical preparations versus a standard topical regimen for the clearance of MRSA colonization. 261
Refractory Demodex folliculitis in five children with acute lymphoblastic leukemia. 261
Recalcitrant papulopustular rosacea in an immunocompetent patient responding to combination therapy with oral ivermectin and topical permethrin. 261
Successful treatment of eosinophilic pustular folliculitis with topical tacrolimus 0.1% ointment. 261
Systemic therapy 261
Treatment of MRSA soft tissue infections: an overview. 261
Hot tub folliculitis or hot hand-foot syndrome caused by Pseudomonas aeruginosa. 261
Skin diseases associated with Malassezia species. 261
Therapeutic effectiveness of various treatments for eosinophilic pustular folliculitis. 261
Folliculitis induced by EGFR inhibitors, preventive and curative efficacy of tetracyclines in the management and incidence rates according to the type of EGFR inhibitor administered: a systematic literature review. 261
Second-line therapies 261
Efficacy and safety of tigecycline compared with vancomycin or linezolid for treatment of serious infections with methicillin-resistant Staphylococcus aureus or vancomycin-resistant Enterococci: a phase III, multicenter, double-blind, randomized study. 261
Intramuscular immunoglobulin for recalcitrant suppurative diseases of the skin: a retrospective review of 63 cases. 261
Topical methyl aminolevulinate photodynamic therapy for the treatment of folliculitis. 262
Malassezia folliculitis: characteristics and therapeutic response in 26 patients. 262
84 Folliculitis decalvans 263
Management strategy 263
Specific investigations 263
Acquired scalp alopecia. Part II: A review. 263
Folliculitis decalvans and cellular immunity – 2 brothers with oral candidiasis. 263
Tufted folliculitis of the scalp; a distinctive clinicohistological variant of folliculitis decalvans. 263
Tinea capitis mimicking folliculitis decalvans. 263
First-line therapies 263
Management of primary cicatricial alopecias: options for treatment. 263
Folliculitis decalvans including tufted folliculitis: clinical, histological and therapeutic findings. 263
Tufted folliculitis of the scalp: a distinctive clinicohistological variant of folliculitis decalvans. 264
Folliculitis decalvans – response to rifampicin. 264
Second-line therapies 264
Folliculitis decalvans. 264
Dapsone treatment of folliculitis decalvans. 264
Simultaneous occurrence of folliculitis decalvans capillitii in identical twins. 264
Treatment of folliculitis decalvans with tacrolimus ointment. 264
Third-line therapies 264
Tufted hair folliculitis. 264
Tufted hair folliculitis. A study of 4 cases. 264
Folliculitis decalvans treated with radiation therapy. 264
Nd : YAG laser treatment of recalcitrant folliculitis decalvans. 264
Successful use of infliximab in a patient with recalcitrant folliculitis decalvans. 264
85 Fox–Fordyce disease 265
Management strategy 265
Specific investigations 265
Fox–Fordyce disease: diagnosis by transverse histologic sections. 265
Patterns histopathologic of Fox–Fordyce disease. 265
Dilation of apocrine glands. A forgotten but helpful histopathological clue to the diagnosis of axillary Fox–Fordyce disease. 265
Clinicopathological study of Fox–Fordyce disease. 265
Axillary perifollicular xanthomatosis resembling Fox–Fordyce disease. 265
Perifollicular xanthomatosis as a key histological finding in Fox–Fordyce disease. 265
First-line therapies 265
A new treatment of Fox–Fordyce disease. 265
Fox–Fordyce disease – successful treatment with topical clindamycin in alcoholic propylene glycol solution. 266
Fox–Fordyce disease. Treatment with an oral contraceptive. 266
Fox–Fordyce disease. Control with tretinoin cream. 266
Treatment of Fox–Fordyce disease. 266
Pimecrolimus is effective in Fox–Fordyce disease. 266
The treatment of Fox–Fordyce disease. 266
Second-line therapies 266
Fox–Fordyce disease in a male patient – response to oral retinoid treatment. 266
Fox–Fordyce disease in the post-menopausal period treated successfully with electrocoagulation. 266
Surgical treatment of areolar hidradenitis suppurativa and Fox–Fordyce disease. 266
Axillary Fox–Fordyce disease treated with liposuction-assisted curettage. 266
86 Furunculosis 267
Management strategy 267
Specific investigations 267
First-line therapies 267
Randomized, double-blind, placebo-controlled trial of cephalexin for treatment of uncomplicated skin abscesses in a population at risk for community-acquired methicillin-resistant Staphylococcus aureus infection. 267
Second-line therapies 267
Clinical practice guidelines by the Infectious Diseases Society of America for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary. 268
Tetracyclines as an oral treatment option for patients with community onset skin and soft tissue infections caused by methicillin-resistant Staphylococcus aureus. 268
Prevalence, severity, and treatment of community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) skin and soft tissue infections in 10 medical clinics in Texas: a South Texas Ambulatory Research Network (STARNet) study. 268
Trimethoprim-sulfamethoxazole or clindamycin for treatment of community-acquired methicillin-resistant Staphylococcus aureus skin and soft tissue infections. 268
Third-line therapies/prevention 268
Randomized controlled trial of chlorhexidine gluconate for washing, intranasal mupirocin, and rifampin and doxycycline versus no treatment for the eradication of methicillin-resistant Staphylococcus aureus colonization. 268
Prospective investigation of nasal mupirocin, hexachlorophene body wash, and systemic antibiotics for prevention of recurrent community-associated methicillin-resistant Staphylococcus aureus infections. 268
Hypochlorite killing of community- associated methicillin-resistant Staphylococcus aureus. 268
Recurrent staphylococcal infection in families. 268
In vitro activity of retapamulin against Staphylococcus aureus isolates resistant to fusidic acid and mupirocin. 268
Treatment and prevention of recurrent staphylococcal furunculosis: clinical and bacteriological follow-up. 268
87 Geographic tongue 269
Management strategy 269
Specific investigations 269
Geographic stomatitis: a critical review. 269
First-line therapies 269
Symptomatic benign migratory glossitis: report of two cases and literature review. 269
Common tongue conditions in primary care. 269
Glossitis and other tongue disorders. 269
Painful geographic tongue (benign migratory glossitis) in a child. 269
Second-line therapies 269
Glossodynia and other disorders of the tongue. 269
The treatment of geographic tongue with topical retin-A solution. 270
Geographic tongue treated with topical tacrolimus. 270
Third-line therapies 270
Successful treatment with cyclosporine administration for persistent benign migratory glossitis. 270
88 Gianotti–Crosti syndrome 271
Management strategy 271
Specific investigations 271
Gianotti–Crosti syndrome associated with transfusion acquired hepatitis B virus infection in a patient of sickle cell anemia. 271
Gianotti–Crosti syndrome in a child following hepatitis B virus vaccination. 272
Gianotti-Crosti syndrome after childhood vaccination. 272
Gianotti-Crosti syndrome following novel influenza A (H1N1) vaccination. 272
Gianotti–Crosti syndrome. 272
Atypical Gianotti–Crosti syndrome in two HIV and hepatitis B co-infected adults. 272
Gianotti–Crosti syndrome and allergic background. 272
First-line therapies 272
Acute disseminated erythematous papulovesicular skin lesions in a 7-year-old child: a quiz. Diagnosis: vesicular Gianotti–Crosti syndrome. 272
Recurrent Gianotti–Crosti syndrome. 272
Second-line therapies 272
Infantile acrodermatitis of Gianotti–Crosti and Lyme borreliosis. 272
Efficacy of ribavirin in a case of long lasting and disabling Gianotti–Crosti syndrome. 272
89 Gonorrhea 273
Management strategy 273
Specific investigations 273
Male urethritis with and without discharge. A clinical and microbiological study. 273
Sexually transmitted diseases treatment guidelines 2010. 273
Screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections – 2002. 273
A laboratory-based evaluation of the BioStar Optical ImmunoAssay point-of-care test for diagnosing Neisseria gonorrhoeae infection. 274
First-line therapies 274
Oral cefixime versus intramuscular ceftriaxone in patients with uncomplicated gonococcal infections. 274
Sexually transmitted diseases treatment guidelines 2010. 274
First Neisseria gonorrhoeae strain with resistance to cefixime causing gonorrhoea treatment failure in Austria, 2011. 274
UK national guideline for the management of gonorrhoea in adults, 2011. 274
Second-line therapies 274
Update on the management of gonorrhea in adults in the United States. 274
Which cephalosporin for gonorrhoea? 274
Third-line therapies 274
Neisseria gonorrhoeae with high-level resistance to azithromycin: case report of the first isolate identified in the United States. 274
Spectinomycin resistance in Neisseria spp. due to mutations in IGSrRNA. 274
Update to CDC’s sexually transmitted diseases treatment guidelines 2006: fluoroquinolones no longer recommended for treatment of gonococcal infections. 274
Surveillance of antibiotic resistance in Neisseria gonorrhoeae in the WHO Western Pacific and South East Asian Regions, 2009. 275
Annual report of the Australian Gonococcal Surveillance Programme, 2010. 275
Cephalosporin resistant Neisseria gonorrhoeae: time to consider gentamicin? 275
Special considerations 275
Pharyngeal infection 275
Treating uncomplicated Neisseria gonorrhoeae infections: is the anatomic site of infection important? 275
Disseminated gonococcal infection 275
Pregnancy 275
Treatment of gonorrhoea in pregnancy. 275
Ophthalmia neonatorum 275
Men who have sex with men 275
Gonorrhea screening among men who have sex with men: value of multiple anatomic site testing, San Diego, California, 1997–2003. 275
Treatment failure 275
90 Graft-versus-host disease 276
Management strategy 276
Acute gvhd 276
Specific investigations 276
Clinical differentiation of acute cutaneous graft-versus-host disease from drug hypersensitivity reactions. 276
Role of skin biopsy to confirm suspected acute graft-vs-host disease: results of decision analysis. 276
Acute graft-versus-host disease biomarkers measured during therapy can predict treatment outcomes: a Blood and Marrow Transplant Clinical Trials Network Study. 277
First-line therapies 277
Early treatment of acute graft-versus-host disease with high- or low-dose 6-methylprednisolone: a multicenter randomized trial from the Italian Group for Bone Marrow Transplantation. 277
First- and second-line systemic treatment of acute graft-versus-host disease: recommendations of the American Society of Blood and Marrow Transplantation. 277
Second-line therapies 277
Steroid-refractory acute GVHD: lack of long-term improved survival using new generation anticytokine treatment. 277
Etanercept, mycophenolate, denileukin, or pentostatin plus corticosteroids for acute graft-versus-host disease: a randomized phase 2 trial from the Blood and Marrow Transplant Clinical Trials Network. 277
Role of extracorporeal photopheresis (ECP) in treatment of steroid-refractory acute graft-versus-host disease. 277
A phase III study of infliximab and corticosteroids for the initial treatment of acute graft-versus-host disease. 277
Etanercept plus methylprednisolone as initial therapy for acute graft-versus-host disease. 277
Inflammatory cytokine inhibition with combination daclizumab and infliximab for steroid-refractory acute GVHD. 277
Sirolimus for treatment of steroid-refractory acute graft-versus-host disease. 277
Third-line therapies 277
Diagnosis and management of acute graft-versus-host disease. 278
Narrowband ultraviolet B phototherapy for treatment of steroid-refractory and steroid-dependent acute graft-versus-host disease. 278
Chronic gvhd 278
Specific investigations 278
91 Granuloma annulare 280
Management strategy 280
Specific investigations 280
Carbohydrate tolerance in patients with granuloma annulare. Study of fifty two cases. 280
Absence of carbohydrate intolerance in patients with granuloma annulare. 280
Localised granuloma annulare is associated with insulin-dependent diabetes mellitus. 280
Localized granuloma annulare 280
First-line therapies 280
Granuloma annulare and necrobiosis lipoidica treated by jet injector. 280
Successful outcome of cryosurgery in patients with granuloma annulare. 280
Successful treatment of chronic skin diseases with clobetasol propionate and a hydrocolloid occlusive dressing. 281
Second-line therapies 281
Treatment of granuloma annulare with the 595 nm pulsed dye laser (PDL), a multicentre retrospective study with long-term follow-up. 281
Photodynamic therapy for granuloma annulare: more than a shot in the dark. 281
Successful treatment of granuloma annulare with imiquimod cream 5%: a report of four cases. 281
Granuloma annulare: dramatically altered appearance after application of 5% imiquimod cream. 281
Multiple localized granuloma annulare: ultraviolet A1 phototherapy. 281
Treatment of granuloma annulare by local injections with low dose recombinant human interferon gamma. 281
Scarification treatment of granuloma annulare. 281
Surgical pearl: surgical treatment of tumour sized granuloma annulare of the fingers. 281
Granuloma annulare treated with rifampin, ofloxacin, and minocycline combination therapy. 281
Generalized granuloma annulare 281
First-line therapies 281
UVA1 phototherapy for disseminated granuloma annulare. 281
Resolution of disseminated granuloma annulare with isotretinoin. 281
The response of generalised granuloma annulare to dapsone. 281
Successful treatment of disseminated granuloma annulare with topical tacrolimus. 281
Successful treatment of perforating granuloma annulare with 0.1% tacrolimus ointment. 282
Generalized granuloma annulare treated with methylaminolevulinate photodynamic therapy. 282
Second-line therapies 282
Psoralen and ultraviolet A in the treatment of granuloma annulare. 282
Clearance of generalized papular umbilicated granuloma annulare in a child with bath PUVA therapy. 282
Treatment of disseminated granuloma annulare with low dose fumaric acid. 282
Treatment of disseminated granuloma annulare recalcitrant to topical therapy: a retrospective 10 year analysis with comparison of photochemotherapy alone versus photochemotherapy plus oral fumaric acid esters. 282
Antimalarials for control of disseminated granuloma annulare in children. 282
A contact dermatitis reaction to clobetasol propionate cream associated with resolution of recalcitrant, generalised granuloma annulare. 282
Granuloma annulare, generalised. 282
Low dose chlorambucil in the treatment of generalised granuloma annulare. 282
Disseminated granuloma annulare: efficacy of cyclosporine therapy. 282
Treatment of recalcitrant disseminated granuloma annulare with hydroxyurea. 282
Generalized granuloma annulare: response to doxycycline. 282
Fractional photothermolysis for the treatment of granuloma annulare: a case report. 282
Pimecrolimus 1% cream in the treatment of disseminated granuloma annulare. 283
A case of generalized granuloma annulare with myelodysplastic syndrome: successful treatment with systemic isotretinoin and topical pimecrolimus 1% cream combination. 283
Generalized interstitial granuloma annulare: response to adalimumab. 283
Disseminated granuloma annulare: a cutaneous adverse effect of anti-tnf agents. 283
Treatment of disseminated granuloma annulare with allopurinol: case report. 283
Response of generalized granuloma annulare to high-dose niacinamide. 283
Generalised granuloma annulare successfully treated with pentoxifylline. 283
A case of disseminated granuloma annulare treated with defibrotide: complete clinical remission and progressive hair darkening. 283
Disseminated granuloma annulare: therapy with vitamin E topically. 283
Treatment of disseminated granuloma annulare with anthralin. 283
92 Granuloma faciale 284
Management strategy 284
Specific investigations 284
Granuloma faciale: a clinicopathologic study of 66 patients. 284
First-line therapies 284
Granuloma faciale treated with intradermal dexamethasone. 284
Assessment of the efficacy of cryosurgery in the treatment of granuloma faciale. 284
Granuloma faciale: successful treatment of nine cases with a combination of cryotherapy and intralesional corticosteroid injection. 284
Granuloma faciale treated with pulsed-dye laser: a case series. 284
New treatment modalities for granuloma faciale. 285
Granuloma faciale: treatment with the argon laser. 285
Carbon dioxide laser treatment of granuloma faciale. 285
Recurrent facial plaques following full-thickness grafting. 285
Granuloma faciale: comparison of different treatment modalities. 285
Second-line therapies 285
On the efficacy of dapsone in granuloma faciale. 285
Granuloma faciale: is it a new indication for pimecrolimus? A case report. 285
Granuloma faciale: treatment with topical tacrolimus. 285
Third-line therapies 285
Granuloma faciale mimicking rhinophyma: response to clofazimine. 285
Granuloma faciale: treatment with topical psoralen and UVA. 285
93 Granuloma inguinale 286
Management strategy 286
Specific investigations 286
Genital ulcer disease: accuracy of clinical diagnosis and strategies to improve control in Durban, South Africa. 286
Donovanosis. 286
Sexually transmitted disease surveillance 2010. 286
Culture of the causative organism of donovanosis (Calymmatobacterium granulomatis) in Hep-2 cells. 286
A colorimetric detection system for Calymmatobacterium granulomatis. 286
First-line therapies 286
Donovanosis: treatment with azithromycin. 286
2010 European guideline on donovanosis. 287
Sexually transmitted diseases treatment guidelines 2010. 287
Second-line therapies 287
Clinico-epidemiologic features of granuloma inguinale in the era of acquired immune deficiency syndrome. 287
Granuloma inguinale. 287
Third-line therapies 287
Ceftriaxone in the treatment of chronic donovanosis in Central Australia. 287
1998 Guidelines for treatment of sexually transmitted diseases. 287
Surgical treatment of granuloma inguinale. 287
Treatment of donovanosis with norfloxacin. 287
Trovofloxacin for the treatment of chronic granuloma inguinale. 287
The diagnosis and treatment of donovanosis (granuloma inguinale). 287
Donovanosis in Papua New Guinea. 287
Donovanosis treated with thiamphenicol. 287
Special considerations 287
94 Granulomatous cheilitis 288
Management strategy 288
Specific investigations 288
Characteristics of patients with orofacial granulomatosis. 289
Melkersson–Rosenthal syndrome: a review of 36 patients. 289
Cheilitis granulomatosa. 289
Orofacial granulomatosis. 289
Cheilitis granulomatosa: overview of 13 patients with long-term follow-up: results of management. 289
Orofacial granulomatosis: clinical features and long-term outcome of therapy. 289
Anesthetic management of patients with Melkersson Rosenthal syndrome. 289
Is orofacial granulomatosis in children a feature of Crohn’s disease? 289
Re: Melkersson–Rosenthal syndrome as an early manifestation of Crohn’s disease. 289
Orofacial granulomatosis in a patient with Crohn’s disease. 289
Cheilitis granulomatosa and Melkersson–Rosenthal syndrome: evaluation of gastrointestinal involvement and therapeutic regimens in 14 patients. 289
Orofacial granulomatosis as the initial presentation of Crohn’s disease in an adolescent. 289
Cutaneous Crohn’s disease mimicking Melkersson– Rosenthal syndrome: treatment with methotrexate. 289
Asymptomatic granulomatous vulvitis and granulomatous cheilitis in childhood: the need for Crohn disease workup. 289
Orofacial granulomatosis: three case reports illustrating the spectrum of disease and overlap with Crohn’s disease. 289
Melkersson–Rosenthal syndrome and cheilitis granulomatosa. A clinicopathologic study of thirty-three patients with special reference to their oral lesions. 289
Review article: orofacial granulomatosis. 289
The Melkersson–Rosenthal syndrome and food additive hypersensitivity. 289
Contact hypersensitivity in patients with orofacial granulomatosis. 289
Patch testing for food-associated allergies in orofacial granulomatosis. 289
First-line therapies 289
Management of cheilitis granulomatosa. 289
Intralesional steroid injection after nerve block anesthesia in the treatment of orofacial granulomatosis. 290
Melkersson–Rosenthal syndrome and orofacial granulomatosis. 290
Second-line therapies 290
Clofazimine as elective treatment for granulomatous cheilitis. 290
Cheilitis granulomatosa Miescher: treatment with clofazimine and review of the literature. 290
Melkersson–Rosenthal syndrome: clinical, pathological, and therapeutic considerations. 290
Melkersson–Rosenthal syndrome in childhood: successful management with combination steroid and minocycline therapy. 290
Minocycline in granulomatous cheilitis: experience with 6 cases. 290
Granulomatous cheilitis successfully treated with roxithromycin. 290
Successful treatment of granulomatous cheilitis with roxithromycin. 290
Treatment and follow-up of persistent granulomatous cheilitis with intralesional steroid and metronidazole. 290
Cheilitis granulomatosa treated with metronidazole. 290
Treatment of granulomatous cheilitis with infliximab. 290
Melkersson–Rosenthal syndrome: a form of pseudoangioedema. 290
Successful treatment of granulomatous cheilitis with adalimumab. 290
Third-line therapies 291
Plastic surgical solutions for Melkersson–Rosenthal syndrome: facial liposuction and cheiloplasty procedures. 291
Cheilitis granulomatosa: successful treatment with combined local triamcinolone injections and surgery. 291
Long-term results after surgical reduction cheiloplasty in patients with Melkersson–Rosenthal syndrome and cheilitis granulomatosa. 291
Lip reduction cheiloplasty for Miescher’s granulomatous macrocheilitis (cheilitis granulomatosa) in childhood. 291
Treatment of Miesche’s cheilitis granulomatosa in Melkersson–Rosenthal syndrome. 291
Melkersson–Rosenthal syndrome: reduction cheiloplasty utilizing a transmodiolar labial suspension suture. 291
Successful treatment of granulomatous cheilitis with thalidomide. 291
Cheilitis granulomatosa: report of six cases and review of the literature. 291
95 Hailey–Hailey disease 292
Management strategy 292
Specific investigations 292
First-line therapies 292
Hailey–Hailey disease: the clinical features, response to treatment and prognosis. 292
Second-line therapies 292
Topical tacrolimus ointment is an effective therapy for Hailey–Hailey disease. 292
Is topical tacrolimus really an effective therapy for Hailey–Hailey disease? 292
Treatment of Hailey–Hailey disease with tacrolimus ointment and clobetasol propionate foam. 293
Familial benign chronic pemphigus (Hailey–Hailey disease): use of topical immunomodulators as a modern treatment option. 293
Treatment of Hailey–Hailey disease with topical calcitriol. 293
Generalized Hailey–Hailey disease. 293
Benign familial chronic pemphigus treated with dapsone. 293
Topical cyclosporine in chronic benign familial pemphigus (Hailey–Hailey disease). 293
Benign familial pemphigus responsive to cyclosporine, a possible role for cellular immunity in pathogenesis. 293
Benign familial chronic pemphigus (Hailey–Hailey disease) responds to cyclosporine. 293
Intracutaneous botulinum toxin A versus ablative therapy of Hailey–Hailey disease: a case report. 293
Botulinum toxin type A for the treatment of axillary Hailey–Hailey disease. 293
Botulinum toxin type A as an adjuvant treatment modality for extensive Hailey–Hailey disease. 293
Third-line therapies 293
Surgical eradication of familial benign chronic pemphigus from the axillae. 293
Dermabrasion of Hailey–Hailey disease. 293
Refractory Hailey–Hailey disease successfully treated with sandpaper dermabrasion. 293
Familial benign chronic pemphigus (Hailey–Hailey disease): treatment with carbon dioxide laser vaporization. 293
Effective treatment of Hailey-Hailey disease with a long-pulsed (5 ms) alexandrite laser. 293
Persistent improvement of previously recalcitrant Hailey–Hailey disease with electron beam therapy. 293
Methotrexate for refractory Hailey–Hailey disease. 293
Vesiculobullous Hailey–Hailey disease: successful treatment with oral retinoids. 293
Successful treatment of Hailey–Hailey disease with actitretin. 293
Successful treatment of Hailey–Hailey disease with topical 5-fluorouracil. 293
Case reports of etanercept in inflammatory dermatoses. 293
A case report of Hailey–Hailey disease treated with alefacept (Amevive). 293
Experience with photodynamic therapy in Hailey–Hailey disease. 293
96 Hemangiomas 294
Management strategy 294
Specific investigations 294
Soft-tissue vascular anomalies: utility of US for diagnosis. 294
Hemangioma from head to toe: MR imaging with pathologic correlation. 295
First-line therapies 295
Ultrapotent topical corticosteroid treatment of hemangiomas of infancy. 295
Topical treatment of periocular capillary hemangioma. 295
Intralesional corticosteroid therapy in proliferating head and neck hemangiomas: a review of 155 cases. 295
Oral corticosteroid use is effective for cutaneous hemangiomas. 295
Timolol maleate 0.5% or 0.1% gel-forming solution for infantile hemangiomas: a retrospective, multicenter, cohort study. 295
Propranolol therapy in 55 infants with infantile hemangioma: dosage, duration, adverse effects, and outcome. 295
Second-line therapies 295
Interferon alfa-2a therapy for life-threatening hemangiomas of infancy. 295
Treatment with interferon-alpha 2b in children with life-threatening hemangiomas. 296
Flashlamp-pumped pulsed dye laser for hemangiomas in infancy: treatment of superficial vs. mixed hemangiomas. 296
Surgical treatment of hemangioma in infants. 296
Response of ulcerated perineal hemangiomas of infancy to becaplermin gel, a recombinant human platelet-derived growth factor. 296
Third-line therapies 296
Vincristine as a treatment for a large haemangioma threatening vital functions. 296
Topical imiquimod in the treatment of infantile hemangiomas: a retrospective study. 296
Role of intralesional bleomycin in the treatment of complicated hemangiomas: prospective clinical study. 296
97 Hereditary angioedema 297
Management strategy 297
Acute angioedema 297
Long-term prophylaxis 297
Prevention of relapse due to dental and surgical interventions 297
Specific investigations 297
Angioedema. 297
Hereditary and acquired C1 inhibitor deficiency: biological and clinical characteristics in 235 patients. 298
A multicentre evaluation of the diagnostic efficiency of serological investigations for C1 inhibitor deficiency. 298
Missense mutations in the coagulation factor 12 (Hageman factor) gene in hereditary angioedema with normal C1 inhibition. 298
Acute Angioedema 298
First-line therapies 298
Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patients with hereditary angioedema. 298
Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate. 298
Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy. 298
C1-esterase inhibitor transfusions in patients with hereditary angioedema. 298
Nanofiltered C1 inhibitor concentrate for treatment of hereditary angioedema. 298
Second-line therapies 298
Replacement therapy in hereditary angioedema: successful treatment of two patients with fresh frozen plasma. 298
The safety of fresh frozen plasma for the treatment of hereditary angioedema. 298
Treatment of acute edema attacks in hereditary angioedema with a bradykinin receptor-2 antagonist (icatibant). 299
Icatibant, a new bradykinin receptor antagonist in hereditary angioedema. 299
Home treatment of hereditary angioedema with icatibant administered by health care professionals. 299
Ecallantide for the treatment of acute attacks in hereditary angioedema. 299
Long-term prophylaxis of hereditary angioedema 299
First-line therapies 299
How do we treat patients with hereditary angioedema? 299
Treatment of hereditary angioedema with danazol. 299
Long-term treatment of hereditary angioedema with attenuated androgens: a survey of a 13-year experience. 299
Hereditary angioedema: safety of long-term stanozolol therapy. 299
Side effects of long-term prophylaxis with attenuated androgens in hereditary angioedema: comparison of treated and untreated patients. 299
Second-line therapies 299
Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients. 299
Tranexamic acid therapy in hereditary angioneurotic edema. 299
Epsilon aminocaproic acid therapy of hereditary angioneurotic edema: a double blind study. 300
Long-term treatment of C1 inhibitor deficiency with epsilon aminocaproic acid in two patients. 300
Third-line therapies 300
Long-term prophylaxis with C1 inhibitor (C1 INH) concentrate in patients with recurrent angioedema caused by hereditary and acquired C1 INH deficiency. 300
Pharmacokinetics of pasteurised C1 inhibitor concentrate (Berinert P) in 40 patients with hereditary angioedema. 300
Prevention of relapse due to dental and surgical interventions 300
First-line therapies 300
Hereditary angioedema: the use of fresh frozen plasma for prophylaxis in patients undergoing oral surgery. 300
The efficacy of short-term danazol prophylaxis in hereditary angioedema patients undergoing maxillofacial and dental procedures. 300
Hereditary angioedema: uncomplicated faciomaxillary surgery using short term C1 inhibitor replacement therapy. 300
Tranexamic acid: preoperative prophylactic therapy for patients with hereditary angioneurotic edema. 300
Treatment in children 300
Clinical management of hereditary angio-edema in children. 300
Hereditary angioedema type 3 300
Hereditary angioedema type 3, angioedema associated with angiotensin II receptor antagonists and female sex. 300
98 Hereditary hemorrhagic telangiectasia 301
Management strategy 301
Specific investigations 301
Hereditary hemorrhagic telangiectasia: from molecular biology to patient care. 302
Evidence of small-bowel involvement in hereditary hemorrhagic telangiectasia: a capsule-endoscopic study. 302
Evaluation of patients with hereditary hemorrhagic telangiectasia with video capsule endoscopy: a single-center prospective study. 302
Liver disease in patients with hereditary hemorrhagic telangiectasia. 302
First-line therapies 302
Outcome of septal dermoplasty in patients with hereditary hemorrhagic telangiectasia. 302
Long-term outcome of argon plasma ablation therapy for bleeding in 100 consecutive patients with colonic angiodysplasia. 302
Mucosal vascular malformations of the gastrointestinal tract: clinical observations and results of neodymium: yttrium-aluminum-garnet laser therapy. 302
Diagnosis and management of gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia. 303
Treatment of bleeding gastrointestinal vascular malformations with estrogen-progesterone. 303
Use of estrogen in treatment of familial hemorrhagic telangiectasia. 303
Second-line or temporizing therapies 303
Antiestrogen therapy for hereditary hemorrhagic telangiectasia: a double-blind placebo-controlled clinical trial. 303
Treatment of hereditary hemorrhagic telangiectasia with submucosal and topical bevacizumab therapy. 303
99 Herpes genitalis 304
Management strategy 304
Specific investigations 304
Using the evidence base on genital herpes: optimizing the use of diagnostic tests and information provision. 304
Polymerase chain reaction for detection of herpes simplex virus (HSV) DNA on mucosal surfaces: comparison with HSV isolation in cell culture. 304
Use of glycoprotein G-based type-specific assay to detect antibodies to herpes simplex virus type 2 among persons attending sexually transmitted disease clinics. 304
First-line therapies 304
Primary genital infection 304
Genital herpes. 304
Acute reactivation episodes 305
100 Herpes labialis 308
Management strategy 308
Specific investigations 308
First-line therapies 308
Primary cutaneous infection 308
Treatment of herpes simplex gingivostomatitis with acyclovir in children: a randomized double blind placebo controlled study. 308
Acute reactivation episodes 308
Acyclovir cream for treatment of herpes simplex labialis: results of two randomized, double-blind, vehicle-controlled multicenter clinical trials. 308
Early treatment of cold sores with topical ME-180 decreases the frequency of ulcerative lesions: a randomized, double-blind, placebo-controlled, patient-initiated clinical trial. 309
Treatment of recurrent herpes simplex labialis with oral acyclovir. 309
Second-line therapies 309
Recurrent herpes labialis: efficiacy of topical therapy with penciclovir compared with acyclovir. 309
High-dose, short-duration, early valacyclovir therapy for episodic treatment of cold sores: results of two randomized, placebo-controlled multicenter studies. 309
Single-dose, patient-initiated famciclovir: a randomized, double-blind, placebo-controlled trial for episodic treatment of herpes labialis. 309
Third-line therapies 309
Multicenter collaborative trial of intravenous acyclovir for treatment of mucocutaneous herpes simplex virus infection in the immunocompromised host. 309
Foscarnet treatment of acyclovir-resistant herpes simplex virus infection in patients with acquired immunodeficiency syndrome: preliminary results of a controlled, randomized, regimen-controlled trial. 309
A controlled trial comparing foscarnet with vidarabine for acyclovir-resistant mucocutaneous herpes simplex in the acquired immunodeficiency syndrome. 309
Treatment with intravenous (S)-1-[hydroxy-2-(phosphonylmethoxy)propyl]-cytosine of acyclovir-resistant mucocutaneous infection with herpes simplex virus in a patient with AIDS. 309
A randomized, double-blind, placebo-controlled trial of cidofovir gel for the treatment of acyclovir-unresponsive mucocutaneous herpes simplex virus infection in patients with AIDS. 309
Prophylactic treatment 309
Prevention of ultraviolet-light-induced herpes labialis by sunscreen. 310
Oral acyclovir to suppress frequently recurrent herpes labialis: a double-blind, placebo-controlled trial. 310
Valacyclovir for prevention of recurrent herpes labialis: 2 double-blind, placebo-controlled studies. 310
Valacyclovir prophylaxis for the prevention of herpes simplex virus reactivation in recipients of progenitor cell transplantation. 310
Famciclovir prophylaxis of herpes simplex virus reactivation after laser skin resurfacing. 310
The efficacy of valacyclovir in preventing recurrent herpes simplex virus infections associated with dental procedures. 310
Other therapies 310
Early application of topical 15% idoxuridine in dimethylsulfoxide shortens the course of herpes simplex labialis: a multicenter placebo-controlled trial. 310
Trifluorothymidine 0.5% ointment in the treatment of acyclovir-resistant mucocutaneous herpes simplex in AIDS. 310
Clinical efficay of topical docosanol 10% cream for herpes simplex labialis: a multicenter, randomized, placebo-controlled trial. 310
A randomised double-blind study comparing the effect of 1072-nm light against placebo for the treatment of herpes labialis. 310
101 Herpes zoster 311
Management strategy 311
Specific investigations 311
First-line therapies 311
Valacyclovir compared with acyclovir for improved therapy for herpes zoster in immunocompetent adults. 311
Antiviral therapy for herpes zoster: randomized, controlled clinical trial of valacyclovir and famciclovir therapy in immunocompetent patients 50 years and older. 311
Factors influencing pain outcome in herpes zoster: an observational study with valacyclovir. 311
Famciclovir for the treatment of acute herpes zoster: effects on acute disease and postherpetic neuralgia. A randomized, double-blind, placebo controlled trial. 311
Double-blind, randomized, acyclovir-controlled, parallel-group trial comparing the safety and efficacy of famciclovir and acyclovir in patients with uncomplicated herpes zoster. 312
Oral acyclovir therapy accelerates pain resolution in patients with herpes zoster: a meta-analysis of placebo-controlled trials. 312
Antiviral treatment for preventing postherpetic neuralgia. 312
Second-line therapies 312
Pregabalin for the treatment of postherpetic neuralgia: a randomized, placebo-controlled trial. 312
Pregabalin and transcutaneous electrical nerve stimulation for postherpetic neuralgia treatment. 312
Gabapentin for the treatment of post-herpetic neuralgia: a randomized controlled trial. 312
Incidence of postherpetic neuralgia after combination treatment with gabapentin and valacyclovir in patients with acute herpes zoster: open-label study. 312
Gabapentin versus nortriptyline in post-herpetic neuralgia patients: a randomized, double blind clinical trial: The GONIP Trial. 312
Nortriptyline versus amitriptyline in post-herpetic neuralgia: a randomized trial. 312
The effects of pre-emptive treatment of postherpetic neuralgia with amitriptyline: a randomized, double-blind, placebo-controlled trial. 313
Topical lidocaine for the treatment of postherpetic neuralgia. 313
Efficacy of oxycodone in neuropathic pain: a randomized trial in post-herpetic neuralgia. 313
Third-line therapies 313
A vaccine to prevent herpes zoster and postherpetic neuralgia in older adults. 313
Efficacy, safety, and tolerability of herpes zoster vaccine in persons aged 50–59 years. 313
Acyclovir with and without prednisone for the treatment of herpes zoster. A randomized placebo-controlled trial. 313
A randomized trial of acyclovir for 7 days or 21 days with and without prednisolone for treatment of acute herpes zoster. 313
Contacts with varicella or with children and protection against herpes zoster in adults: a case controlled study. 313
A randomized vehicle-controlled trial of topical capsaicin in the treatment of postherpetic neuralgia. 313
Benzydamine cream for the treatment of post-herpetic neuralgia: minimum duration of treatment periods in a cross-over trial. 313
Tramadol in post-herpetic neuralgia: a randomized, double-blind, placebo-controlled trial. 313
Neuraxial and sympathetic blocks in herpes zoster and postherpetic neuralgia: an appraisal of current evidence. 313
Modified Jaipur block for the treatment of post- herpetic neuralgia. 313
Transcutaneous electrical nerve stimulation for chronic pain. 313
Cryoanalgesia for post-herpetic neuralgia: a new treatment. 313
102 Hidradenitis suppurativa 314
Management strategy 314
Specific investigations 314
Hidradenitis suppurativa: disease of follicular epithelium rather than disease of apocrine glands. 314
First-line therapies 314
Topical treatment of hidradenitis suppurativa with clindamycin. 314
A randomised trial of topical clindamycin vs. systemic tetracycline in hidradenitis suppurativa with special reference to disease assessment. 315
Extent of surgery and recurrence rate of hidradenitis suppurativa. 315
Second-line therapies 315
Combination therapy with clindamycin and rifampicin for hidradenitis suppurativa: a series of 116 consecutive patients. 315
Long-term results of acitretin therapy for hidradenitis suppurativa. Is acne inversa also a misnomer? 315
Third-line therapies 315
Adalimumab for the treatment of moderate to severe Hidradenitis suppurativa: a parallel randomized trial. 315
A double-blind placebo-controlled randomized trial of adalimumab in the treatment of hidradenitis suppurativa. 315
Infliximab therapy for patients with moderate to severe hidradenitis suppurativa: a randomized, double-blind, placebo-controlled crossover trial. 315
Dapsone therapy for hidradenitis suppurativa: a series of 24 patients. 315
Cyclosporine-responsive hidradenitis suppurativa. 315
103 Histoplasmosis 316
Management strategy 316
Specific investigations 316
First-line therapies 317
Disseminated histoplasmosis in patients with AIDS in Panama: a review of 104 cases. 317
Safety and efficacy of liposomal amphotericin B compared with conventional amphotericin B for induction therapy of histoplasmosis in patients with AIDS. 317
Itraconazole therapy for blastomycosis and histoplasmosis. 317
Itraconazole treatment of disseminated histoplasmosis in patients with the acquired immunodeficiency syndrome. 317
Safety of discontinuation of maintenance therapy for disseminated histoplasmosis after immunologic response to anti retroviral therapy. 317
Literature review and case histories of Histoplasma capsulatum var. duboisii infections in HIV-infected patients. 317
Second-line therapies 317
Treatment of blastomycosis and histoplasmosis with ketoconazole. Results of a prospective randomized clinical trial. 317
Fluconazole therapy for histoplasmosis. 317
Treatment of histoplasmosis with fluconazole in patients with acquired immunodeficiency syndrome. 318
Salvage treatment of histoplasmosis with posaconazole. 318
Voriconazole use for endemic fungal infections. 318
Clinical practice guidelines for the management of patients with histoplasmosis: 2007 update by the Infectious Diseases Society of America. 318
Mild acute pulmonary histoplasmosis 318
Severe acute pulmonary histoplasmosis 318
Chronic cavitary pulmonary histoplasmosis 318
Mild disseminated histoplasmosis 318
Severe disseminated histoplasmosis 318
CNS histoplasmosis 318
Treatment of histoplasmosis in pregnancy 318
An official American Thoracic Society statement. Treatment of fungal infections in adult pulmonary and critical care patients. 318
104 Hydroa vacciniforme 319
Management strategy 319
Specific investigations 319
Hydroa vacciniforme–Aktionsspektrum. 319
Hydroa vacciniforme: a review of ten cases. 319
105 Hyperhidrosis 322
Management strategy 322
Specific investigations 323
First-line therapies 323
Aluminium chloride hexahydrate versus palmar hyperhidrosis. Evaporimeter study. 323
Axillary hyperhidrosis. Local treatment with aluminium-chloride hexahydrate 25% in absolute ethanol with and without supplementary treatment with triethanolamine. 323
Second-line therapies 323
Topical glycopyrrolate for patients with facial hyperhidrosis. 323
The use of topical glycopyrrolate in the treatment of hyperhidrosis. 324
Propantheline bromide in the management of hyperhidrosis associated with spinal cord injury. 324
Use of oral glycopyrronium bromide in hyperhidrosis. 324
Systemic therapy for primary hyperhidrosis: a retrospective study of 59 patients treated with glycopyrrolate or clonidine. 324
A randomized placebo-controlled trial of oxybutinin for the initial treatment of palmar and axillary hyperhidrosis. 324
Iontophoresis with alternating current and direct current offset (AC/DC iontophoresis): a new approach for the treatment of hyperhidrosis. 324
Treatment of hyperhidrosis by a battery operated iontopheretic device. 324
Treatment of hyperhidrosis. 324
Botulinum toxin A for axillary hyperhidrosis (excessive sweating). 324
Botulinum toxin therapy for palmar hyperhidrosis. 324
Double-blind trial of botulinum A toxin for the treatment of focal hyperhidrosis of the palms. 324
A double-blind, randomized, comparative study of Dysport™ vs. Botox™ in primary palmar hyperhidrosis. 324
Effective treatment of frontal hyperhidrosis with botulinum toxin A. 324
Treatment of plantar hyperhidrosis with botulinum toxin type A. 324
BOTOX™ delivery by iontophoresis. 324
Botulinum toxin type B: a new therapy for axillary hyperhidrosis. 324
Liposuction for the treatment of axillary hyperhidrosis. 325
Surgical treatment of axillary hyperhidrosis in 123 patients. 325
Endoscopic thoracic sympathectomy for primary hyperhidrosis of the upper limbs: a critical analysis and longterm results of 480 operations. 325
Transthoracic endoscopic sympathectomy for palmar hyperhidrosis in children and adolescents: analysis of 350 cases. 325
Thoracoscopic sympathectomy for disabling palmar hyperhidrosis: a prospective randomized comparison between two levels. 325
Third-line therapies 325
Clinical evaluation of a microwave based device for treating axillary hyperhirosis. 325
Use of biofeedback in treating chronic hyperhidrosis. 325
Emotional eccrine sweating. A heritable disorder. 325
Unilateral localized hyperhidrosis responding to treatment with clonazepam. 325
Clonidine treatment in paroxysmal localized hyperhidrosis. 325
106 Hypertrichosis and hirsutism 326
Management strategy 326
Specific investigations 327
The evaluation and treatment of androgen excess. 327
The clinical evaluation of hirsutism. 327
First-line therapies 327
Consensus on women’s health aspects of polycystic ovarian syndrome (PCOS): the Amsterdam ESHRE/ASRM-Sponsored 3rd PCOS Consensus Workshop Group. 327
Factors affecting the degree of hirsutism in patients with polycystic ovarian syndrome. 327
Hirsutism. 327
Medical treatments of hirsutism. 327
A comparative study of axillary hair removal in women: plucking versus the blend method. 327
Evidence based review of hair removal using lasers and light sources. 327
Meta-analysis of hair removal laser trials. 327
Comparison of long-pulsed alexandrite and Nd : YAG lasers, individually and in combination, for leg hair reduction: an assessor blinded, randomized trial with 18 months of follow-up. 328
Randomized, double blind clinical evaluation of the efficacy and safety of topical eflornithine HCl 13.9% cream in the treatment of women with facial hair. 328
A randomized bilateral vehicle controlled study of eflornithine cream combined with laser treatment versus laser treatment alone for facial hirsutism in women. 328
Second-line therapies 328
107 Ichthyoses 329
Management strategy 329
Specific investigations 329
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009. 330
Expanding the keratin mutation database: novel and recurrent mutations and genotype–phenotype correlation in 28 patients with epidermolytic ichthyosis. 330
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots ALOXE3 and allelic heterogeneity in ALOX12B. 330
Clinical expression and new SPINK5 splicing defects in Netherton syndrome: unmasking a frequent founder synonymous mutation and unconventional intronic mutations. 330
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema. 330
Vitamin D deficiency and rickets in children and adolescents with ichthyosiform erythroderma in type IV and V skin. 330
Acquired ichthyosis. 330
First-line therapies 330
Association of glycerol and paraffin in the treatment of ichthyosis in children: an international, multicentric, randomized, controlled, double-blind study. 330
Role of topical emollients and moisturizers in the treatment of dry skin barrier disorders. 330
Second-line therapies 330
Efficacy of urea therapy in children with ichthyosis. A multicenter randomized, placebo-controlled, double-blind, semilateral study. 330
Propylene glycol with occlusion for treatment of ichthyosis. 331
Treatment of ichthyosiform diseases with topically applied tazarotene: risk of systemic absorption. 331
Topical liarozole in ichthyosis: a double-blind, left–right comparative study followed by a long-term open maintenance study. 331
Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinization. Results of a randomized, double-blind, vehicle-controlled, right/left comparative study. 331
The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome. 331
Narrowband UVB phototherapy as a novel treatment for Netherton syndrome. 331
Third-line therapies 331
Oral retinoid therapy for disorders of keratinization: single-centre retrospective 25 years’ experience on 23 patients. 331
Oral alitretinoin in congenital ichthyosis: a pilot study shows variable effects and risk of central hypothyroidism. 331
Oral liarozole versus acitretin in the treatment of ichthyosis: a phase II/III multicentre, double-blind, randomized, active-controlled study. 331
Sjögren–Larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 swedish patients. 331
Harlequin ichthyosis: a review of clinical and molecular findings in 45 cases. 331
108 Impetigo 332
Management strategy 332
Specific investigations 332
Interventions for impetigo (Cochrane Review). 332
Impetigo in epidemic and nonepidemic phases: an incidence study over 4½ years in a general population. 333
Impetigo in a population over 8.5 years: incidence, fusidic acid resistance and molecular characteristics. 333
DNA heterogeneity of Staphylococcus aureus strains evaluated by Sma1 and SgrA1 pulsed field gel electrophoresis in patients with impetigo. 333
NVC-422 topical gel for the treatment of impetigo. 333
First-line therapies 333
Interventions for impetigo (Cochrane Review). 333
Treatment of impetigo: oral antibiotics most commonly prescribed. 333
Common skin infections in children. 333
Topical retapamulin ointment, 1%, versus sodium fusidate ointment, 2%, for impetigo: a randomized, observer-blinded, noninferiority study. 333
Topical retapamulin ointment (1% wt/wt) twice daily for 5 days versus oral cephalexin twice daily for 10 days in the treatment of secondarily infected dermatitis: results of a randomized controlled trial. 333
Topical mupirocin treatment of impetigo is equal to oral erythromycin therapy. 333
Impetigo. Current etiology and comparison of penicillin, erythromycin and cephalexin therapies. 333
The frequency of erythromycin-resistant Staphylococcus aureus in impetiginized dermatoses. 334
Second-line therapies 334
Fusidic acid tablets in patients with skin and soft-tissue infection: a dose-finding study. 334
Addition of rifampin to cephalexin therapy for recalcitrant staphylococcal skin infections – an observation. 334
Hydrogen peroxide cream: an alternative to topical antibiotics in the treatment of impetigo contagiosa. 334
Third-line therapies 334
Use of 0.3% triclosan (Bacti-Stat) to eradicate an outbreak of methicillin-resistant Staphylococcus aureus in a neonatal nursery. 334
Prevention and control of nosocomial infection caused by methicillin-resistant Staphylococcus aureus in a premature infant ward: preventive effect of a povidone-iodine wipe of neonatal skin. 334
Treatment of bullous impetigo and the staphylococcal scalded skin syndrome in infants. 334
Effect of handwashing on child health: a randomised controlled trial. 334
109 Irritant contact dermatitis 335
Management strategy 335
Specific investigations 335
Irritant contact dermatitis: a review. 335
Clues to an accurate diagnosis of contact dermatitis. 335
Allergic and irritant contact dermatitis. 335
First-line therapies 335
Current concepts of irritant contact dermatitis. 335
Therapeutic options for chronic hand dermatitis. 336
Effect of glove-occlusion on human skin (II). 336
High-fat petrolatum-based moisturizers and prevention of work-related skin problems in wet-work occupations. 336
A randomized comparison of an emollient containing skin-related lipids with a petrolatum-based emollient as adjunct in the treatment of chronic hand dermatitis. 336
Double-blind, randomized trial of scheduled use of a novel barrier cream and an oil-containing lotion for protecting the hands of health care workers. 336
Clinical efficacy evaluation of a novel barrier protective cream. 336
Do topical corticosteroids modulate skin irritation in human beings? Assessment by transepidermal water loss and visual scoring. 336
Short-term glucocorticoid treatment compromises both permeability barrier homeostasis and stratum corneum integrity: inhibition of epidermal lipid synthesis accounts for functional abnormalities. 336
An open-label pilot study to evaluate the safety and efficacy of topically applied tacrolimus ointment for the treatment of hand and/or foot eczema. 336
Pimecrolimus cream 1%: a potential new treatment for chronic hand dermatitis. 336
Second-line therapies 336
Novel treatment of chronic severe hand dermatitis with bexarotene gel. 336
Comparison of cyclosporine and topical betamethasone 17,21-dipropionate in the treatment of severe chronic hand eczema. 337
PUVA-gel vs. PUVA-bath therapy for severe recalcitrant palmoplantar dermatoses. A randomized, single-blinded prospective study. 337
Local narrowband UVB phototherapy vs. local PUVA in the treatment of chronic hand eczema. 337
Third-line therapies 337
Oral alitretinoin (9-cis-retinoic acid) therapy for chronic hand dermatitis in patients refractory to standard therapy: results of a randomized, double-blind, placebo-controlled, multicenter trial. 337
Alitretinoin: its use in intractable hand eczema and other potential indications. 337
Efficacy and patient perception of Grenz ray therapy in the treatment of dermatoses refractory to other medical therapy. 337
Grenz ray therapy in the new millennium: still a valid treatment option? 337
110 Jellyfish stings 338
Clinical features 338
Major box jellyfish (Chironex fleckeri) 338
Irukandji jellyfish (Carukia barnesi) 338
Bluebottles or Portuguese man-of-war (Physalia species) 338
True jellyfish (Schyphozoans) 338
Seabather’s eruption 338
Cutaneous manifestations of jellyfish stings 338
MANAGEMENT STRATEGY 339
First-line therapies 339
Marine envenomations. Part 1 – Jellyfish. 339
Tropical Australian Stinger Research Unit (TASRU), Cairns. 339
A randomized, controlled field trial for the prevention of jellyfish stings with a topical sting inhibitor. 339
Efficacy of a jellyfish sting inhibitor in preventing jellyfish stings in normal volunteers. 339
Evidence-based treatment of jellyfish stings in North America and Hawaii. 339
Evaluation of the effects of various chemicals on discharge of and pain caused by jellyfish nematocysts. 339
A randomised controlled trial of hot water (45 degrees C) immersion versus ice packs for pain relief in bluebottle stings. 339
First aid treatment of jellyfish stings in Australia. Response to a newly differentiated species. 339
First aid for jellyfish stings: do we really know what we are doing? 339
Is there a role for the use of pressure immobilization bandages in the treatment of jellyfish envenomation in Australia? 339
Antivenom efficacy or effectiveness: the Australian experience. 339
Australian venomous jellyfish, envenomation syndromes, toxins and therapy. 340
Second-line therapies 340
Seabather’s eruption: a case of Caribbean itch. 340
Clinical perspectives on seabather’s eruption, also known as ‘sea lice’. 340
Recurrent dermatitis after solitary envenomation by jellyfish partially responded to tacrolimus ointment 0.1%. 340
Successful management of a delayed and persistent cutaneous reaction to jellyfish with pimecrolimus. 340
Delayed cutaneous reaction to jellyfish. 340
Granulomatous jellyfish dermatitis. 340
Treatment of a pigmented lesion induced by a Pelagia noctiluca sting. 340
111 Jessner’s lymphocytic infiltrate 341
Management strategy 341
Specific investigations 341
The heterogeneity of Jessner’s lymphocytic infiltration of the skin. Immunohistochemical studies suggesting one form of perivascular lymphocytoma. 341
Could Jessner’s lymphocytic infiltrate of the skin be a dermal variant of lupus erythematosus? An analysis of 210 cases. 341
112 Juvenile plantar dermatosis 343
Management strategy 343
Specific investigations 343
Juvenile plantar dermatosis: a new entity. 343
Common pediatric foot dermatoses. 343
Sole dermatitis in children: patch testing revisited. 343
First-line therapies 343
Juvenile plantar dermatosis – an 8 year follow-up of 102 patients. 343
Second-line therapies 343
Juvenile plantar dermatosis. Can sweat cause foot rash and peeling? 343
113 Juvenile xanthogranuloma 345
Management strategy 345
Eye involvement 345
Systemic JXG 345
Triple association of JXG, NF-1, and JMML 345
Association of JXG and hematologic malignancy in adults 345
Specific investigations 345
Radiological and clinicopathological features of orbital xanthogranuloma. 345
Juvenile xanthogranuloma associated with neurofibromatosis-1: 14 patients without evidence of hematologic malignancies. 346
JXG, NF-1 and JMML: alphabet soup or a clinical issue? 346
Juvenile xanthogranuloma in a child with previously unsuspected NF1 and JMML. 346
Concurrent development of eruptive xanthogranulomas and hematologic malignancy: two case reports. 346
First-line therapies 346
Juvenile xanthogranuloma: forms of systemic disease and their clinical implications. 346
Update on juvenile xanthogranuloma: unusual cutaneous and systemic variants. 346
Juvenile xanthogranuloma of the oral mucosa. 346
Second-line therapies 346
Early treatment of juvenile xanthogranuloma of the iris with subconjunctival steroids. 346
Severe congenital systemic juvenile xanthogranuloma in monozygotic twins. 346
Infiltrative subcutaneous juvenile xanthogranuloma of the eyelid in a neonate. 346
Juvenile xanthogranuloma of the corneoscleral limbus. 346
Multiple juvenile xanthogranulomas successfully treated with CO2 laser. 346
Third-line therapies 346
Juvenile xanthogranuloma of the iris in an adult. 346
Treatment of severe disseminated juvenile systemic xanthogranuloma with multiple lesions in the CNS. 346
Prolonged severe pancytopenia preceding the cutaneous lesions of JXG. 346
Successful therapy of systemic JXG in a child. 347
Treatment of JXG. 347
Subdural effusion in a CNS involvement of systemic juvenile xanthogranuloma: a case report treated with vinblastin. 347
Successful treatment of central nervous system juvenile xanthogranulomatosis with cladribine. 347
Juvenile xanthogranuloma with bilateral ocular involvement: complete response after treatment with vinblastine: case report. 347
Juvenile xanthogranuloma with hematological dysfunction treated with 2-chlorodeoxyadenosine (2-CdA) and cytosine arabinoside (AraC). 347
Severe persistent bone marrow failure following therapy with 2-chlorodeoxyadenosine (2-CdA) for relapsing juvenile xanthogranuloma of the brain. 347
A rare case of neonatal systemic xanthogranulomatosis with severe hepatic disease and metachronous skin involvement. 347
114 Kaposi sarcoma 348
Management strategy 348
Specific investigations 348
Management of AIDS-related Kaposi’s sarcoma. 348
Update on KSHV epidemiology, Kaposi sarcoma pathogenesis, and treatment of Kaposi sarcoma. 348
First-line therapies 348
PEGylated liposomal doxorubicin plus highly active antiretroviral therapy versus highly active antiretroviral therapy alone in HIV patients with Kaposi’s sarcoma. 348
A randomized controlled trial of highly active antiretroviral therapy versus highly active antiretroviral therapy and chemotherapy in therapy-naive patients with HIV-associated Kaposi sarcoma in South Africa. 348
Multicenter trial of low-dose paclitaxel in patients with advanced AIDS-related Kaposi sarcoma. 348
Randomized trial of paclitaxel versus pegylated liposomal doxorubicin for advanced human immunodeficiency virus-associated Kaposi sarcoma. 349
Highly active antiretroviral therapy in AIDS-associated Kaposi’s sarcoma: implications for the design of therapeutic trials in patients with advanced, symptomatic Kaposi’s sarcoma. 349
Cryotherapy for cutaneous Kaposi’s sarcoma (KS) associated with acquired immune deficiency syndrome (AIDS): a phase II trial. 349
Radiotherapy of classic and human immunodeficiency virus-related Kaposi’s sarcoma: results in 1482 lesions. 349
Phase III vehicle-controlled, multi-centered study of topical alitretinoin gel 0.1% in cutaneous AIDS-related Kaposi’s sarcoma. 349
Second-line therapies 349
Intralesional interferon-alpha and zidovudine in epidemic Kaposi’s sarcoma. 349
Interferon-alpha2b with protease inhibitor-based antiretroviral therapy in patients with AIDS-associated Kaposi sarcoma: an AIDS malignancy consortium phase I trial. 349
Intralesional vinblastine for cutaneous Kaposi’s sarcoma associated with acquired immunodeficiency syndrome. 349
Third-line therapies 349
Phase II study of bevacizumab in patients with HIV-associated Kaposi’s sarcoma receiving antiretroviral therapy. 349
A Kaposi’s sarcoma complete clinical response after sorafenib administration. 349
Lenalidomide in treating AIDS-related Kaposi’s sarcoma. 349
A retrospective analysis of thalidomide therapy in non-HIV-related Kaposi’s sarcoma. 349
A multicenter phase II study of the intravenous administration of liposomal tretinoin in patients with acquired immunodeficiency syndrome-associated Kaposi’s sarcoma. 350
New photodynamic therapy protocol to treat AIDS-related Kaposi’s sarcoma. 350
9-cis-retinoic acid capsules in the treatment of AIDS-related Kaposi sarcoma: results of a phase 2 multicenter clinical trial. 350
Phase II evaluation of low-dose oral etoposide for the treatment of relapsed or progressive AIDS-related Kaposi’s sarcoma: an AIDS Clinical Trials Group clinical study. 350
Sirolimus for Kaposi’s sarcoma in renal-transplant recipients. 350
Rapamycin with antiretroviral therapy in AIDS-associated Kaposi sarcoma: an AIDS malignancy consortium study. 350
Phase 2 study of pegylated liposomal doxorubicin in combination with interleukin-12 for AIDS-related Kaposi sarcoma. 350
Activity of subcutaneous interleukin-12 in AIDS-related Kaposi sarcoma. 350
Randomized phase II trial of matrix metalloproteinase inhibitor COL-3 in AIDS-related Kaposi’s sarcoma: an AIDS Malignancy Consortium Study. 350
Phase II AIDS malignancy consortium trial of topical halofuginone in AIDS-related Kaposi’s sarcoma. 350
Imiquimod 5% cream for treatment of HIV-negative Kaposi’s sarcoma skin lesions: a phase I to II, open-label trial in 17 patients. 350
Intralesional vinblastine vs. 3% sodium tetradecyl sulfate for the treatment of oral Kaposi’s sarcoma. A double blind, randomized clinical trial. 350
Local therapy for mucocutaneous Kaposi’s sarcoma in patients with acquired immunodeficiency syndrome. 350
Oral ganciclovir for patients with cytomegalovirus retinitis treated with a ganciclovir implant. 350
Effect of antiviral drugs used to treat cytomegalovirus end-organ disease on subsequent course of previously diagnosed Kaposi’s sarcoma in patients with AIDS. 350
Successful treatment of classical Kaposi sarcoma with low-dose intramuscular immunoglobulins. 350
115 Kawasaki disease 351
Management strategies 351
Specific investigations 351
Kawasaki disease: an overview. 351
The diagnosis and treatment of Kawasaki disease. 351
First-line therapies 351
Kawasaki disease: an update on diagnosis and treatment. 351
Resistance to intravenous immunoglobulin in children with Kawasaki disease. 352
Analysis of potential risk factors associated with nonresponse to initial intravenous immunoglobulin treatment among Kawasaki disease patients in Japan. 352
Treatment of acute Kawasaki disease: aspirin’s role in the febrile stage revisited. 352
Revisit high dose aspirin in acute stage of Kawasaki disease. 352
Second-line therapies 352
Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blinded-endpoints trial. 352
Effects of steroid pulse therapy on immunoglobulin-resistant Kawasaki disease. 352
Risk factors associated with the need for additional intravenous gamma-globulin therapy for Kawasaki disease. 352
Third-line therapies 352
Cyclosporin A treatment for Kawasaki disease refractory to initial and additional intravenous immunoglobulin. 353
Response of refractory Kawasaki disease to pulse steroid and cyclosporin A therapy. 353
Ulinastatin, a urinary trypsin inhibitor, for the initial treatment of patients with Kawasaki disease: a retrospective study. 353
Infliximab for intravenous immunoglobulin resistance in Kawasaki disease: a retrospective study. 353
Resistant Kawasaki disease treated with anti-CD20. 353
Long-term efficacy of plasma exchange treatment for refractory Kawasaki disease. 353
Prevention of thrombosis of coronary aneurysms in patients with a history of Kawasaki disease. 353
Optimal time of surgical treatment for Kawasaki coronary artery disease. 353
116 Keloids 354
Management strategy 354
Specific investigations 354
Dermatofibrosarcoma protuberans is a unique fibrohistiocytic tumour expressing CD34. 354
First-line therapies 354
A new uniform protocol of combined corticosteroid injections and ointment application reduces recurrence rates after surgical keloid/hypertrophic scar excision. 354
Keloids treated with topical injections of triamcinolone acetonide. Immediate and long term results. 355
Outcomes of surgical excision with pressure therapy using magnets and identification of risk factors for recurrent keloids. 355
A surgical approach for earlobe keloid: keloid fillet flap. 355
Comparison of a silicone gel-filled cushion and silicon gel sheeting for the treatment of hypertrophic or keloid scars. 355
Clinical evaluation of a new self-drying silicone gel in the treatment of scars: a preliminary report. 355
Combination of different techniques for the treatment of earlobe keloids. 355
Effects of combined intralesional 5-fluorouracil and topical silicone in prevention of keloids: a double blind randomized clinical trial study. 355
Comparison of the efficacy of intralesional triamcinolone acetonide and 5-fluorouracil tattooing for the treatment of keloids. 355
Second-line therapies 355
Recurrence rates of excised keloids treated with postoperative triamcinolone acetonide injections or interferon alfa-2b injections. 355
Effects of interferon-α2b on keloid treatment with triamcinolone acetonide intralesional injection. 355
Cryotherapy in the treatment of keloids. 355
A comparison of the combined effect of cryotherapy and corticosteroid injections versus corticosteroids and cryotherapy alone on keloids: a controlled study. 355
Treatment of earlobe keloids using the cobalt 60 teletherapy unit. 356
Keloids can be forced into remission with surgical excision and radiation, followed by adjuvant therapy. 356
Treatment of keloids by surgical excision and immediate postoperative single-fraction radiotherapy. 356
The treatment of 783 keloid scars by iridium 192 interstitial irradiation after surgical excision. 356
Retrospective analysis of treatment of unresectable keloids with primary radiation over 25 years. 356
Postoperative high-dose-rate brachytherapy in the prevention of keloids. 356
Post-keloidectomy irradiation using high-dose-rate superficial brachytherapy. 356
Third-line therapies 356
Management of ear lobule keloids using 980-nm diode laser. 356
Effect of pulse width of a 595-nm flashlamp-pumped pulsed dye laser on the treatment response of keloidal and hypertrophic sternotomy scars. 356
The effect of carbon dioxide laser surgery on the recurrence of keloids. 356
Pilot study of the effect of postoperative imiquimod 5% cream on the recurrence rate of excised keloids. 356
Role of mitomycin C in reducing keloid recurrence: patient series and literature review. 356
Intralesional interferon gamma treatment for keloids and hypertrophic scars. 356
The local treatment of hypertrophic scars and keloids with topical retinoic acid. 356
Treatment of keloids and hypertrophic scars using bleomycin. 356
Comparison of intralesional verapamil with intralesional triamcinolone in the treatment of hypertrophic scars and keloids. 357
117 Keratoacanthoma 358
Management strategy 358
Specific investigations 358
Small, solitary keratoacanthoma 358
First-line therapies 358
Evaluation of curettage and electrodesiccation in the treatment of keratoacanthoma. 359
Keratoacanthomas treated with Mohs’ micrographic surgery (chemosurgery). A review of forty-three cases. 359
Keratoacanthoma observed. 359
Second-line therapies 359
Topical treatment with imiquimod may induce regression of facial keratoacanthoma. 359
Spontaneous regression of keratoacanthoma can be promoted by topical treatment with imiquimod cream. 359
Intralesional methotrexate treatment for keratoacanthoma tumours: a retrospective study and review of the literature. 359
Topical 5-fluorouracil as primary therapy for keratoacanthoma. 359
Efficacy of topical photodynamic therapy for keratoacanthomas: a case-series of four patients. 359
Argon laser treatment of small keratoacanthomas in difficult locations. 359
Large, rapidly proliferating keratoacanthoma 359
First-line therapies 359
Treatment of aggressive keratoacanthomas by radiotherapy. 359
Treatment of keratoacanthomas with intralesional fluorouracil. 359
Treatment of keratoacanthomas with intralesional methotrexate. 359
Intralesional methotrexate in solitary keratoacanthoma. 359
Intralesional infusion of methotrexate as neoadjuvant therapy improves the cosmetic and functional results of surgery to treat keratoacanthoma: results of a randomized trial. 359
Intralesional interferon alfa-2b treatment of keratoacanthomas. 360
Use of interferon-alpha (IFN-alpha) in the treatment of keratoacanthoma. 360
Multiple keratoacanthomas 360
118 Keratosis pilaris and variants 361
Management strategy 361
Specific investigations 361
The prevalence of cutaneous manifestations in young patients with type 1 diabetes. 361
Keratosis pilaris: skin marker of Hodgkin’s disease? 362
Keratosis pilaris atrophicans. One heterogeneous disease or a symptom in different clinical entities? 362
First-line therapies 362
Evaluation of a sodium lactate and urea crème to ameliorate keratosis pilaris. 362
Polyester sponge adjunct in acne management. 362
Practical management of widespread, atypical keratosis pilaris. 362
Keratosis pilaris decalvans non-atrophicans. 362
Second-line therapies 362
A comparative trial comparing the efficacy of tacrolimus 0.1% ointment with Aquaphor ointment for the treatment of keratosis pilaris. 362
Tazarotene 0.05% cream for the treatment of keratosis pilaris. 362
Natural history of keratosis pilaris. 362
Clinical findings, cutaneous pathology, and response to therapy in 21 patients with keratosis pilaris atrophicans. 362
A case of atrophoderma vermiculatum responding to isotretinoin. 362
Atrophoderma vermiculatum. Case reports and review. 362
A case of ulerythema ophryogenes responding to isotretinoin. 363
Third-line therapies 363
Keratosis pilaris rubra: a common but underrecognized condition. 363
Natural history of keratosis pilaris. 363
Recalcitrant scarring follicular disorders treated by laser-assisted hair removal: a preliminary report. 363
Folliculitis spinulosa decalvans: successful therapy with dapsone. 363
Treatment of keratosis pilaris atrophicans with the pulsed tunable dye laser. 363
Keratosis rubra pilaris responding to potassium titanyl phosphate laser. 363
Successful treatment of severe keratosis pilaris rubra with a 595-nm pulsed dye laser. 363
Keratosis pilaris rubra and keratosis pilaris atrophicans faciei treated with pulsed dye laser: report of 10 cases. 363
Long-pulsed 1064-nm Nd:YAG laser significantly improves keratosis pilaris: a randomized, evaluator-blind study. 363
119 Langerhans cell histiocytosis 364
Management strategy 364
Specific investigations 364
Histiocytosis syndromes in children: approach to the clinical and laboratory evaluation of children with Langerhans cell histiocytosis. 365
First-line therapies 365
Topical nitrogen mustard: an effective treatment for cutaneous Langerhans cell histiocytosis. 365
Long term follow up of topical mustine treatment for cutaneous Langerhans cell histiocytosis. 365
Topical nitrogen mustard ointment with occlusion for Langerhans’ cell histiocytosis of the scalp. 365
Topical nitrogen mustard in patients with Langerhans cell histiocytosis. 365
Satisfactory remission achieved by PUVA therapy in Langerhans cell histiocytosis in an elderly patient. 365
Cutaneous Langerhans cell histiocytosis in an elderly man successfully treated with narrowband ultraviolet B. 365
Etoposide in recurrent childhood Langerhans cell histiocytosis: an Italian cooperative study. 365
Langerhans cell histiocytosis in childhood: results from the Italian Cooperative AIEOP-CNR-H.X. ‘83 study. 365
A randomised trial of treatment for multisystem Langerhans’ cell histiocytosis. 365
Second-line therapies 365
Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification. 365
Treatment strategy for disseminated Langerhans cell histiocytosis. 366
A case of adult Langerhans cell histiocytosis showing successfully regenerated osseous tissue of the skull after chemotherapy. 366
Successful treatment of cutaneous Langerhans cell histiocytosis with thalidomide. 366
Langerhans cell histiocytosis with vulvar involvement and responding to thalidomide therapy – case report. 366
A phase II trial using thalidomide for Langerhans cell histiocytosis. 366
Oral methotrexate and alternate-day prednisone for low-risk Langerhans cell histiocytosis. 366
Cytosine-arabinoside, vincristine, and prednisolone in the treatment of children with disseminated Langerhans cell histiocytosis with organ dysfunction: experience at a single institution. 366
Successful treatment of Langerhans cell histiocytosis with 2-chlorodeoxyadenosine. 366
Efficacy of continuous infusion 2-CDA (cladribine) in pediatric patients with Langerhans cell histiocytosis. 366
Cladribine (2-chlorodeoxyadenosine) in frontline chemotherapy for adult Langerhans cell histiocytosis: a single centre study of seven cases. 366
Third-line therapies 366
Results of treatment of 127 patients with systemic histiocytosis (Letterer-Siwe syndrome, Schüller-Christian syndrome, and multifocal eosinophilic granuloma). 367
Cyclosporin A therapy for multisystem Langerhans cell histiocytosis. 367
Hematopoietic stem cell transplantation in patients with severe Langerhans cell histiocytosis and hematological dysfunction: experience of the French Langerhans Cell Study Group. 367
Improved outcome of treatment resistant high risk Langerhans cell histiocytosis after allogenic stem cell transplantation with reduced-intensity conditioning. 367
Effect of trimethoprim-sulphamethoxazole in Langerhans cell histiocytosis: preliminary observations. 367
Widespread skin-limited Langerhans cell histiocytosis: complete remission with interferon alpha. 367
Successful treatment of two children with Langerhans’ cell histiocytosis with 2’-deoxycoformycin. 367
Interleukin-2 therapy of Langerhans cell histiocytosis. 367
Langerhans cell histiocytosis: complete remission after oral isotretinoin therapy. 367
Langerhans cell histiocytosis in an adult: good response of cutaneous lesions to acitretin. 367
Lenalidomide induced therapeutic response in a patient with aggressive multi-system Langerhans cell histiocytosis resistant to 2-chlorodeoxyadenosine and early relapse after high dose BEAM chemotherapy with autologous peripheral stem cell transplant. 367
Photodynamic therapy for multi-resistant cutaneous Langerhans cell histiocytosis. 368
Clofarabine in refractory Langerhans cell histiocytosis. 368
Response to subcutaneous therapy with mistletoe in recurrent multisystem Langerhans cell histiocytosis. 368
Future therapeutic approaches 368
Recurrent BRAF mutations in Langerhans cell histiocytosis. 368
120 Leg ulcers 369
Management strategy 369
Wound care 369
Dressing 369
Venous leg ulcers 369
Arterial ulcers 369
Diabetic neuropathy 369
Pressure ulcers 369
First-line therapy 369
Compression for venous leg ulcers. 370
Antibiotics and antiseptics for venous leg ulcers. 370
Management of ischemic heel ulceration and gangrene: an evaluation of factors associated with successful healing. 370
Second-line therapy 370
The impact of ablation of incompetent superficial and perforator veins on ulcer healing rates. 370
A factorial, randomized trial of pentoxifylline or placebo, four-layer or single-layer compression, and knitted viscose or hydrocolloid dressings for venous ulcers. 370
The effectiveness of footwear and offloading interventions to prevent and heal foot ulcers and reduce plantar pressure in diabetes. 370
Contemporary management of diabetic neuropathic foot ulceration: a study of 917 consecutively treated limbs. 370
Third-line therapy 370
Hyperbaric oxygen therapy for chronic wounds. 370
121 Leiomyoma 371
Management strategy 371
Specific investigations 371
Cutaneous smooth muscle neoplasms: clinical features, histological findings and treatment options. 371
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. 371
Evidence for a new fumarate hydratase gene mutation in a unilateral type 2 segmental leiomyomatosis. 371
First-line therapy 371
Leiomyomas of the skin. 372
Second-line therapies 372
Successful treatment of pain in two patients with cutaneous leiomyomata with the oral alpha-1 adrenoceptor antagonist, doxazosin. 372
Pharmacological modulation of cold-induced pain in cutaneous leiomyomata. 372
Multiple cutaneous leiomyomata and erythrocytosis with demonstration of erythropoietic activity in the cutaneous leiomyomata. 372
Therapy for painful cutaneous leiomyomas. 372
Muscle relaxing agent in cutaneous leiomyoma. 372
Leiomyomatosis cutis et uteri. 372
Gabapentin treatment of multiple piloleiomyoma-related pain. 372
Successful pain relief of cutaneous leiomyomata due to Reed syndrome with the combination treatment of pregabalin and duloxetine. 372
A new indication of botulinum toxin: leiomyoma-related pain. 372
Botulinum toxin type A: treatment of a patient with multiple cutaneous piloleiomyomas. 372
Treatment of multiple cutaneous leiomyomas with CO2 laser ablation. 372
122 Leishmaniasis 373
Many faces of cutaneous leishmaniasis. 373
Cutaneous leishmaniasis mimicking inflammatory and neoplastic processes: a clinical, histopathological and molecular study of 57 cases. 373
Management strategy 373
Specific investigations 373
Epidemic of cutaneous leishmaniasis: 109 cases in a population of 500. 374
Genus-specific kinetoplast-DNA PCR and parasite culture for the diagnosis of localized cutaneous leishmaniasis: applications for clinical trials under field conditions in Brazil. 374
Sensitivity of leishmanin skin test in patients of acute cutaneous leishmaniasis. 374
Enzyme-linked immunosorbent assay based on soluble promastigote antigen detects immunoglobulin M (IgM) and IgG antibodies in sera from cases of visceral and cutaneous leishmaniasis. 374
First-line therapies 374
Clinical features, epidemiology, and efficacy and safety of intralesional antimony treatment of cutaneous leishmaniasis: recent experience in Turkey. 374
Clinical efficacy of intramuscular meglumine antimoniate alone and in combination with intralesional meglumine antimoniate in the treatment of Old World cutaneous leishmaniasis. 374
Comparative efficacy of intralesional sodium stibogluconate (SSG) alone and its combination with intramuscular SSG to treat localized cutaneous leishmaniasis: results of a pilot study. 374
Second-line therapies 374
Recurrent American cutaneous leishmaniasis. 374
The role of rifampicin in the management of cutaneous leishmaniasis. 374
Fluconazole for the treatment of cutaneous leishmaniasis caused by Leishmania major. 374
Comparison of oral itraconazole and intramuscular meglumine antimoniate in the treatment of cutaneous leishmaniasis. 375
Intralesional sodium stibogluconate alone or its combination with either intramuscular sodium stibogluconate or oral ketoconazole in the treatment of localized cutaneous leishmaniasis: a comparative study. 375
Efficacy of a weekly cryotherapy regimen to treat Leishmania major cutaneous leishmaniasis. 375
Evaluation of thermotherapy for the treatment of cutaneous leishmaniasis in Kabul, Afghanistan: a randomized controlled trial. 375
Randomized, double-blind, comparative clinical trial on the efficacy and safety of intralesional sodium stibogluconate and intralesional 7% hypertonic sodium chloride against cutaneous leishmaniasis caused by L. donovani. 375
Doxycycline for the treatment of cutaneous leishmaniasis. 375
Third-line therapies 375
Miltefosine in the treatment of cutaneous leishmaniasis caused by Leishmania braziliensis in Brazil: a randomized and controlled trial. 375
Role of imiquimod and parenteral meglumine antimoniate in the initial treatment of cutaneous leishmaniasis. 375
Comparison of topical paromomycin sulfate (twice/day) with intralesional meglumine antimoniate for the treatment of cutaneous leishmaniasis caused by L. major. 375
Comparison between the efficacy of photodynamic therapy and topical paromomycin in the treatment of Old World cutaneous leishmaniasis: a placebo-controlled, randomized clinical trial. 375
The parasiticidal effect of electricity on Leishmania major, both in vitro and in vivo. 375
Evaluation of CO2 laser efficacy in the treatment of cutaneous leishmaniasis. 376
Comparison of intralesionally injected zinc sulfate with meglumine antimoniate in the treatment of acute cutaneous leishmaniasis. 376
Effect of combination therapy with systemic glucantime and pentoxifylline in the treatment of cutaneous leishmaniasis. 376
Liposomal amphotericin B treatment of cutaneous leishmaniasis due to Leishmania tropica. 376
123 Lentigo maligna 377
Management strategy 377
Specific Investigations 377
124 Leprosy (including reactions) 381
Management strategy 381
Specific investigations 382
First-line therapies 382
Leprosy. 382
Treatment of leprosy/Hansen’s disease in the early 21st century. 382
Leprosy: forgotten, but not gone (yet). 382
Human immunodeficiency virus and leprosy: an update. 382
Leprosy and HIV co-infection: a critical approach. 382
The role of thalidomide in the management of erythema nodosum leprosum. 382
Secondary leprosy infection in a patient with psoriasis during treatment with infliximab. 382
Leprosy reaction manifesting after discontinuation of adalimumab therapy. 382
Second-line therapies 382
Response to cyclosporine treatment in Ethiopian and Nepali patients with severe leprosy type 1 reactions. 382
Cyclosporin A treatment of leprosy patients with chronic neuritis is associated with pain control and reduction in antibodies against nerve growth factor. 382
Methotrexate treatment for type 1 (reversal) leprosy reactions. 382
Methotrexate in resistant ENL. 382
Azathioprine as a steroid sparing agent in leprosy type 2 reactions: report of nine cases. 382
Clinical outcomes in a randomized controlled study comparing azathioprine and prednisolone versus prednisolone alone in the treatment of severe leprosy type 1 reactions in Nepal. 382
Type 1 leprosy reversal reaction treated with topical tacrolimus along with systemic corticosteroids. 383
Severe refractory erythema nodosum leprosum successfully treated with the tumor necrosis factor inhibitor etanercept. 383
Treatment of recurrent erythema nodosum leprosum with infliximab. 383
125 Leukocytoclastic vasculitis 384
Management strategy 384
Specific investigations 384
Cutaneous vasculitis in children and adults: associated diseases and etiologic factors in 303 patients. 385
Cutaneous vasculitis update: classification, epidemiology, etiology, pathogenesis, evaluation and prognosis. 385
Clinical approaches to cutaneous vasculitis. 385
First-line therapies 385
Colchicine in the treatment of cutaneous leukocytoclastic vasculitis: results of a prospective, randomized controlled trial. 385
Colchicine is effective in controlling chronic cutaneous leukocytoclastic vasculitis. 385
Dapsone therapy for Henoch–Schönlein purpura: a case series. 385
Dapsone in Henoch–Schönlein purpura. 385
The therapeutic response of urticarial vasculitis to indomethacin. 385
Second-line therapies 385
Early prednisone therapy in Henoch–Schönlein purpura: a randomized, double-blind, placebo-controlled trial. 385
The clinical and histopathologic spectrums of urticarial vasculitis: study of forty cases. 385
Azathioprine. An effective, corticosteroid-sparing therapy for patients with recalcitrant cutaneous lupus erythematosus or with recalcitrant cutaneous leukocytoclastic vasculitis. 385
Prednisone plus azathioprine treatment in patients with rheumatoid arthritis complicated by vasculitis. 386
Methotrexate in patients with moderate systemic lupus erythematosus (exclusion of renal and central nervous system disease). 386
Cyclosporin A in the treatment of cutaneous vasculitis. Clinical and cellular effects. 386
Treatment of complicated Henoch–Schönlein purpura with mycophenolate mofetil: a retrospective case series report. 386
Treatment of severe cutaneous small vessel vasculitis with mycophenolate mofetil. 386
A randomized controlled trial of rituximab following failure of antiviral therapy for hepatitis C-associated cryoglobulinemic vasculitis. 386
A randomized, controlled, trial of rituximab for treatment of severe cryoglobulinemic vasculitis. 386
Management of non-infectious mixed cryoglobulinemia vasculitis: data from 242 cases included in the CryoVas survey. 386
Successful treatment of rheumatoid vasculitis-associated cutaneous ulcers using rituximab in two patients with rheumatoid arthritis. 386
Third-line therapies 386
Elimination diet in the treatment of selected patients with hypersensitivity vasculitis. 386
Leukocytoclastic vasculitis caused by drug additives. 387
Synergistic effects of pentoxifylline and dapsone in leucocytoclastic vasculitis. 387
Chronic leukocytoclastic vasculitis associated with polycythemia vera: effective control with pentoxifylline. 387
Other therapies 387
Plasma exchange in refractory cutaneous vasculitis. 387
Case report: steroid sparing effect of intravenous gamma globulin in a child with necrotizing vasculitis. 387
Successful treatment of chronic leucocytoclastic vasculitis and persistent ulceration with intravenous immunoglobulin. 387
Therapy for severe necrotizing vasculitis with infliximab. 387
Response of deep cutaneous vasculitis to infliximab. 387
Minocycline treatment for leukocytoclastic vasculitis associated with rheumatoid arthritis. 387
Treatment of severe and difficult cases of systemic lupus erythematosus with tacrolimus. A report of three cases. 387
Successful use of interleukin 6 antagonist tocilizumab in a patient with refractory cutaneous lupus and urticarial vasculitis. 387
126 Lichen myxedematosus 388
Management strategy 388
Specific investigations 388
Lichen myxedematosus (papular mucinosis): new concepts and perspectives for an old disease. 388
Lichen myxedematosus associated with chronic hepatitis C. 388
First-line therapies 388
Scleromyxedema. 388
Scleromyxedema: an experience using treatment with systemic corticosteroid and review of the published work. 388
Scleromyxedema: successful treatment of cutaneous and neurologic symptoms. 388
Scleromyxedema: a case series highlighting long-term outcomes of treatment with intravenous immunoglobulin (IVIG). 388
Second-line therapies 389
Generalized papular and sclerodermoid eruption: scleromyxedema. 389
Treatment of recalcitrant scleromyxedema with thalidomide in 3 patients. 389
Discrete papular mucinosis responding to intralesional and topical steroids. 389
Treatment of localized lichen myxedematosus of discrete type with tacrolimus ointment. 389
Third-line therapies 389
Scleromyxedema: role of high-dose melphalan with autologous stem cell transplantation. 389
Response to bortezomib of a patient with scleromyxedema refractory to other therapies. 389
Scleromyxedema with subclinical myositis. 389
Successful treatment of intractable scleromyxedema with cyclosporin A. 389
Arndt Gottron scleromyxedema: successful response to treatment with steroid minipulse and methotrexate. 389
Lichen myxedematosus treated with chlorambucil. 389
Scleromyxedema: treatment with interferon alfa. 389
Cutaneo-systemic papulosclerotic mucinosis (scleromyxedema): remission after extracorporeal photochemotherapy and corticoid bolus. 390
Successful treatment of lichen myxoedematosus with PUVA photochemotherapy. 390
Scleromyxedema: treatment of widespread cutaneous involvement by total skin electron-beam therapy. 390
Vincristine, idarubicin, dexamethasone and thalidomide in scleromyxoedema. 390
127 Lichen nitidus 391
Management strategy 391
Specific investigations 391
First-line therapies 391
Successful treatment of lichen nitidus. 391
Treatment of generalized lichen nitidus with narrow band ultraviolet light. 391
Two cases of generalized lichen nitidus treated successfully with narrow band UVB phototherapy. 391
Second-line therapies 391
Lichen nitidus treated with topical tacrolimus. 391
Generalised lichen nitidus: a report of two cases treated with astemizole. 391
Lichen nitidus treated with astemizole. 391
Treatment of generalized lichen nitidus with PUVA. 391
Association of lichen planus and lichen nitidus – treatment with etretinate. 391
Treatment of palmoplantar lichen nitidus with acitretin. 392
A case of generalized lichen nitidus treated with low dose cyclosporine. 392
Generalized lichen nitidus successfully treated with pimecrolimus 1 percent cream. 392
Third-line therapies 392
Treatment of lichen planus and lichen nitidus with itraconazole: reports of six cases. 392
Improvement of lichen nitidus after topical dinitrochlorobenzene application. 392
Generalised lichen nitidus in a child: response to cetirizine dihydrochloride/levamisol. 392
Generalised lichen nitidus is successfully treated with an antituberculous agent. 392
128 Lichen planopilaris 393
Management strategy 393
Specific investigations 393
A histologic review of 27 patients with lichen planopilaris. 393
Immunofluorescence abnormalities in lichen planopilaris. 393
Dermatoscopy: alternative uses in daily clinical practice. 393
First-line therapies 393
Lichen planopilaris: report of 30 cases and review of the literature. 393
Scarring alopecia. 393
Second-line therapies 393
Postmenopausal frontal fibrosing alopecia: a frontal variant of lichen planopilaris. 394
Lichen planopilaris: clinical and pathologic study of forty-five patients. 394
Oral treatment of keratinizing disorders of skin and mucous membranes with etretinate. Comparative study of 113 patients. 394
A case-series of 29 patients with lichen planopilaris. The Cleveland Clinic Foundation experience on evaluation, diagnosis, and treatment. 394
Hydroxychloroquine and lichen planopilaris: efficacy and introduction of Lichen Planopilaris Activity Index scoring system. 394
Third-line therapies 394
Efficacy and safety of mycophenolate mofetil for lichen planopilaris. 394
Short course of oral cyclosporine in lichen planopilaris. 394
Thalidomide-induced remission of lichen planopilaris. 394
Low-dose excimer 308-nm laser for treatment of lichen planopilaris. 394
Lichen planopilaris treated with a peroxisome proliferator-activated receptor γ-agonist. 394
129 Lichen planus 395
Management strategy 395
Specific investigations 395
Lichen planus and other cutaneous manifestations in chronic hepatitis C: pre- and post-interferon-based treatment prevalence vary in a cohort of patients from low hepatitis C virus endemic area. 395
Drug-induced lichen planus. 395
First-line therapies 395
Betamethasone-17,21-dipropionate ointment: an effective topical preparation in lichen rubra planus. 395
A randomized controlled trial to compare calcipotriol with betamethasone valerate for the treatment of cutaneous lichen planus. 395
Second-line therapies 396
Efficacy of oral metronidazole in treatment of cutaneous and mucosal lichen planus. 396
Efficacy of sulfasalazine in the treatment of generalized lichen planus: randomized double-blinded clinical trial on 52 patients. 396
Treatment of generalized cutaneous lichen planus with dipropionate and betamethasone disodium phosphate: an open study of 73 cases. 396
Treatment of lichen planus with acitretin. A double-blind, placebo-controlled study in 65 patients. 396
Ultraviolet-B treatment for cutaneous lichen planus: our experience with 50 patients. 396
Psoralen plus UVA vs. UVB-311 nm for the treatment of lichen planus. 396
Long-term efficacy of PUVA treatment in lichen planus: comparison of oral and external methoxsalen regimens. 396
Third-line therapies 396
Antimicrobials 397
Treatment of lichen planus with Bactrim. 397
Histopathological evaluation of griseofulvin therapy in lichen planus: a double-blind controlled study. 397
Pulsed itraconazole therapy in eruptive lichen planus. 397
The use of oral terbinafine or topical ciclopirox for lichen planus. 397
Systemic immunosuppressive agents 397
Childhood actinic lichen planus: successful treatment with antimalarials. 397
Successful treatment of resistant hypertrophic and bullous lichen planus with mycophenolate mofetil. 397
Generalized severe lichen planus treated with azathioprine. 397
Palmoplantar lichen planus with umbilicated papules: an atypical case with rapid therapeutic response to cyclosporine. 397
Methotrexate for the treatment of generalized lichen planus. 397
Successful treatment of lichen planus with adalimumab. 397
Nail lichen planus: successful treatment with etanercept. 397
Other 397
Treatment of lichen planus of the penis with photo-dynamic therapy. 397
Successful interferon treatment for lichen planus associated with hepatitis due to hepatitis C virus infection. 398
Lichen planus and chronic hepatitis C: exacerbation of the lichen under interferon therapy. 398
Treatment of cutaneous lichen planus with thalidomide. 398
Ultraviolet A1 in the treatment of generalized lichen planus: a report of 4 cases. 398
Topical tacrolimus in the treatment of lichen planus in a child. 398
Limited benefit of topical calcipotriol in lichen planus treatment: a preliminary study. 398
Use of pimecrolimus cream in disorders other than atopic dermatitis. 398
The successful treatment of palmoplantar hyperkeratotic lichen planus with enoxaparin. 398
Linear lichen planus pigmentosus of the forehead treated by neodymium:yttrium-aluminum-garnet laser and topical tacrolimus. 398
Response of recalcitrant lichen planus to alitretinoin in 3 patients. 398
130 Lichen sclerosus 399
Management strategy 399
Specific investigations 399
Light microscopic criteria for the diagnosis of early vulvar lichen sclerosus: a comparison with lichen planus. 399
A comparative analysis of lichen sclerosus of the vulva and lichen sclerosus that evolves to vulvar squamous cell carcinoma. 399
First-line therapy 399
Topical interventions of genital lichen sclerosus. 400
Clinical and histologic effects of topical treatments of vulval lichen sclerosus. A critical evaluation. 400
The response of balanitis xerotica obliterans to local steroid application compared with placebo in children. 400
Ultrapotent topical corticosteroid treatment of childhood genital lichen sclerosus. 400
Does treatment of vulvar lichen sclerosus influence its prognosis? 400
Topical testosterone versus clobetasol for vulvar lichen sclerosus. 400
Second-line therapies 400
Lichen sclerosus of the male genitalia and urethra: surgical options and results in a multi-centre international experience of 215 patients. 400
Perineoplasty for the treatment of introital stenosis related to vulvar lichen sclerosus. 400
Multicentre, phase II trial on the safety and efficacy of topical tacrolimus ointment for the treatment of lichen sclerosus. 400
A double-blind, randomized controlled trial of clobetasol versus pimecrolimus in patients with vulvar lichen sclerosus. 400
Third-line therapies 400
Acitretin for severe lichen sclerosus of male genitalia: a randomized, placebo controlled study. 400
Is carbon dioxide laser treatment of lichen sclerosus effective in the long run? 400
Genital lichen sclerosus treated by carbon dioxide laser. 401
Other therapies 401
Low-dose ultraviolet A1 phototherapy for extragenital lichen sclerosus: results of a preliminary study. 401
UVA1 phototherapy for genital lichen sclerosus. 401
Open-label trial of cyclosporine for vulvar lichen sclerosus. 401
Response of vulval lichen sclerosus and squamous hyperplasia to photodynamic treatment using sustained topical delivery of aminolevulinic acid from a novel bioadhesive patch system. 401
Treatment of lichen sclerosus with antibiotics. 401
131 Lichen simplex chronicus 402
Management strategy 402
Specific investigations 402
First-line therapies 402
A double-blind, multicenter trial of 0.05% halobetasol propionate ointment and 0.05% clobetasol 17-propionate ointment in the treatment of patients with chronic, localized atopic dermatitis or lichen simplex chronicus. 403
A review of two controlled multicenter trials comparing 0.05% halobetasol propionate ointment to its vehicle in the treatment of chronic eczematous dermatoses. 403
Flurandrenolone tape in the treatment of lichen simplex chronicus. 403
Update on intralesional steroid: focus on dermatoses. 403
Second-line therapies 403
The antipruritic effect of 5% doxepin cream in patients with eczematous dermatitis. 403
Pimecrolimus 1% cream for pruritus in postmenopausal diabetic women with vulvar lichen simplex chronicus: a prospective non-controlled case series. 403
Treatment of prurigo nodularis, chronic prurigo and neurodermatitis circumscripta with topical capsaicin. 403
Cryosurgical treatment of nodular neurodermatitis with Refrigerant 12. 403
Topical tacrolimus for the treatment of lichen simplex chronicus. 403
Third-line therapies 403
Transcutaneous electrical nerve stimulation for reduction of pruritus in macular amyloidosis and lichen simplex. 404
Effectiveness of ketotifen in the treatment of neurodermatitis in childhood. 404
Acupuncture treatment of 139 cases of neurodermatitis. 404
Botulinum toxin type A injection in the treatment of lichen simplex: an open pilot study. 404
The effect of topically applied aspirin on localized circumscribed neurodermatosis. 404
Therapeutic hotline: treatment of prurigo nodularis and lichen simplex chronicus with gabapentin. 404
The behavioral treatment of neurodermatitis through habit-reversal. 404
Brief hypnotherapy of neurodermatitis: a case with 4-year followup. 404
Improvement of chronic neurotic excoriations with oral doxepin therapy. 404
Nodular lichen simplex of the scrotum treated by surgical excision. 404
132 Linear IgA bullous dermatosis 405
Management strategy 405
Specific investigations 405
Linear IgA disease in adults. 405
A clinicopathological study of mucosal involvement in linear IgA disease. 405
Cicatrizing conjunctivitis as predominant manifestation of linear IgA bullous dermatosis. 406
Chronic bullous disease of childhood, childhood cicatricial pemphigoid, and linear IgA disease of adults. A comparative study demonstrating clinical and immunopathologic overlap. 406
Linear immunoglobulin A bullous dermatosis. 406
Vancomycin-induced linear IgA bullous dermatosis. 406
First-line therapies 406
Linear IgA dapsone responsive bullous dermatosis. 406
Second-line therapies 406
Colchicine as a novel therapeutic agent in chronic bullous dermatosis of childhood. 406
Treatment of pemphigus and linear IgA dermatosis with nicotinamide and tetracycline. 406
Sublamina densa-type linear IgA bullous dermatosis successfully treated with oral tetracycline and niacinamide. 406
Third-line therapies 406
Sulphamethoxypridazine for dermatitis herpetiformis, linear IgA disease, and cicatricial pemphigoid. 406
Treatment of chronic bullous dermatosis of childhood with oral dicloxacillin. 406
Chronic bullous disease of childhood: successful treatment with dicloxacillin. 406
Mixed immunobullous disease of childhood: a good response to antimicrobials. 406
Linear IgA bullous dermatosis responsive to trimethoprim-sulfamethoxazole. 406
Linear IgA disease: successful treatment with erythromycin. 406
Treatment of linear IgA bullous dermatosis of childhood with flucloxacillin. 406
Treatment of linear IgA bullous dermatosis of childhood with mycophenolate mofetil. 406
Successful treatment of oral linear IgA disease using mycophenolate. 406
Methotrexate and cyclosporine are of value in the treatment of adult linear IgA disease. 407
Linear IgA disease: successful treatment with cyclosporine. 407
Interferon alpha for linear IgA bullous dermatosis. 407
High-dose intravenous immune globulin is also effective in linear IgA disease. 407
Successful treatment of linear IgA disease with salazosulphapyridine and intravenous immunoglobulins. 407
Upper aerodigestive tract complications in a neonate with linear IgA bullous dermatosis. 407
High-dose intravenous immunoglobulins for the treatment of autoimmune mucocutaneous blistering diseases: evaluation of its use in 19 cases. 407
Linear IgA bullous dermatosis of childhood: response to thalidomide. 407
Linear IgA disease: successful application of immunoadsorption and review of the literature. 407
133 Lipodermatosclerosis 408
Management strategy 408
Specific investigations 408
The clinical spectrum of lipodermatosclerosis. 408
Lipodermatosclerosis: the histologic spectrum with clinical correlation to the acute and chronic forms. 408
Lipodermatosclerosis: a clinicopathological study of 25 cases. 408
Skin iron deposition characterises lipodermatosclerosis and leg ulcer. 408
Duplex venous imaging: role for a comprehensive lower extremity examination. 408
Results of duplex scanning of 205 lower extremities with varices: 106 not previously operated and 99 previously operated for varicose veins. 408
Quantifying fibrosis in venous disease: mechanical properties of lipodermatosclerosis and healthy tissue. 408
Excision of lipodermatosclerotic tissue: an effective treatment for non-healing venous ulcer. 409
Microangiopathy in chronic venous insufficiency: quantitative assessment by capillary microscopy. 409
Magnetic resonance imaging as a diagnostic tool for extensive lipodermatosclerosis. 409
First-line therapies 409
The clinical spectrum of lipodermatosclerosis. 409
Graduated compression stockings reduce lipodermatosclerosis and ulcer recurrence. 409
Removal of dermal edema with class I and II compression stockings in patients with lipodermatosclerosis. 409
Venous lipodermatosclerosis: treatment by fibrinolytic enhancement and elastic compression. 409
Acute lipodermatosclerosis: an open clinical trial of stanozolol in patients unable to sustain compression. 409
HR (Paroven, Venoruton; O-(beta-hydroxyethyl)- rutosides) in venous hypertensive microangiopathy. 409
Second-line therapies 409
Pentoxifylline for treating venous leg ulcer. 409
Comparison of surgery and compression with compression alone in chronic venous ulceration (ESCHAR study): randomized controlled trial. 409
Third-line therapies 409
Lipid lowering and enhancement of fibrinolysis with niacin. 409
Early benefit of subfascial endoscopic perforator surgery (SEPS) in healing venous ulcer. 409
The effect of ultrasound-guided sclerotherapy (UGS) of incompetent perforator veins on venous clinical severity and disability scores. 410
Hypodermatitis sclerodermiformis. 410
Ultrasound therapy for lipodermatosclerosis. 410
Excision of lipodermatosclerotic tissue: an effective treatment for non-healing venous ulcer. 410
Surgical removal of ulcer and dermatosclerosis followed by split-skin grafting yields long-term results in ‘non-healing’ venous leg ulcers. 410
Hypodermatitis sclerodermiformis and unusual acid-fast bacteria. 410
Severe chronic venous insufficiency treated by foamed sclerosant. 410
Intralesional triamcinolone in the management of lipodermatosclerosis. 410
Refractory lipodermatosclerosis treated with intralesional platelet-rich plasma. 410
Topical capsaicin for the treatment of acute lipodermatosclerosis and lobular panniculitis. 410
An acute case of lipodermatosclerosis successfully treated with danazol. 410
Lipodermatosclerosis: Successful treatment with danazol. 410
Treatment of lipodermatosclerosis with oxandrolone in a patient with stanozolol-induced hepatotoxicity. 410
134 Livedo reticularis 411
Management strategy 411
Specific investigations 411
Livedo reticularis and related disorders. 411
Livedo reticularis: an update. 411
The histopathological characteristics of livedo reticularis. 412
Diagnostic impact and sensitivity of skin biopsies in Sneddon’s syndrome. A report of 15 cases. 412
Livedo reticularis: an underutilized diagnostic clue in cholesterol embolization syndrome. 412
The spectrum of livedo reticularis and anticardiolipin antibodies. 412
First-line therapy 412
Sneddon’s syndrome: generalized livedo reticularis and cerebrovascular disease – importance of hemostatic screening. 412
Second-line therapies 412
Cholesterol emboli syndrome in type 2 diabetes: the disease history of a case evaluated with renal scintigraphy. 412
Livedo reticularis and livedoid vasculitis responding to PUVA therapy. 412
Widespread livedoid vasculopathy. 412
Third-line therapies 412
Livedo reticularis caused by cholesterol embolization may improve with simvastatin. 412
Minocycline induced arthritis associated with fever, livedo reticularis and pANCA. 412
Livedo reticularis associated with interferon α therapy in two melanoma patients. 413
135 Livedoid vasculopathy 414
Management strategy 414
Specific investigations 414
Association between peripheral vascular endothelial dysfunction and livedoid vasculopathy. 414
Livedoid vasculopathy: an intriguing cutaneous disease. 414
Livedoid vasculopathy: further evidence for procoagulant pathogenesis. 414
Livedoid vasculopathy: what is it and how the patient should be evaluated and treated. 414
Livedoid vasculopathy: the role of hyperhomocysteinemia and its simple therapeutic consequences. 415
Livedo (livedoid) vasculitis and the factor V Leiden mutation: additional evidence for abnormal coagulation. 415
Livedoid vasculopathy associated with heterozygous protein C deficiency. 415
Livedoid vasculitis: a manifestation of the antiphospholipid syndrome? 415
Atrophie blanche: a disorder associated with defective release of tissue plasminogen activator. 415
First-line therapies 415
Atrophie blanche: a clinicopathological study of 27 patients. 415
Livedoid vasculopathy associated with sickle cell trait: significant improvement on aspirin treatment. 415
Livedo vasculitis: therapy with pentoxifylline. 415
Second-line therapies 415
Frequency of thrombophilia determinant factors in patients with livedoid vasculopathy and treatment with anticoagulant drugs – a prospective study. 415
Livedoid vasculopathy in a pediatric patient with elevated lipoprotein(a) levels: prompt response to continuous low-molecular-weight heparin. 415
Treatment of livedoid vasculopathy with low-molecular-weight heparin: report of 2 cases. 415
Difficult management of livedoid vasculopathy. 415
Ulcerations caused by livedoid vasculopathy associated with a prothrombotic state: response to warfarin. 415
A case of livedoid vasculopathy associated with factor V Leiden mutation: successful treatment with oral warfarin. 415
Warfarin therapy for livedoid vasculopathy associated with cryofibrinogenemia and hyperhomocysteinemia. 416
Livedoid vasculopathy: long-term follow-up results following hyperbaric oxygen therapy. 416
Low-dose danazol in the treatment of livedoid vasculitis. 416
Livedoid vasculitis with anticardiolipin antibodies: improvement with danazol. 416
Third-line therapies 416
Livedoid vasculopathy associated with plasminogen activator inhibitor-1 promoter homozygosity (4G/4G) treated successfully with tissue plasminogen activator. 416
Tissue plasminogen activator for treatment of livedoid vasculitis. 416
Successful long-term use of intravenous immunoglobulin to treat livedoid vasculopathy associated with plasminogen activator inhibitor-1 promoter homozygosity. 416
Pulsed intravenous immunoglobulin therapy in livedoid vasculitis: an open trial evaluating 9 consecutive patients. 416
Livedoid vasculitis responding to PUVA therapy. 416
Clinical studies of livedoid vasculitis (segmental hyalinizing vasculitis). 416
Livedoid vasculopathy with combined thrombophilia: efficacy of iloprost (French). 416
136 Lyme borreliosis 417
Management strategy 417
Early localized Lyme disease 417
Early disseminated Lyme disease 417
Late Lyme disease 418
Post-treatment symptoms 418
Re-infection and vaccination 418
Lyme borelliosis. 418
Lyme disease: Part I. Advances and perspectives. 418
Lyme disease: Part II. Management and prevention. 418
Specific investigations 418
Testing 418
Prospective study of serologic tests for Lyme disease. 418
Prevention 418
Peridomestic Lyme disease prevention. Results of a population based case-control study. 418
Prophylaxis 418
Prophylaxis with single-dose doxycycline for the prevention of Lyme disease after an Ixodes scapularis tick bite. 418
Treatment 418
The clinical assessment, treatment, and prevention of Lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America. 418
First-line therapies 419
Second-line therapies 419
Amoxicillin plus probenecid versus doxycycline for treatment of erythema migrans borreliosis. 419
Comparison of cefuroxime axetil and doxycycline in the treatment of early Lyme disease. 419
Two controlled trials of antibiotic treatment in patients with persistent symptoms and a history of Lyme disease. 419
Azithromycin compared with amoxicillin in the treatment of erythema migrans. A double-blind, randomized, controlled trial. 419
Duration of antibiotic therapy for early Lyme disease. 419
Antibiotic treatment duration and long-term outcomes of patients with early Lyme disease from a Lyme disease hyperendemic area. 419
137 Lymphangioma circumscriptum 420
Management strategies 420
Specific investigations 420
First-line therapies 420
OK-432 therapy in 64 patients with lymphangioma. 421
A case of unresectable lymphangioma circumscriptum of the vulva successfully treated with OK-432 in childhood. 421
138 Lymphedema 423
Management strategies 423
Specific investigations 423
Advances in imaging of lymph flow disorders. 423
Indocyanine green (ICG) lymphography is superior to lymphoscintigraphy for diagnostic imaging of early lymphedema of the upper limbs. 423
First-line therapies 423
Prospective trial of intensive decongestive physiotherapy for upper extremity lymphedema. 423
Synergic effect of compression therapy and controlled active exercises using a facilitating device in the treatment of arm lymphedema. 424
Primary lymphedema: clinical features and management in 138 pediatric patients. 424
Can manual treatment of lymphedema promote metastasis? 424
Second-line therapies 424
Direct evidence of lymphatic function improvement after advanced pneumatic compression device treatment of lymphedema. 424
Third-line therapies 424
Microsurgery for lymphedema: clinical research and long-term results. 424
Overview of surgical treatments for breast cancer-related lymphedema. 424
Pediatric lymphedema and correlated syndromes: role of microsurgery. 424
Treatment of post-mastectomy lymphedema with laser therapy: double blind placebo control randomized study. 424
139 Lymphocytoma cutis 425
Management strategy 425
Specific investigations 425
The spirochetal etiology of lymphadenosis benigna cutis solitaria. 425
Lymphadenosis benigna cutis resulting from Borrelia infection (Borrelia lymphocytoma). 425
Cutaneous lymphoid hyperplasia and cutaneous marginal zone lymphoma: comparison of morphologic and immunophenotypic features. 425
Differential diagnosis of cutaneous infiltrates of B lymphocytes with follicular growth pattern. 426
Borrelia burgdorfori-associated lymphocytoma cutis: clinicopathologic, immunophenotypic, and molecular study of 106 cases. 426
Clonal rearrangements of immunoglobulin genes and progression to B cell lymphoma in cutaneous lymphoid hyperplasia. 426
Immunophenotypic and genotypic analysis in cutaneous lymphoid hyperplasias. 426
Polymerase chain reaction analysis of immunoglobulin gene rearrangement analysis in cutaneous lymphoid hyperplasias. 426
A review of 55 cases of cutaneous lymphoid hyperplasia: reassessment of the histopathologic findings leading to reclassification of 4 lesions as cutaneous marginal zone lymphoma and 19 as pseudolymphomatous folliculitis. 426
Lymphomatoid contact reaction to gold earrings. 426
First-line therapies 426
Treatment of cutaneous pseudolymphoma with hydroxychloroquine. 426
A study of the photosensitivity factor in cutaneous lymphocytoma. 426
Cutaneous lymphoid hyperplasia (pseudolymphoma) in tattoos: a case series of 7 patients. 426
Second-line therapies 426
Cutaneous lymphoid hyperplasia: results of radiation therapy. 427
Local orthovolt radiotherapy in primary cutaneous B-cell lymphoma. 427
Role of the argon laser in treatment of lymphocytoma cutis. 427
Lymphocytoma cutis: a series of five patients successfully treated with cryosurgery. 427
Spiegler–Fendt type lymphocytoma cutis: a case report of two patients successfully treated with interferon alpha-2b. 427
Treatment of cutaneous lymphoid hyperplasia with thalidomide: report of two cases. 427
Lymphocytoma cutis treated with topical tacrolimus. 427
Treatment of cutaneous lymphoid hyperplasia with the monoclonal anti-CD20 antibody rituximab. 427
Successful treatment of lymphadenosis benigna cutis with topical photodynamic therapy with delta-aminolevulinic acid. 427
Topical 5-aminolevulinic acid-based photodynamic therapy for the treatment of a patient with cutaneous pseudolymphoma. 427
140 Lymphogranuloma venereum 428
Management strategy 428
Specific investigations 428
Update on lymphogranuloma venereum in the United Kingdom. 428
Diagnostic and clinical implications of anorectal lymphogranuloma venereum in men who have sex with men: a retrospective case-control study. 428
Lymphogranuloma venereum presenting as perianal ulceration: an emerging clinical presentation? 428
Lymphogranuloma venereum. 428
The association between lymphogranuloma venereum and HIV among men who have sex with men: systematic review and meta-analysis. 429
Reactive arthritis associated with proctitis due to Chalmydia trachomatis serovar L2b. 429
Persistent high-risk sexual behavior in men who have sex with men after symptomatic lymphogranuloma venereum proctitis. 429
Lymphogranuloma venereum proctitis masquerading as inflammatory bowel disease in 12 homosexual men. 429
First-line therapies 429
Sexually transmitted diseases treatment guidelines 2006. 429
Second-line therapies 429
Treatment of lymphogranuloma venereum. 429
Doxycycline failure in lymphogranuloma venereum. 429
An audit on the management of lymphogranuloma venereum in a sexual health clinic in London, UK. 429
Lymphogranuloma venereum. 429
Third-line therapies 429
141 Lymphomatoid papulosis 430
Management strategy 430
Specific investigations 430
Spectrum of primary cutaneous CD30 (Ki-1)-positive lymphoproliferative disorders. A proposal for classification and guidelines for management and treatment. 430
Lymphomatoid papulosis. Reappraisal of clinicopathologic presentation and classification into subtypes A, B, and C. 430
A variant of lymphomatoid papulosis simulating primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma. Description of 9 cases. 431
WHO-EORTC classification for cutaneous lymphomas. 431
Clinicopathologic challenge: acral lymphomatoid papulosis. 431
Primary and secondary cutaneous CD30+ lymphoproliferative disorders: a report from the Dutch Cutaneous Lymphoma Group on the long-term follow-up data of 219 patients and guidelines for diagnosis and treatment. 431
Lymphomatoid papulosis and associated lymphomas: a retrospective case series of 84 patients. 431
CD30+ cutaneous lymphoproliferative disorders: the Stanford experience in lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma. 431
Increased risk of lymphoid and nonlymphoid malignancies in patients with lymphomatoid papulosis. 431
Cutaneous hematologic disorders in children. 431
Lymphomatoid papulosis in children: a retrospective cohort study of 35 cases. 431
Single cell analysis of CD30+ cells in lymphomatoid papulosis demonstrates a common clonal T-cell origin. 432
Lymphomatoid papulosis associated with mycosis fungoides: a study of 21 patients including analyses for clonality. 432
CD30-positive T-cell lymphoproliferative disorder of the oral mucosa – an indolent lesion: Report of 4 cases. 432
Lymphomatoid papulosis in a patient with Crohn’s disease treated with infliximab. 432
Large cell transformation mimicking regional lymphomatoid papulosis in a patient with mycosis fungoides. 432
In search of prognostic indicators for lymphomatoid papulosis: a retrospective study of 123 patients. 432
First-line therapies 432
EORTC, ISCL, and USCLC consensus recommendations for the treatment of primary cutaneous CD30-positive lymphoproliferative disorders: lymphomatoid papulosis and primary cutaneous anaplastic large-cell lymphoma. 432
PUVA-treatment in lymphomatoid papulosis. 432
Medium-dose UVA1 therapy of lymphomatoid papulosis. 432
Methotrexate is effective therapy for lymphomatoid papulosis and other primary cutaneous CD30+ lymphoproliferative disorders. 432
Lymphomatoid papulosis: successful weekly pulse superpotent topical corticosteroid therapy in three pediatric patients. 433
Second-line therapies 433
Long-term efficacy, curative potential, and carcinogenicity of topical mechlorethamine chemotherapy in cutaneous T cell lymphoma. 433
Topical carmustine therapy for lymphomatoid papulosis. 433
Third-line therapies 433
Bexarotene is a new treatment option for lymphomatoid papulosis. 433
Therapeutic use of interferon-alpha for lymphomatoid papulosis. 433
308-nm excimer laser for the treatment of lymphomatoid papulosis and stage IA mycosis fungoides. 433
Persistent agmination of lymphomatoid papulosis: an equivalent of limited plaque mycosis fungoides type of cutaneous T-cell lymphoma. 433
Treatment of lymphomatoid papulosis with imiquimod 5% cream. 433
A phase 2 study of SGN-30 in cutaneous anaplastic large cell lymphoma and related lymphoproliferative disorders. 434
Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas. 434
Results of a pivotal phase II study of brentuximab vedotin for patients with relapsed or refractory Hodgkins lymphoma. 434
142 Malignant atrophic papulosis 435
Specific investigations 435
First-line therapies 436
Degos disease: a C5b-9/interferon-α-mediated endotheliopathy syndrome. 436
Commentary on Degos disease: a C5b-9/interferon-α-mediated endotheliopathy syndrome by Magro et al: a reconsideration of Degos disease as hematologic or endothelial genetic disease. 436
Second-line therapies 436
Malignant atrophic papulosis. 436
Malignant atrophic papulosis: treatment with aspirin and dipyridamole. 436
Malignant atrophic papulosis in an infant. 436
Effect of fibrinolytic treatment in malignant atrophic papulosis. 436
Penile ulceration in fatal malignant atrophic papulosis (Degos’ disease). 436
A case of malignant atrophic papulosis successfully treated with nicotine patches. 436
Third-line therapies 436
Inefficacy of intravenous immunoglobulins and infliximab in Degos’ disease. 436
The use of intravenous immunoglobulin in cutaneous and recurrent perforating intestinal Degos disease (malignant atrophic papulosis). 436
A fatal case of malignant atrophic papulosis (Degos’ disease) in a man with factor V Leiden mutation and lupus anticoagulant. 436
A case of systemic malignant atrophic papulosis (Köhlmeier-Degos’ disease). 436
Malignant atrophic papulosis of Degos. Report of a patient who failed to respond to fibrinolytic therapy. 437
Benign familial Degos disease worsening during immunosuppression. 437
[An autopsy case of Degos’ disease with ascending thoracic myelopathy]. 437
143 Malignant melanoma 438
Management strategy 438
Specific investigations 439
Final version of 2009 American Joint Committee on Cancer (AJCC) melanoma staging and classification. 439
National Comprehensive Cancer Network. Clinical practice guidelines in oncology. V 1.2013. 439
Incisional biopsy and melanoma prognosis. 439
Technical details of intraoperative lymphatic mapping. 439
The role of sentinel lymph node biopsy for melanoma: evidence assessment. 439
Atlas of Dermoscopy. 440
The performance of MelaFind: a prospective multicenter study. 440
First-line therapies 440
Surgical margins for melanoma in situ. 440
Long-term results of a prospective surgical trial comparing 2 cm vs. 4 cm excision margins for 740 patients with 1–4 mm melanomas. 440
Excision margins in high-risk malignant melanoma. 440
Overview and update of the phase III Multicenter Selective Lymphadenectomy Trials (MSLT-I and MSLT-II) in melanoma. 440
Elective lymph node dissection in patients with melanoma: systematic review and meta-analysis of randomized controlled trials. 440
Second-line therapies 440
Adjuvant therapy with pegylated interferon alfa-2b versus observation alone in resected stage III melanoma: final results of EORTC 18991, a randomised phase III trial. 440
Combination of paclitaxel and carboplatin as second-line therapy for patients with metastatic melanoma. 441
Locoregional cutaneous metastases of malignant melanoma and their management. 441
High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993. 441
Durable complete responses with high-dose bolus interleukin-2 in patients with metastatic melanoma who have experienced progression after biochemotherapy. 441
Management of in-transit melanoma of the extremity with isolated limb perfusion. 441
Bcl-2 antisense (oblimersen sodium) plus dacarbazine in patients with advanced melanoma: The Oblimersen Melanoma Study Group. 441
Improved survival with ipilimumab in patients with metastatic melanoma. 441
Ipilimumab plus dacarbazine for previously untreated metastatic melanoma. 441
Inhibition of mutated, activated BRAF in metastatic melanoma. 441
Improved survival with vemurafenib in melanoma with BRAF V600E mutation. 441
Improved survival with MEK inhibition in BRAF-mutated melanoma. 442
KIT as a therapeutic target in metastatic melanoma. 442
Third-line therapies 442
The benefits of adjuvant radiation therapy after therapeutic lymphadenectomy for clinically advanced, high-risk, lymph node-metastatic melanoma. 442
Mohs micrographic surgery for the treatment of melanoma. 442
144 Mastocytoses 443
Management strategy 443
Specific investigations 443
Diagnostic value of tryptase in anaphylaxis and mastocytosis. 443
IL-6 levels predict disease variant and extent of organ involvement in patients with mastocytosis. 443
Surrogate markers of disease in mastocytosis. 444
Histologische Charakteristika und Häufigkeit der sekundaren Osteoporose bei systemischer Mastozytose: Eine retrospektive Analyse an 158 Fällen. 444
First-line therapies 444
Comparison of azelastine and chlorpheniramine in the treatment of mastocytosis. 444
Comparison of the therapeutic efficacy of cromolyn sodium with that of combined chlorpheniramine and cimetidine in systemic mastocytosis: results of a double-blind clinical trial. 444
Systemic mastocytosis treated with histamine H1 and H2 receptor antagonists. 444
Cimetidine in systemic mastocytosis. 444
Oral disodium cromoglycate in the treatment of systemic mastocytosis. 444
Urticaria pigmentosa treated with oral disodium cromoglycate. 444
Second-line therapies 444
Treatment of urticaria pigmentosa with corticosteroids. 444
Urticaria pigmentosa: systemic evaluation and successful treatment with topical steroids. 444
Bullous mastocytosis treated with oral betamethasone therapy. 445
Mastocytoma: topical corticosteroid treatment. 445
Solitary mastocytoma improved by intralesional injections of steroid. 445
Indolent systemic mastocytosis treated with narrow-band UVB phototherapy: study of five cases. 445
Photochemotherapy (PUVA) in the treatment of urticaria pigmentosa. 445
Short- and long-term effectiveness of oral and bath PUVA therapy in urticaria pigmentosa and systemic mastocytosis. 445
Photochemotherapy of dominant, diffuse, cutaneous mastocytosis. 445
Telangiectasia macularis eruptive perstans successfully treated with PUVA therapy. 445
Medium- versus high-dose ultraviolet A1 therapy for urticaria pigmentosa: a pilot study. 445
Third-line therapies 445
Treatment of urticaria pigmentosa using interferon alpha. 445
Cutaneous mastocytosis: two pediatric patients treated with topical pimecrolimus. 445
Leukotriene-receptor inhibition for the treatment of systemic mastocytosis. 445
Response to cyclosporine and low-dose methylprednisolone in aggressive systemic mastocytosis. 446
Urticaria pigmentosa responsive to nifedipine. 446
Thalidomide in advanced mastocytosis. 446
Solitary mastocytoma in an adult: treatment by excision. 446
Treatment of an unusual solitary mast cell lesion with the pulsed dye laser resulting in cosmetic improvement and reduction in the degree of urticarial reaction. 446
The treatment of urticaria pigmentosa with the frequency-doubled Q-switch ND-YAG laser. 446
The cosmetic treatment of uticaria pigmentosa with Nd-YAG laser at 532 nanometers. 446
Treatment of telangiectasia macularis eruptiva perstans with total electron beam radiation. 446
Complete response after imatinib mesylate therapy in a patient with well-differentiated systemic mastocytosis. 446
Cladribine therapy for systemic mastocytosis. 446
Successful treatment of cutaneous mastocytosis and Ménière disease with anti-IgE therapy. 446
145 Melasma 447
Management strategy 447
Specific investigations 447
Association of melasma with thyroid autoimmunity and other thyroidal abnormalities and their relationship to the origin of the melasma. 447
First-line therapies 447
Melasma: a comprehensive update: part II. 447
Interventions for melasma. 447
Efficacy and safety of a new triple-combination agent for the treatment of facial melasma. 447
A randomized controlled trial of the efficacy and safety of a triple fixed combination (fluocinolone acetonide 0.01%, hydroquinone 4%, tretinoin 0.05%) compared with hydroquinone 4% cream in Asian patients with moderate to severe melasma. 447
A histological examination for skin atrophy after 6 months of treatment with fluocinolone acetonide 0.01%, hydroquinone 4%, and tretinoin 0.05% cream. 448
Topical tretinoin (retinoic acid) improves melasma. A vehicle-controlled, clinical trial. 448
Adapalene in the treatment of melasma: a preliminary report. 448
The efficacy of a broad-spectrum sunscreen in the treatment of melasma. 448
Second-line therapies 448
The treatment of melasma: 20% azelaic acid versus 4% hydroquinone cream. 448
Combined use of 20% azelaic acid cream and 0.05% tretinoin cream in the topical treatment of melasma. 448
Efficacy and safety of serial glycolic acid peels and a topical regimen in the treatment of recalcitrant melasma. 448
Third-line therapies 448
Evaluation of efficacy and safety of rucinol serum in patients with melasma: a randomized controlled trial. 448
Efficacy and safety of liposome-encapsulated 4-n-butyl resorcinol 0.1% cream for the treatment of melasma: a randomized controlled split-face trial. 448
Comparison of 30% salicylic acid with Jessner’s solution for superficial chemical peeling in epidermal melasma. 448
A double-blind, randomized clinical trial of niacinamide 4% versus hydroquinone 4% in the treatment of melasma. 449
Treatment of melasma using kojic acid in a gel containing hydroquinone and glycolic acid. 449
Topical liquiritin improves melasma. 449
Nonablative 1550-nm fractional laser therapy versus triple topical therapy for the treatment of melasma: a randomized controlled pilot study. 449
Low-fluence Q-switched neodymium-doped yttrium aluminum garnet (1064 nm) laser for the treatment of facial melasma in Asians. 449
Sequential treatment with triple combination cream and intense pulsed light is more efficacious than sequential treatment with an inactive (control) cream and intense pulsed light in patients with moderate to severe melasma. 449
Treatment of melasma with oral administration of tranexamic acid. 449
146 Merkel cell carcinoma 450
Management strategy 450
Specific investigations 450
Interest of (18)F-FDG PET-CT scanning for staging and management of Merkel cell carcinoma: a retrospective study of 15 patients. 450
Recurrence and survival in patients undergoing sentinel lymph node biopsy for Merkel cell carcinoma: analysis of 153 patients from a single institution. 450
Sentinel lymph node biopsy for evaluation and treatment of patients with Merkel cell carcinoma: the Dana-Farber experience and meta-analysis of the literature. 450
First-line therapies 451
Merkel cell carcinoma. Comparison of Mohs micrographic surgery and wide excision in eighty-six patients. 451
Five hundred patients with Merkel cell carcinoma evaluated at a single institution. 451
Second-line therapies 451
Merkel cell carcinoma: an Australian perspective and the importance of addressing the regional lymph nodes in clinically node-negative patients. 451
Adjuvant radiation therapy is associated with improved survival in Merkel cell carcinoma of the skin. 451
Multimodality treatment of Merkel cell carcinoma: case series and literature review of 1024 cases. 451
Treatment of recurrent Merkel cell carcinoma: an analysis of 46 cases. 451
In-transit Merkel cell carcinoma treated with isolated limb perfusion or isolated limb infusion: a case series of 12 patients. 451
147 Methicillin-resistant Staphylococcus aureus (MRSA) 452
Management strategy 452
Specific investigations 452
The prevalence, genotype and antimicrobial susceptibility of high- and low-level mupirocin resistant methicillin- resistant Staphylococcus aureus. 452
Mupirocin resistance in Staphylococcus aureus causing recurrent skin and soft tissue infections in children. 452
Clinical importance of purulence in methicillin-resistant Staphylococcus aureus skin and soft tissue infections. 452
Susceptibility testing and resistance phenotype detection in Staphylococcus aureus strains isolated from patients with atopic dermatitis, with apparent and recurrent skin colonization. 452
Cost-analysis of PCR-guided pre-emptive antibiotic treatment of Staphylococcus aureus infections: an analytic decision model. 453
High vancomycin minimum inhibitory concentration is a predictor of mortality in methicillin-resistant Staphylococcus aureus bacteremia. 453
Is methicillin-resistant Staphylococcus aureus involved in community acquired skin and soft tissue infections? Experience from a tertiary care centre in Mumbai. 453
First-line therapy 453
Randomized controlled trial of cephalexin versus clindamycin for uncomplicated pediatric skin infections. 453
Dose of trimethoprim–sulfamethoxazole to treat skin and skin structure infections caused by methicillin-resistant Staphylococcus aureus. 453
Comparative effectiveness of antibiotic treatment strategies for pediatric skin and soft-tissue infections. 453
An alternative to open incision and drainage for community-acquired soft tissue abscesses in children. 453
Children with atopic dermatitis appear less likely to be infected with community acquired methicillin-resistant Staphylococcus aureus: the San Diego experience. 454
Antimicrobial susceptibility of Staphylococcus aureus in children with atopic dermatitis. 454
Trimethoprim–sulfamethoxazole or clindamycin for community-associated MRSA (CA-MRSA) skin infections. 454
Characterization of Staphylococcus aureus cutaneous infections in a pediatric dermatology tertiary health care outpatient facility. 454
Randomized, controlled trial of antibiotics in the management of community-acquired skin abscesses in the pediatric patient. 454
Trimethoprim–sulfamethoxazole or clindamycin for treatment of community-acquired methicillin-resistant Staphylococcus aureus skin and soft tissue infections. 454
Prospective investigation of nasal mupirocin, hexachlorophene body wash, and systemic antibiotics for prevention of recurrent community-associated methicillin-resistant Staphylococcus aureus infections. 454
Targeted intranasal mupirocin to prevent colonization and infection by community-associated methicillin-resistant Staphylococcus aureus strains in soldiers: a cluster randomized controlled trial. 454
Second-line therapy 454
Linezolid and vancomycin in treatment of lower-extremity complicated skin and skin structure infections caused by methicillin-resistant Staphylococcus aureus in patients with and without vascular disease. 455
Antimicrobial susceptibility and molecular characteristics of 857 methicillin-resistant Staphylococcus aureus isolates from 16 medical centers in Japan (2008–2009): nationwide survey of community-acquired and nosocomial MRSA. 455
Nasal carriage of methicillin resistant Staphylococcus aureus and their antibiotic susceptibility patterns in children attending day-care centers. 455
Cost-effectiveness analysis of linezolid, daptomycin, and vancomycin in methicillin-resistant Staphylococcus aureus: complicated skin and skin structure infection using Bayesian methods for evidence synthesis. 455
Retrospective cohort study of hospitalized adults treated with vancomycin or clindamycin for methicillin-resistant Staphylococcus aureus skin infections. 455
Zyvox Annual Appraisal of Potency and Spectrum program: linezolid surveillance program results for 2008. 455
A comparison of costs and hospital length of stay associated with intravenous/oral linezolid or intravenous vancomycin treatment of complicated skin and soft-tissue infections caused by suspected or confirmed methicillin-resistant Staphylococcus aureus in elderly US patients. 455
In vitro pharmacokinetic/pharmacodynamic activity of NXL103 versus clindamycin and linezolid against clinical Staphylococcus aureus and Streptococcus pyogenes isolates. 455
Multicenter evaluation of the in vitro activity of dalbavancin tested against staphylococci and streptococci in 5 European countries: results from the DECIDE Surveillance Program (2007). 455
Clinical experience with daptomycin in Italy: results from a registry study of the treatment of Gram-positive infections between 2006 and 2009. 456
Daptomycin experience in critical care patients: results from a registry. 456
Third-line therapies 456
Sustained antimicrobial activity of tigecycline against methicillin-resistant Staphylococcus aureus (MRSA) from United States Medical Centers from 2004 through 2008. 456
Activity of oritavancin and comparators in vitro against standard and high inocula of Staphylococcus aureus. 456
Antibacterial effects of plant-derived extracts on methicillin-resistant Staphylococcus aureus. 456
Rates of killing of methicillin-resistant Staphylococcus aureus by ceftaroline, daptomycin, and telavancin compared to that of vancomycin. 456
Results of a double-blind, randomized trial of ceftobiprole treatment of complicated skin and skin structure infections caused by Gram-positive bacteria. 456
Effect of medical honey on wounds colonised or infected with MRSA. 456
148 Miliaria 457
Management strategy 457
Specific investigations 457
Nonneoplastic disorders of the eccrine glands. 457
Duct disruption, a new explanation of miliaria. 457
The role of extracellular polysaccharide substance produced by Staphylococcus epidermidis in miliaria. 458
A novel finding in atopic dermatitis: film-producing Staphylococcus epidermidis as an etiology. 458
The pathogenesis of miliaria rubra: role of the resident microflora. 458
Miliaria crystallina in an intensive care setting. 458
Pruritus, papules and perspiration. 458
Miliaria-rash after neutropenic fever and induction chemotherapy for acute myelogenous leukemia. 458
Newborn with pseudohypoaldosteronism and miliaria rubra. 458
First-line therapies 458
Miliaria rubra of the lower limbs in underground miners. 458
Diseases of the eccrine and apocrine sweat glands. 458
Goosefleshlike lesions and hypohidrosis. 458
Congenital miliaria crystalline in a term neonate born to a mother with chorioamnionitis. 458
Second-line therapies 458
Miliaria rubra. 458
Heat illness: prickly heat. 458
Third-line therapies 459
Miliaria profunda. 459
The effects of administration of ascorbic acid in experimentally induced miliaria and hypohidrosis in volunteers. 459
Patients presenting with miliaria while wearing flame resistant clothing in high ambient temperatures: a case series. 459
149 Molluscum contagiosum 460
Management strategy 460
Specific investigations 460
First-line therapies 460
The natural history of molluscum contagiosum in Fijian children. 460
Scarring in molluscum contagiosum: comparison of physical expression and phenol ablation. 460
Second-line therapies 460
Molluscum contagiosum effectively treated with a topical acidified nitrite, nitric oxide liberating cream. 460
Topical therapy with salicylic gel as a treatment for molluscum contagiosum in children. 461
Molluscum contagiosum treated with iodine solution and salicylic acid plaster. 461
Treatment of molluscum contagiosum with silver nitrate paste. 461
Podophyllotoxin in the treatment of molluscum contagiosum. 461
Molluscum contagiosum in children: evidence-based treatment. 461
Third-line therapies 461
Treatment of molluscum contagiosum using a lidocaine/prilocaine cream (EMLA) for analgesia. 461
Curettage of molluscum contagiosum in children: analgesia by topical application of a lidocaine/prilocaine cream (EMLA). 461
Treatment of molluscum contagiosum with the pulsed dye laser over a 28-month period. 461
Treatment of molluscum contagiosum with a pulsed dye laser: pilot study with 19 children. 461
Photodynamic therapy for molluscum contagiosum infection in HIV-coinfected patients: review of 6 cases. 461
The successful use of ALA-PDT in the treatment of recalcitrant molluscum contagiosum. 461
Use of duct tape occlusion in the treatment of recurrent molluscum contagiosum. 461
Treatment of molluscum contagiosum with potassium hydroxide: a clinical approach in 35 children. 461
Double randomized, placebo-controlled study of the use of topical 10% potassium hydroxide solution in the treatment of molluscum contagiosum. 461
Comparative study of 5% potasssium hydroxide solution versus 0.05% tretinoin cream for molluscum contagiosum in children. 462
Treatment of molluscum contagiosum in males with an analogue of imiquimod 1% cream: a placebo controlled, double-blind study. 462
Treatment of molluscum contagiosum with imiquimod 5% cream. 462
Effectiveness of imiquimod cream 5% for treating childhood molluscum contagiosum in a double blind randomised pilot trial. 462
Topical treatment of molluscum contagiosum with imiquimod 5% in Turkish children. 462
Experience in treating molluscum contagiosum in children with imiquimod 5% cream. 462
Combination topical treatment of molluscum contagiosum with cantharidin and imiquimod 5% in children: a case series of 16 patients. 462
Pharmokinetics and safety of imiquimod 5% cream in the treatment of molluscum contagiosum. 462
Childhood molluscum contagiosum: experience with cantharidin therapy in 300 patients. 462
Treatment of molluscum contagiosum with topical diphencyprone therapy. 462
Essential oil of Australian lemon myrtle (Backhousia citriodora) in the treatment of molluscum contagiosum. 462
Topical cidofovir. A novel treatment for recalcitrant molluscum contagiosum in children infected with human immunodeficiency virus 1. 462
Cidofovir diphosphate inhibits molluscum contagiosum virus DNA polymerase activity. 462
Venereal herpes-like molluscum contagiosum: treatment with tretinoin. 462
Treatment of molluscum contagiosum: a brief review and discussion of a case successfully treated with adapalene. 462
Combination of essential oil of Melaleuca alternifolia and iodine in the treatment of molluscum contagiosum in children. 462
One-year experience with Candida antigen immunotherapy for warts and molluscum. 462
Treatment of molluscum contagiosum with oral cimetidine: clinical experience in 13 patients. 462
Interferon alpha treatment of molluscum contagiosum in immunodeficiency. 463
Interferon-alpha treatment of molluscum contagiosum in a patient with hyperimmunoglobulin E syndrome. 463
Resolution of disseminated molluscum contagiosum with highly active anti-retroviral therapy (HAART) in patients with AIDS. 463
Resolution of severe molluscum contagiosum on effective anti-retroviral therapy. 463
A prospective randomized trial comparing the efficacy and adverse effects of four recognized treatments of molluscum contagiosum in children. 463
150 Morphea 464
Management strategy 464
Initial evaluation 464
Treatment strategy 464
Treatments not supported by current evidence 464
Specific investigations 464
Development of consensus treatment plans for juvenile localized scleroderma. 464
Development and initial validation of the localized scleroderma skin damage index and physician global assessment of disease damage: a proof-of-concept study. 465
The use of Doppler ultrasound to evaluate lesions of localized scleroderma. 465
First-line therapies 465
A systematic review of morphea treatments and therapeutic algorithm. 465
Update on morphea part II. Outcome measures and treatment. 465
A randomized controlled study of low-dose UVA1, medium-dose UVA1, and narrowband UVB phototherapy in the treatment of localized scleroderma. 465
Medium-dose is more effective than low-dose ultraviolet A1 phototherapy for localized scleroderma as shown by 20-MHz ultrasound assessment. 465
Different low doses of broad-band UVA in treatment of morphea and systemic sclerosis. 465
Methotrexate treatment in juvenile localized scleroderma: a randomized, double-blinded, placebo-controlled trial. 465
Pulsed high-dose corticosteroids combined with low-dose methotrexate in severe localized scleroderma. 465
Localized scleroderma: response to occlusive treatment with tacrolimus ointment. 465
Efficacy of topical tacrolimus 0.1% in active plaque morphea: randomized, double-blind, emollient-controlled pilot study. 465
Second-line therapies 465
First case series on the use of calcipotriol-betamethasone dipropionate for morphoea. 466
Topical calcipotriene for morphea/linear scleroderma. 466
Successful treatment of severe or methotrexate-resistant juvenile localized scleroderma with mycophenolate mofetil. 466
UVA/UVA1 phototherapy and PUVA photochemotherapy in connective tissue diseases and related disorders: a research based review. 466
First case series on the use of imiquimod for morphoea. 466
Third-line therapies 466
Combining PUVA therapy with systemic immunosuppression to treat progressive diffuse morphoea. 466
Good response to linear scleroderma in a child to cyclosporine. 466
Adjunctive treatments/referrals 466
151 Mucoceles 467
Specific investigations 467
First-line therapies 467
A simple cryosurgical method for treatment of oral mucous cysts. 467
Histopathology of mucoceles infiltrated with steroids. 467
A review of common pediatric lip lesions: herpes simplex/recurrent herpes labialis, impetigo, mucoceles, and hemangiomas. 467
Clinical characteristics, treatment, and evolution of 89 mucoceles in children. 467
Second-line therapies 467
Two simple treatments for lower lip mucocoeles. 467
Third-line therapies 468
Treatment of mucocele of the lower lip with carbon dioxide laser. 468
Clinicostatistical study of lower lip mucoceles. 468
Conventional surgical treatment of oral mucocele: a series of 23 cases. 468
Clinical and histopathologic study of salivary mucoceles. 468
Treatment of mucus retention phenomena in children by the micro-marsupialization technique: case reports. 468
152 Mucous membrane pemphigoid 469
Management strategy 469
Interventions for mucous membrane pemphigoid and epidermolysis bullosa aquisitia. 469
The first international consensus on mucous membrane pemphigoid: definition, diagnostic criteria, pathogenic factors, medical treatment and prognostic indicators. 469
Specific investigations 469
First-line therapies 469
Mild disease 469
153 Mycetoma: 473
Management strategy 473
Specific investigations 473
Mycetoma: a thorn in the flesh. 474
Mycetoma caused by Madurella mycetomatis: a neglected infectious burden. 474
Mycetoma. 474
Emerging therapeutic regimes for the management of mycetomas. 474
First-line therapies 474
Actinomycetomas in Senegal. Study of 90 cases. 474
Mycetoma in children: experience with 15 cases. 474
A modified two-step treatment for actinomycetoma. 474
Clinical and mycologic findings and therapeutic outcome of 27 mycetoma patients from São Paulo, Brazil. 474
Improvement of eumycetoma with itraconazole. 474
Mycetoma in children. 474
The safety and efficacy of itraconazole for the treatment of patients with eumycetoma due to Madurella mycetomatis. 474
Second-line therapies 475
Treatment of actinomycetoma due to Nocardia spp. with amoxicillin–clavulanate. 475
Clinical efficacy and safety of oral terbinafine in fungal mycetoma. 475
Ketoconazole in the treatment of eumycetoma due to Madurella mycetomii. 475
Posaconazole treatment of refractory eumycetoma and chromoblastomycosis. 475
Efficacy of imipenem therapy for Nocardia actinomycetomas refractory to sulphonamides. 475
Madurella mycetomatis mycetoma treated successfully with oral voriconazole. 475
Scedosporium apiospermum mycetoma with bone involvement successfully treated with voriconazole. 475
Clinical experience with linezolid for the treatment of Nocardia infection. 475
Third-line therapies 475
Modified Welsh regimen: a promising therapy for actinomycetoma. 476
Scedosporium infection in immunocompromised patients: successful use of liposomal amphotericin B and itraconazole. 476
154 Mycobacterial (atypical) skin infections 477
Fish tank (swimming pool) granuloma 477
Management strategy 477
Specific investigations 477
First-line therapies 477
Epidemiological, clinical, and therapeutic pattern of Mycobacterium marinum infection: a retrospective series of 35 cases from southern France. 477
Sixty-three cases of Mycobacterium marinum infection. Clinical features, treatment and antibiotic susceptibility of causative isolates. 477
Soft tissue infections caused by marine bacterial pathogens: epidemiology, diagnosis, and management. 478
Nontuberculous mycobacterial infections of the skin: a retrospective study of 25 cases. 478
Atypical mycobacterial cutaneous infections in Hong Kong: 10 year retrospective study. 478
Cutaneous non-tuberculous mycobacterial infections: a clinical and histopathological study of 17 cases from Lebanon. 478
Second-line therapies 478
Third-line therapies 478
Treatment of Mycobacterium marinum cutaneous infections. 478
Efficacy of oral minocycline and hyperthermic treatment in a case of atypical mycobacterial skin infection by Mycobacterium marinum. 478
Possible role of anti-TNF monoclonal antibodies in the treatment of Mycobacterium marinum infection. 478
Mycobacterium marinum infection of the hand and wrist. 478
Mycobacterium ulcerans 478
Management strategy 479
Specific investigations 479
First-line therapies 479
Antimicrobial treatment for early, limited Mycobacterium ulcerans infection: a randomised controlled trial. 479
Clinical efficacy of combination of rifampin and streptomycin for treatment of Mycobacterium ulcerans disease. 479
Successful outcomes with oral fluoroquinolones combined with rifampicin in the treatment of Mycobacterium ulcerans: an observational cohort study. 479
Effect of a control project on clinical profiles and outcomes in Buruli ulcer: a before/after study in Bas-Congo, Democratic Republic of Congo. 479
Histopathological changes and clinical responses of Buruli ulcer plaque lesions during chemotherapy: a role for surgical removal of necrotic tissue? 480
Phase change material for thermotherapy of Buruli ulcer: a prospective observational single centre proof-of-principle trial. 480
Mycobacterium kansasii 480
155 Mycosis fungoides 483
Evolving insights in the pathogenesis and therapy of cutaneous T-cell lymphoma (mycosis fungoides and Sézary syndrome). 483
Cutaneous lymphoma incidence patterns in the United States: a population-based study of 3884 cases. 483
Incidence of cutaneous T-cell lymphoma in the United States, 1973–2002. 483
Diagnosis and staging 483
Defining early mycosis fungoides. 483
Revisions to the staging and classification of mycosis fungoides and Sézary syndrome: a proposal of the International Society for Cutaneous Lymphomas (ISCL) and the cutaneous lymphoma task force of the European Organization of Research and Treatment of Cancer (EORTC). 483
Natural history 484
Survival outcomes and prognostic factors in mycosis fungoides/Sézary syndrome: validation of the revised International Society for Cutaneous Lymphomas/European Organisation for Research and Treatment of Cancer staging proposal. 484
Long-term outcomes of 1263 patients with mycosis fungoides and Sézary syndrome from 1982 to 2009. 484
Second lymphomas and other malignant neoplasms in patients with mycosis fungoides and Sézary syndrome: evidence from population-based and clinical cohorts. 484
Management strategies 484
Multidisciplinary care in the management of patients with cutaneous lymphoma: a perspective. 484
A look at the National Comprehensive Cancer Network guidelines for cutaneous lymphomas. 484
Specific investigations 485
Review of the treatment of mycosis fungoides and Sézary syndrome: a stage-based approach. 485
Clinical end points and response criteria in mycosis fungoides and Sézary syndrome: a consensus statement of the International Society for Cutaneous Lymphomas (ISCL), the United States Cutaneous Lymphoma Consortium (USCLC), and the Cutaneous Lymphoma Task Force of the European Organisation for Research and Treatment of Cancer (EORTC). 485
First-line therapies 485
Long-term follow-up of patients with early-stage cutaneous T-cell lymphoma who achieved complete remission with psoralen plus UV-A monotherapy. 485
Narrowband UVB and psoralen-UVA in the treatment of early-stage mycosis fungoides: a retrospective study. 485
Monochromatic excimer light (308 nm) in patch-stage IA mycosis fungoides. 486
Photodynamic therapy with methyl-aminolaevulinic acid for mycosis fungoides. 486
Treatment of patch and plaque stage mycosis fungoides with imiquimod 5% cream. 486
Treatment of early-stage mycosis fungoides with twice-weekly applications of mechlorethamine and topical corticosteroids: a prospective study. 486
Comparison of pegylated interferon α−2b plus psoralen PUVA versus standard interferon α−2a plus PUVA in patients with cutaneous T-cell lymphoma. 486
Sézary syndrome: immunopathogenesis, literature review of therapeutic options, and recommendations for therapy by the United States Cutaneous Lymphoma Consortium (USCLC). 487
High clinical response rate of Sézary syndrome to immunomodulatory therapies: prognostic markers of response. 487
Photopheresis in the treatment of cutaneous T-cell lymphoma: current status. 487
Predictors of response to extracorporeal photopheresis in advanced mycosis fungoides and Sézary syndrome. 487
Second-line therapies 487
Phase IIb multicenter trial of vorinostat in patients with persistent, progressive, or treatment refractory cutaneous T-cell lymphoma. 487
Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL). 487
Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma. 487
Phase II multi-institutional trial of the histone deacetylase inhibitor romidepsin as monotherapy for patients with CTCL. 487
Alemtuzumab for relapsed and refractory erythrodermic cutaneous T-cell lymphoma: a single institution experience from the Robert H. Lurie Comprehensive Cancer Center. 487
Low-dose intermittent alemtuzumab in the treatment of Sézary syndrome: clinical and immunologic findings in 14 patients. 488
Third-line therapies 488
Total skin electron beam and non-myeloablative allogeneic hematopoietic stem-cell transplantation in advanced mycosis fungoides and Sézary syndrome. 488
156 Myiasis 489
Management strategy 489
Specific investigations 489
Scanning electron microscopy studies of sensilla and other structures of adult Dermatobia hominis (L. Jr., 1781) (Diptera: Cuterebridae). 489
Molecular identification of two species of myiasis-causing Cuterebra by multiplex PCR and RFLP. 489
Case report: myiasis – the botfly boil. 489
Cutaneous myiasis. 489
Identification of subcutaneous myiasis using bedside emergency physician performed ultrasound. 489
First-line therapies 489
Surgical therapy 490
157 Myxoid cyst 491
Management strategy 491
Specific investigations 491
Benign tumors and pseudotumors of the nail: a novel application of sonography. 491
MR imaging of digital mucoid cysts. 491
First-line therapies 491
Myxoid cysts of the finger: treatment by liquid nitrogen spray cryosurgery. 491
Specific indications for cryosurgery of the nail unit. 491
A simple technique for managing digital mucous cysts. 491
Treatment of digital myxoid cysts with carbon dioxide laser vaporization. 491
Treatment of mucoid cysts of fingers and toes by injection of sclerosant. 492
Second-line therapies 492
Marginal osteophyte excision in treatment of mucous cysts. 492
Etiology and treatment of the so called mucous cyst of the finger. 492
Use of Wolfe graft for the treatment of mucous cysts. 492
Ganglion of the distal interphalangeal joint (myxoid cyst): therapy by identification and repair of the leak of joint fluid. 492
Skin excision and osteophyte removal is not required in the surgical treatment of digital myxoid cysts. 492
Third-line therapies 492
Treatment of digital myxoid cysts with infrared coagulation: a retrospective case series. 492
Treatment of myxoid cyst with flurandrenolone tape. 492
158 Necrobiosis lipoidica 493
Management strategy 493
Specific investigations 493
Squamous cell carcinoma arising in an area of long-standing necrobiosis lipoidica. 493
Carcinoma cuniculatum arising in necrobiosis lipoidica. 493
Unilateral necrobiosis lipoidica of the ischemic limb – a case report. 493
Dermatoscopy of early onset necrobiosis lipoidica. 493
First-line therapies 493
Necrobiosis lipoidica diabeticorum: association with background retinopathy, smoking, and proteinuria. A case controlled study. 493
Granuloma annulare and necrobiosis lipoidica treated by jet injector. 494
Treatment of psoriasis and other dermatoses with a single application of a corticosteroid left under a hydrocolloid occlusive dressing for a week. 494
Second-line therapies 494
Necrobiosis lipoidica: treatment with systemic corticosteroids. 494
Ulcerating necrobiosis lipoidica effectively treated with pentoxifylline. 494
Healing of necrobiotic ulcers with antiplatelet therapy. Correlation with plasma thromboxane levels. 494
Treatment of necrobiosis lipoidica with low-dose acetylsalicylic acid. A randomized double-blind trial. 494
A randomized double blind comparison of an aspirin dipyridamole combination versus a placebo in the treatment of necrobiosis lipoidica. 494
Necrobiosis lipoidica treated with ticlopidine. 494
High dose nicotinamide in the treatment of necrobiosis lipoidica. 494
Clofazimine – therapeutic alternative in necrobiosis lipoidica and granuloma annulare. 494
Topical PUVA treatment for necrobiosis lipoidica. 494
Successful treatment of chronic ulcerated necrobiosis lipoidica with 0.1% topical tacrolimus ointment. 494
Third-line therapies 494
Necrobiosis lipoidica treated with topical tretinoin. 495
Persistent ulcerated necrobiosis lipoidica responding to treatment with cyclosporine. 495
Minidose heparin therapy for vasculitis of atrophie blanche. 495
Necrobiosis lipoidica diabeticorum treated with chloroquine. 495
Successful treatment of ulcerated necrobiosis lipoidica with mycophenolate mofetil. 495
Infliximab: a promising new treatment option for ulcerated necrobiosis lipoidica. 495
Ulcerative necrobiosis lipoidica: is there a place for anti-TNFα treatment? 495
Clearance of necrobiosis lipoidica with fumaric acid esters. 495
Fumaric acid esters in necrobiosis lipoidica: results of a prospective noncontrolled study. 495
The management of hard-to-heal necrobiosis with Promo-gran. 495
Healing of chronic leg ulcers in diabetic necrobiosis lipoidica with local granulocyte–macrophage colony- stimulating factor treatment. 495
Becaplermin and necrobiosis lipoidicum diabeticorum: results of a case control pilot study. 495
Necrobiosis lipoidica diabeticorum: response to pentoxiphylline. 495
Successful treatment of necrobiosis lipoidica diabeticorum with photodynamic therapy. 495
Necrobiosis lipoidica diabeticorum treated with the pulsed dye laser. 496
The surgical treatment of necrobiosis lipoidica diabeticorum. 496
Thalidomide for the treatment of refractory necrobiosis lipoidica. 496
Treatment of ulcerated necrobiosis lipoidica with intravenous immunoglobulin and methylprednisolone. 496
Dramatic response of chronic ulcerating necrobiosis lipoidica to ultraviolet A1 phototherapy. 496
159 Necrolytic migratory erythema 497
Management strategy 497
Specific investigations 497
Medical management of pancreatic neuroendocrine tumors. 497
Necrolytic migratory erythema: clinicopathologic study of 13 cases. 498
Necrolytic migratory erythema without glucagonoma in patients with liver disease. 498
Glucagon cell adenomatosis: a new entity associated with necrolytic migratory erythema and glucagonoma syndrome. 498
First-line therapies 498
Diagnosis and surgical treatment of pancreatic endocrine tumors in 36 patients: a single-center report. 498
Treatment with the radiolabeled somatostatin analog [177 Lu-DOTA 0,Tyr3]octreotate: toxicity, efficacy, and survival. 498
Second-line therapies 498
Glucagonoma syndrome: survival 21 years with concurrent liver metastases. 498
Peripheral amino acid and fatty acid infusion for the treatment of necrolytic migratory erythema in the glucagonoma syndrome. 498
Third-line therapies 498
Fluorouracil, doxorubicin, and streptozocin in the treatment of patients with locally advanced and metastatic pancreatic endocrine carcinoma. 498
Therapeutic management of patients with gastroenteropancreatic neuroendocrine tumors. 498
Sunitinib malate for the treatment of pancreatic neuroendocrine tumors. 498
Everolimus for advanced pancreatic neuroendocrine tumors. 498
Metastatic glucagonoma: treatment with liver transplantation. 498
160 Nephrogenic systemic fibrosis 499
Management strategy 499
FDA Drug Safety Communication: New warnings for using gadolinium-based contrast agents in patients with kidney dysfunction. 499
Specific investigations 499
Nephrogenic systemic fibrosis: clinicopathological definition and workup recommendations. 499
First-line therapies 499
Treatment of nephrogenic systemic fibrosis: limited options but hope for the future. 499
The outcome of patients with nephrogenic systemic fibrosis after successful kidney transplantation. 499
Clinical improvement of nephrogenic systemic fibrosis after kidney transplantation. 499
Renal transplantation for nephrogenic systemic fibrosis: a case report and review of literature. 499
Rehabilitation in nephrogenic systemic fibrosis. 499
Second-line therapies 499
Extracorporeal photopheresis improves nephrogenic fibrosing dermopathy/nephrogenic systemic fibrosis: three case reports and review of literature. 500
161 Neurofibromatosis, type 1 501
Management strategy 501
Specific investigations 502
Clinical and genetic aspects of neurofibromatosis 1. 502
Neurofibromatosis type I revisited. 502
Neurofibromatosis 1. 502
First-line therapies 502
The role of surgery in children with neurofibromatosis. 502
The megasession technique for excision of multiple neurofibromas. 502
Successful treatment of multiple cutaneous neurofibromas using a combination of shave excision and laser photothermocoagulation with a 1444-nm neodymium-doped yttrium aluminum garnet laser. 502
Malignant peripheral nerve sheath tumor: molecular pathogenesis and current management considerations. 502
Second-line therapies 502
A controlled multiphase trial of ketotifen to minimize neurofibroma-associated pain and itching. 502
Early outcomes for malignant peripheral nerve sheath tumor treated with chemotherapy. 503
Response of NF1-related plexiform neurofibroma to high-dose carboplatin. 503
Third-line and future therapies 503
Back to the future: Proceedings from the 2010 NF Conference. 503
Neurofibromatosis 2011: a report of the Children’s Tumor Foundation Annual Meeting. 503
Preclinical testing of sorafenib and RAD001 in the Nf(flox/flox)/DhhCre mouse model of plexiform neurofibroma using magnetic resonance imaging. 503
Tamoxifen inhibits malignant peripheral nerve sheath tumor growth in an estrogen-receptor independent manner. 503
Effect of simvastatin on cognitive functioning in children with neurofibromatosis type 1: a randomized controlled trial. 503
Lovastatin as treatment for neurocognitive defecits in neurofibromatosis type 1: phase 1 study. 503
Induction of apoptosis in neurofibromatosis type 1 malignant peripheral nerve sheath tumor cell lines by a combination of novel farnesyl transferase inhibitors and lovastatin. 503
Antisense therapeutics for neurofibromatosis type 1 caused by deep intronic mutations. 503
Phase II trial of pirfenidone in adults with neurofibromatosis type 1. 503
Radiofrequency in the treatment of craniofacial plexiform neurofibromatosis: a pilot study. 503
162 Nevoid basal cell carcinoma syndrome 504
Management strategy 504
Specific investigations 504
Radiologic images in dermatology: nevoid basal cell carcinoma syndrome. 504
Nevoid basal cell carcinoma syndrome (Gorlin syndrome). 504
A novel polymorphism in the PTC gene allows easy identification of allelic loss in basal cell nevus syndrome lesions. 504
How to diagnose nonpigmented skin tumors: a review of vascular structures seen with dermoscopy: part II. Nonmelanocytic skin tumors. 504
First-line therapies 504
Assessment and surgical treatment of basal cell skin cancer. 504
Guidelines for the management of BCC. 504
The nevoid basal cell carcinoma syndrome: sensitivity to the ultraviolet and x-ray irradiation. 505
Chemoprevention of basal cell carcinoma with isotretinoin. 505
Effectiveness of isotretinoin in preventing the appearance of basal cell carcinomas in basal cell nevus syndrome. 505
Skin cancer chemoprevention with systemic retinoids: an adjunct in the management of selected high-risk patients. 505
Systemic retinoids in chemoprevention of non-melanoma skin cancer. 505
A randomized, double-blind, placebo-controlled phase 3 skin cancer prevention study of α-difluoromethylornithine in subjects with previous history of skin cancer. 505
Basal cell carcinoma chemoprevention with nonsteroidal anti-inflammatory drugs in genetically predisposed PTCH1+/− humans and mice. 505
Nonsurgical innovations in the treatment of nonmelanoma skin cancer. 505
Second-line therapies 505
Combined curettage and excision: a treatment method for primary basal cell carcinoma. 505
Third-line therapies 505
Treatment of Gorlin syndrome (nevoid basal cell carcinoma syndrome) with methylaminolevulinate photodynamic therapy in seven patients, including two children: interest of tumescent anesthesia for pain control in children. 505
δ-Aminolevulinic acid and blue light photodynamic therapy for treatment of multiple basal cell carcinomas in two patients with nevoid basal cell carcinoma syndrome. 505
Treatment of diffuse basal cell carcinomas and basaloid follicular hamartomas in nevoid basal cell carcinoma syndrome by wide-area 5-aminolevulinic acid photodynamic therapy. 506
Guidelines on the use of photodynamic therapy for nonmelanoma skin cancer: an international consensus. 506
Efficacy of photodynamic therapy as a treatment for Gorlin syndrome-related basal cell carcinomas. 506
Imiquimod 5% cream for the treatment of superficial basal cell carcinomas: results from two phase III, randomized, vehicle-controlled studies. 506
Topical imiquimod or fluorouracil therapy for basal and squamous cell carcinoma: a systematic review. 506
The use of imiquimod 5% cream for the treatment of basal cell carcinoma as observed in Gorlin’s syndrome. 506
Cryosurgery for cutaneous malignancy: an update. 506
Cryosurgery and topical fluorouracil: a treatment method for widespread basal cell epithelioma in basal cell nevus syndrome. 506
Nonsurgical innovations in the treatment of nonmelanoma skin cancer. 506
Nonsurgical treatment of basal cell carcinomas with intralesional 5-fluorouracil/epinephrine injectable gel. 506
Gorlin syndrome: the role of the carbon dioxide laser in patient management. 506
Microscopically controlled surgical excision combined with ultrapulse CO2 vaporization in the management of a patient with the nevoid basal cell carcinoma syndrome. 506
Can the carbon dioxide laser completely ablate basal cell carcinomas? A histological study. 506
Full-face carbon dioxide laser resurfacing in the management of a patient with the nevoid basal cell carcinoma syndrome. 506
Ultrapulse CO2 used for the successful treatment of basal cell carcinomas found in patients with basal cell nevus syndrome. 506
The efficacy of facial skin cancer treatment with high-energy pulsed neodymium and Nd : YAG lasers. 506
Pulsed dye laser as a novel non-surgical treatment for basal cell carcinomas: response and follow up 12–21 months after treatment. 507
Single treatment of non-melanoma skin cancers using a pulsed-dye laser with stacked pulses. 507
755nm alexandrite laser for the reduction of tumor burden in basal cell nevus syndrome. 507
Intralesional agents in the management of cutaneous malignancy: a review. 507
Intralesional bleomycin-mediated electrochemotherapy in 20 patients with basal cell carcinoma. 507
Treatment and prevention of basal cell carcinoma with oral isotretinoin. 507
Effect of perilesional injections of PEG-interleukin-2 on basal cell carcinoma. 507
Nevoid basal cell carcinoma syndrome successfully treated with trichloroacetic acid and phenol peeling. 507
Widespread basal cell carcinoma of the scalp treated by dermabrasion. 507
Successful treatment of an intractable case of hereditary basal cell carcinoma syndrome with paclitaxel. 507
Novel approach to Gorlin syndrome: a patient treated with oral capecitabine. 507
Treatment for locally advanced or metastatic disease 507
Inhibition of the hedgehog pathway in advanced basal-cell carcinoma. 507
Emerging treatments and signaling pathway inhibitors. 508
Efficacy and safety of vismodegib in advanced basal-cell carcinoma. 508
Advances in the treatment of basal cell carcinoma: Hedgehog inhibitors. 508
Inhibiting the hedgehog pathway in patients with the basal-cell nevus syndrome. 508
Resolution of odontogenic keratocysts of the jaw in basal cell nevus syndrome with GDC-0449. 508
Treatment of medulloblastoma with hedgehog pathway inhibitor GDC-0449. 508
163 Nevus sebaceus 509
Management strategy 509
Tumors arising in nevus sebaceus: a study of 596 cases. 509
Should nevus sebaceus of Jadassohn in children be excised? A study of 757 cases, and literature review. 509
Trichoblastoma is the most common neoplasm developed in nevus sebaceus of Jadassohn: a clinicopathologic study of a series of 155 cases. 509
Management of nevus sebaceous and the risk of basal cell carcinoma: an 18-year review. 509
Nevus sebaceous revisited. 509
Specific interventions 509
First-line therapies 509
Should naevus sebaceus be excised prophylactically? A clinical audit. 510
Second-line therapies 510
Photodynamic therapy for nevus sebaceus with topical delta-aminolevulinic acid. 510
Linear nevus sebaceus of Jadassohn treated with the carbon dioxide laser. 510
Topical photodynamic therapy for nevus sebaceous on the face. 510
164 Notalgia paresthetica 511
Management strategy 511
Specific investigations 511
Notalgia paresthetica. Case reports and histologic appraisal. 511
Investigation of spinal pathology in notalgia paresthetica. 511
Notalgia paresthetica associated with nerve root impingement. 511
First-line therapies 511
Successful treatment of notalgia paresthetica with topical capsaicin: vehicle-controlled, double-blind, crossover study. 511
Notalgia paraesthetica – report of three cases and their treatment. 511
Second-line therapies 511
Cutaneous field stimulation (CFS) in treatment of severe localized itch. 511
Transcutaneous electrical nerve stimulation offers partial relief in notalgia paresthetica patients with a relevant spinal pathology. 512
Gabapentin treatment for notalgia paresthetica, a common isolated peripheral sensory neuropathy. 512
Open pilot study on oxcarbazepine for the treatment of notalgia paresthetica. 512
Third-line therapies 512
Notalgia paresthetica: clinical, physiopathological and therapeutic aspects. A study of 12 cases. 512
Botulinum toxin type A for neuropathic itch. 512
Neurogenic pruritus: an unrecognised problem? A retrospective case series of treatment by acupuncture. 512
Successful treatment of notalgia paresthetica with a paravertebral local anesthetic block. 512
165 Onchocerciasis 513
Management strategy 513
Treatment of individuals outside of endemic areas 513
Treatment of individuals within endemic areas 513
Mass treatment programs 513
Specific investigations 513
First-line therapies 514
The effects of ivermectin on onchocercal skin disease and severe itching: results of a multicentre trial. 514
The African Programme for Onchocerciasis Control: impact on onchocercal skin disease. 514
A trial of a three-dose regimen of ivermectin for the treatment of patients with onchocerciasis in the UK. 514
Ivermectin in the treatment of onchocerciasis in Britain. 514
Effects of standard and high doses of ivermectin on adult worms of Onchocerca volvulus: a randomised controlled trial. 514
An investigation of persistent microfilaridermias despite multiple treatments with ivermectin, in two onchocerciasis-endemic foci in Ghana. 514
Endosymbiotic bacteria in worms as targets for a novel chemotherapy in filariasis. 514
Depletion of Wolbachia endobacteria in Onchocerca volvulus by doxycycline and microfilaridermia after ivermectin treatment. 515
Wolbachia endobacteria depletion by doxycycline as antifilarial therapy has macrofilaricidal activity in onchocerciasis: a randomized placebo-controlled study. 515
Efficacy of 5-week doxycycline treatment on adult Onchocerca volvulus. 515
Macrofilaricidal activity after doxycycline only treatment of Onchocerca volvulus in an area of Loa loa co-endemicity: a randomized controlled trial. 515
Long term impact of large scale community-directed delivery of doxycycline for the treatment of onchocerciasis. 515
Second-line therapies 515
Albendazole in the treatment of onchocerciasis: double-blind clinical trial in Venezuela. 515
The co-administration of ivermectin and albendazole – safety, pharmacokinetics and efficacy against Onchocerca volvulus. 515
Other therapies 515
Thirty-month follow-up of sub-optimal responders to multiple treatments with ivermectin, in two onchocerciasis-endemic foci in Ghana. 515
WHO researchers start trial on a new drug for river blindness. 515
166 Oral lichen planus 516
Management strategy 516
Specific investigations 516
Direct immunofluorescence in oral lichen planus and oral lichenoid reactions. 516
Oral lichen planus and malignant transformation: a longitudinal cohort study. 516
Course of oral lichen planus: a retrospective study of 808 northern Italian patients. 517
Association between oral lichenoid reactions and amalgam restorations. 517
First-line therapies 517
Systemic and topical corticosteroid treatment of oral lichen planus: a comparative study with long-term follow-up. 517
Short-term clinical evaluation of intralesional triamcinolone acetonide injection for ulcerative oral lichen planus. 517
Second-line therapies 517
A comparative treatment study of topical tacrolimus and clobetasol in oral lichen planus. 517
Long-term efficacy and safety of topical tacrolimus in the management of ulcerative/erosive oral lichen planus. 517
Randomized trial of pimecrolimus cream versus triamcinolone acetonide paste in the treatment of oral lichen planus. 517
Pimecrolimus 1% cream for oral erosive lichen planus: a 6-week randomized, double-blind, vehicle-controlled study with a 6-week open-label extension to assess efficacy and safety. 517
Cyclosporine vs. clobetasol in the topical management of atrophic and erosive oral lichen planus: a double-blind, randomized controlled trial. 517
Oral lichen planus: a case series with emphasis on therapy. 517
Successful treatment of oral erosive lichen planus with mycophenolate mofetil. 517
A prospective study of findings and management in 214 patients with oral lichen planus. 517
Hydroxychloroquine sulfate (Plaquenil) improves oral lichen planus: an open trial. 517
Adalimumab in the management of cutaneous and oral lichen planus. 517
Etanercept for the management of oral lichen planus. 518
Levamisole monotherapy for oral lichen planus. 518
Third-line therapies 518
Topical tretinoin therapy and oral lichen planus. 518
Treatment of lichen planus with acitretin: a double-blind, placebo-controlled study in 65 patients. 518
Severe lichen planus clears with very low-dose cyclosporine. 518
Effective treatment of oral erosive lichen planus with thalidomide. 518
Efficacy of purslane in the treatment of oral lichen planus. 518
High-dose curcuminoids are efficacious in the reduction in symptoms and signs of oral lichen planus. 518
Lycopene in the management of oral lichen planus: a placebo-controlled study. 518
Efficacy of topical Aloe vera in patients with oral lichen planus: a randomized double-blind study. 518
Effect of low-level laser irradiation on unresponsive oral lichen planus: early preliminary results in 13 patients. 518
New clinical approach for use of Er : YAG laser in the surgical treatment of oral lichen planus: a report of two cases. 518
A comparative pilot study of low intensity laser versus topical corticosteroids in the treatment of erosive-atrophic oral lichen planus. 518
167 Orf 519
Management strategy 519
Specific investigations 519
The structure of the orf virus. 519
168 Palmoplantar keratoderma 521
Management strategy 521
Specific investigations 521
An epidemiologic investigation of dermatologic fungus infections in the northernmost county of Sweden (Norbotten) 1977–81. 521
Hereditary palmoplantar keratoderma and dermatophytosis in the northernmost county of Sweden (Norbotten). 522
Palmoplantar keratoderma in association with myxoedema. 522
Severe palmar keratoderma with myxoedema. 522
First-line therapies 522
Alleviation of the plantar discomfort caused by pachyonychia congenita with topical applications of aluminum chloride and salicylic acid ointments. 522
Vitamin A acid in the treatment of palmoplantar keratoderma. 522
Topical treatment of keratosis palmaris et plantaris with tretinoin. 522
Second-line therapies 522
The treatment of keratosis palmaris et plantaris with isotretinoin. A multicenter study. 522
Acitretin in the treatment of severe disorders of keratinisation. Results of an open study. 522
A controlled study of comparative efficacy of oral retinoids and topical betamethasone/salicylic acid for chronic hyperkeratotic palmoplantar dermatitis. 522
Acitretin in the treatment of mal de Meleda. 522
Keratoderma climactericum (Haxthausen’s disease), clinical and laboratory findings and etretinate treatment in 10 patients. 522
Mutilating palmoplantar keratoderma successfully treated with etretinate. 522
Third-line therapies 522
Plastic surgery in the management of palmoplantar keratoderma (palmoplantar neoplasty). 523
Palmoplantar keratoderma and skin grafting: postsurgical long-term follow-up of two cases with Olmsted syndrome. 523
Surgical correction of pseudo-ainhum in Vohwinkel syndrome. 523
Surgical correction of hyperkeratosis in the Papillon–Lefèvre syndrome. 523
Topical calcipotriol in the treatment of epidermolytic palmoplantar keratoderma of Vorner. 523
Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinisation. Results of a randomized, double blind vehicle-controlled, right/left comparative study. 523
Improvement of palmoplantar keratoderma of nonhereditary type (eczema tyloticum) after oral administration of 1 alpha 25-dihydroxyvitamin D3. 523
Oral psoralen photochemotherapy (PUVA) of hyperkeratotic dermatitis of the palms. 523
Dermabrasion of the hyperkeratotic foot. 523
Methods and effectiveness of surgical treatment of limited hyperkeratosis with CO2 laser. 523
Dietary management of oculocutaneous tyrosinemia in an 11 year old child. 523
169 Palmoplantar pustulosis 524
Management strategy 524
Specific investigations 524
Management of palmoplantar pustulosis: do we need to change? 524
Palmoplantar pustulosis associated with gastric Helicobacter pylori infection. 524
Thyroid disease in pustulosis palmoplantaris. 524
Osteoarticular manifestations of pustulosis palmaris et plantaris and of psoriasis: two distinct entities. 524
Skeletal involvement in pustulosis palmo-plantaris with special reference to the sterno-costo-clavicular joints. 524
SAPHO syndrome: a long-term follow-up study of 120 cases. 524
Women with palmoplantar pustulosis have disturbed calcium homeostasis and a high prevalence of diabetes mellitus and psychiatric disorders: a case-control study. 525
Palmoplantar pustulosis and gluten sensitivity: a study of serum antibodies against gliadin and tissue transglutaminase, the duodenal mucosa and effects of gluten-free diet. 525
First-line therapies 525
Interventions for chronic palmoplantar pustulosis. 525
A hydrocolloid occlusive dressing plus triamcinolone acetonide cream is superior to clobetasol cream in palmo-plantar pustulosis. 525
Second-line therapies 525
Double-blind placebo-controlled study of long-term low-dose cyclosporine in the treatment of palmoplantar pustulosis. 525
Pustulosis palmaris et plantaris treated with methotrexate. 525
Efficacy of fumaric acid ester monotherapy in psoriasis pustulosa palmoplantaris. 525
Efficacy of excimer light therapy (308 nm) for palmoplantar pustulosis with the induction of circulating regulatory T cells. 525
Third-line therapies 525
Psoriasis and palmoplantar pustulosis associated with tumor necrosis factor-α inhibitors: the Mayo Clinic experience, 1998 to 2010. 525
Open label trial of alefacept in palmoplantar pustular psoriasis. 525
Ustekinumab in the treatment of palmoplantar pustulosis. 525
Oral liarozole in the treatment of palmoplantar pustular psoriasis: a randomized, double-blind, placebo-controlled study. 525
170 Panniculitis 526
Management strategy 526
Specific investigations 527
Lupus panniculitis 528
First-line therapies 528
Connective tissue panniculitis: lupus panniculitis, dermatomyositis, morphea/scleroderma. 528
Systemic lupus erythematosus presenting as panniculitis (lupus profundus). 528
Connective tissue panniculitis. 528
Lupus erythematosus panniculitis (profundus). 528
Lupus erythematosus presenting as panniculitis. 528
Treatment of chronic discoid lupus erythematosus with intralesional triamcinolone. 528
Second-line therapies 528
Lupus erythematosus profundus treated with clobetasol propionate under a hydrocolloid dressing. 528
Lupus panniculitis treated by a combination therapy of hydroxychloroquine and quinacrine. 528
Third-line therapies 528
Intravenous immunoglobulin in lupus panniculitis. 528
A case of ‘refractory’ lupus erythematosus profundus responsive to rituximab [case report]. 528
Lupus erythematosus profundus. 529
Facets of lupus erythematosus: panniculitis responding to thalidomide. 529
Lupus erythematosus profundus with partial C4 deficiency responding to thalidomide. 529
The dynamism of cutaneous lupus erythematosus: mild discoid lupus erythematosus evolving into SLE and SCLE and treatment-resistant lupus panniculitis. 529
Lupus erythematosus profundus successfully treated with dapsone: review of the literature. 529
Nodular vasculitis 529
First-line therapies 529
Potassium iodide in the treatment of erythema nodosum and nodular vasculitis. 529
Treatment of erythema nodosum and nodular vasculitis with potassium iodide. 529
Successful treatment of erythema induratum of Bazin following rapid detection of mycobacterial DNA by polymerase chain reaction. 529
Erythema induratum of Bazin. 529
Diagnosis and treatment of erythema induratum (of Bazin). 529
Second-line therapies 529
Neutrophilic vascular reactions. 529
Chloroquine-induced remission of nodular panniculitis present for 15 years. 529
Cutaneous necrotizing vasculitis. 529
Third-line therapies 529
Nodular vasculitis (erythema induratum): treatment with auranofin. 529
Case reports: nodular vasculitis responsive to mycophenolate mofetil. 529
Pancreatic panniculitis 530
171 Papular urticaria 532
Specific investigations 532
Papular urticaria: a histopathologic study of 30 patients. 533
Immune responses to mosquito saliva in 14 individuals with acute systemic allergic reactions to mosquito bites. 533
Specific pattern of flea antigen recognition by IgG subclass and IgE during the progression of papular urticaria caused by flea bite. 533
First-line therapies 533
Papular urticaria in children. 533
Tropical rat mite dermatitis. 533
Flea infestation as a cause of papular urticaria. 533
Comparison of cetirizine, ebastine and loratadine in the treatment of immediate mosquito-bite allergy. 533
Levocetirizine for treatment of immediate and delayed mosquito bite reactions. 533
Bullous papular urticaria. 533
172 Paracoccidioidomycosis (South American blastomycosis) 535
Management strategy 535
Specific investigations 535
Paracoccidioidomycosis and AIDS: an overview. 536
Paracoccidioidomycosis in patients with human immunodeficiency virus: review of 12 cases observed in an endemic region in Brazil. 536
Pharmacological management of paracoccidioidomycosis. 536
Drugs for treating paracoccidioidomycosis. 536
Treatment options for paracoccidioidomycosis and new strategies investigated. 536
Paracoccidioidomycosis. 536
Central nervous system paracoccidioidomycosis: an overview. 536
First-line therapies 536
Treatment of paracoccidioidomycosis with itraconazole. 536
Randomized trial with itraconazole, ketoconazole and sulfadiazine in paracoccidioidomycosis. 536
Paracoccidioidomycosis in children: clinical presentation, follow-up and outcome. 537
Paracoccidioidomycosis: a clinical and epidemiological study of 422 cases observed in Mato Gross do Sul. 537
Clinical and serologic features of 47 patients with paracoccidioidomycosis treated by amphotericin B. 537
Paracoccidioidomycosis: a comparative study of the evolutionary serologic, clinical and radiologic results for patients treated with ketoconazole or amphotericin B plus sulfonamides. 537
Failure of amphotericin B colloidal dispersion in the treatment of paracoccidioidomycosis. 537
Second-line therapies 537
Treatment of paracoccidioidomycosis with ketoconazole: a three-year experience. 537
A Pan-American 5-year study of fluconazole therapy for deep mycoses in the immunocompetent host. Pan-American Study Group. 537
An open-label comparative pilot study of oral voriconazole and itraconazole for long-term treatment of paracoccidioidomycosis. 537
Chronic paracoccidioidomycosis in a female patient in Austria. 538
Paracoccidioidomycosis (South American blastomycosis) successfully treated with terbinafine: first case report. 538
173 Parapsoriasis 539
Management strategy 539
Specific investigations 539
Assessment of TCR-beta clonality in a diverse group of cutaneous T-cell infiltrates. 539
Clonal T cell receptor gamma-chain gene rearrangement by PCR-based GeneScan analysis in the skin and blood of patients with parapsoriasis and early-stage mycosis fungoides. 539
The role of immunohistochemical analysis in the diagnosis of parapsoriasis. 539
Small plaque parapsoriasis 539
First-line therapies 539
Narrowband UVB phototherapy for small plaque parapsoriasis. 539
Treatment of small plaque parapsoriasis with narrow-band (311 nm) ultraviolet B: a retrospective study. 539
Narrowband (311-nm) UV-B therapy for small plaque parapsoriasis and early-stage mycosis fungoides. 540
Treatment of parapsoriasis and mycosis fungoides: the role of psoralen and long-wave ultraviolet light A (PUVA). 540
174 Paronychia 542
Management strategy 542
Specific investigations 542
Anaerobic paronychia. 542
Chronic paronychia. Short review of 590 cases. 542
Role of foods in the pathogenesis of chronic paronychia. 543
First-line therapies 543
Paronychia: a mixed infection, microbiology and management. 543
Nail surgery and traumatic abnormalities. 543
Topical steroids versus systemic antifungals in the treatment of chronic paronychia: an open, randomized double-blind and double dummy study. 543
Efficacy and safety of tacrolimus ointment 0.1% vs. betamethasone 17-valerate 0.1% in the treatment of chronic paronychia: an unblinded randomized study. 543
The management of superficial candidiasis. 543
Diseases of the nails in infants and children: paronychia. 543
Retronychia: report of two cases. 543
Paronychia associated with antiretroviral therapy. 543
Doxycycline for the treatment of paronychia induced by the epidermal growth factor receptor inhibitor cetuximab. 543
Paronychia and pyogenic granuloma induced by new anticancer mTOR inhibitors. 543
Second-line therapies 543
Treatment of chronic paronychia. 543
Fungal and other infections. 544
Third-line therapies 544
Thumb paronychia treated with leeches. 544
Eponychial marsupialization and nail removal for surgical treatment of chronic paronychia. 544
Surgical treatment of recalcitrant chronic paronychia of the fingers. 544
How we treat paronychia. 544
175 Parvovirus infection 545
Management strategy 545
Specific investigations 546
Parvovirus B19. 546
The cutaneous manifestations of human parvovirus B19 infection. 546
First-line therapies 546
Human parvoviruses. 546
Second-line therapies 546
Human parvovirus infection: rheumatic manifestations, angioedema, C1 esterase inhibitor deficiency, ANA positivity and possible onset of systemic lupus erythematosus. 546
Parvoviruses and bone marrow failure. 547
Third-line therapies 547
Persistent B19 parvovirus infection in patients infected with human immunodeficiency virus type 1 (HIV-1): a treatable cause of anaemia in AIDS. 547
Intravenous immunoglobulins in autoimmune or parvovirus B19-mediated pure red cell aplasia. 547
Intravenous immunoglobulin treatment of four patients with juvenile polyarticular arthritis associated with persistent parvovirus B19 infection and antiphospholipid antibodies. 547
Mononeuropathy multiplex associated with acute parvovirus B19 infection: characteristics, treatment and outcome. 547
Stem cell transplantation in 6 children with parvovirus B19-induced severe aplastic anaemia or myelodysplastic syndrome. 547
Fetal morbidity and mortality after acute parvovirus B19 infection in pregnancy: prospective evaluation of 1018 cases. 547
Parvovirus B19 in pregnancy: prenatal diagnosis and management of fetal complications. 547
Resolution of chronic parvovirus B19 induced anemia, by use of highly active antiretroviral therapy in a patient with acquired immunodeficiency syndrome. 547
176 Pediculosis 548
Pediculosis capitis 548
Management strategy 548
Specific investigations 548
Louse comb versus direct visual examination for the diagnosis of head louse infestations. 548
Dermoscopy for diagnosis and treatment monitoring of pediculosis capitis. 548
First-line therapies 549
The clinical trials supporting benzyl alcohol lotion 5% (Ulesfia): a safe and effective topical treatment for head lice (pediculosis humanus capitis). 549
Pediculosis capitis: why prefer a solution to shampoo or spray? 549
Sklice [package insert]. 549
Therapy for head lice based on life cycle, resistance, and safety considerations. 549
Effectiveness of Ovide against malathion-resistant head lice. 549
Efficacy of a reduced application time of Ovide lotion (0.5% malathion) compared to Nix creme rinse (1% permethrin) for the treatment of head lice. 549
Increased frequency of the T929I and L932F mutations associated with knockdown resistance in permethrin-resistant populations of the human head louse, Pediculus capitis, from California, Florida and Texas. 549
Efficacy and safety of spinosad and permethrin creme rinses for pediculosis capitis (head lice). 549
Second–line therapies 549
A single application of crotamiton lotion in the treatment of patients with pediculosis capitis. 549
A randomised, assessor blind, parallel group comparative efficacy trial of three products for the treatment of head lice in children – melaleuca oil and lavender oil, pyrethrins and piperonyl butoxide, and a ‘suffocation’ product. 549
A randomized, assessor-blind, parallel-group, multicentre, phase IV comparative trial of a suffocant compared with malathion in the treatment of head lice in children. 550
Treatment of head louse infestation with 4% dimethicone lotion: randomised controlled equivalence trial. 550
A simple treatment for head lice: dry-on, suffocation-based pediculicide. 550
North American efficacy and safety of a novel pediculicide rinse, isopropyl myristate 50% (Resultz). 550
Single blind, randomised, comparative study of the Bug Buster kit and over the counter pediculicide treatments against head lice in the United Kingdom. 550
Third-line therapies 550
Treatment of pediculosis capitis with topical albendazole. 550
Home remedies to control head lice: assessment of home remedies to control the human head louse, Pediculus humanus capitis (Anoplura: Pediculidae). 550
Oral ivermectin versus malathion lotion for difficult-to-treat head lice. 550
Comparative in vitro pediculicidal efficacy of treatments in a resistant head lice population in the United States. 550
Lindane toxicity: a comprehensive review of the medical literature. 550
Head lice infestation: single drug versus combination therapy with one percent permethrin and trimethoprim/sulfamethoxazole. 550
Levamisole: a safe and economical weapon against pediculosis. 550
Pediculosis corporis 550
Management strategy 550
177 Pemphigus 552
Management strategy 552
Specific investigations 552
Making sense of antigens and antibodies in pemphigus. 552
Accuracy of indirect immunofluorescence testing in the diagnosis of paraneoplastic pemphigus. 552
First-line therapies 553
Pemphigus: a 20 year review of 107 patients treated with corticosteroids. 553
Successful treatment of pemphigus with bi-weekly one gram infusions of rituximab: a retrospective study of 47 patients. 553
Treatment of refractory pemphigus vulgaris with rituximab (anti-CD20 monoclonal antibody). 553
A single cycle of rituximab for the treatment of severe pemphigus. 553
Second-line therapies 554
Treatment of pemphigus vulgaris and foliaceus with mycophenolate mofetil. 554
Azathioprine in the treatment of pemphigus vulgaris. A long term follow-up. 554
A comparison of oral methylprednisolone plus azathioprine or mycophenolate mofetil for the treatment of pemphigus. 554
Randomized controlled open-label trial of four treatment regimens for pemphigus vulgaris. 554
High-dose intravenous immune globulin for the treatment of autoimmune blistering diseases. 554
Treatment of pemphigus with intravenous immunoglobulin. 554
Third-line therapies 555
Dexamethasone-cyclophosphamide pulse therapy for pemphigus. 555
Synchronization of plasmapheresis and pulse cyclophosphamide therapy in pemphigus vulgaris. 555
The use of chlorambucil with prednisone in the treatment of pemphigus. 555
Ineffectiveness of cyclosporine as an adjuvant to corticosteroids in the treatment of pemphigus. 555
178 Perforating dermatoses 556
Management strategy 556
Specific investigations 556
Reactive perforating collagenosis associated with diabetes mellitus. 556
Acquired perforating dermatosis: clinicopathological features in twenty-two cases. 556
First-line therapies 556
Familial reactive perforating collagenosis: a clinical, histopathological study of 10 cases. 557
Tazarotene is an effective therapy for elastosis perforans serpiginosa. 557
Acquired reactive collagen disease in the adult: successful treatment with UV-B light. 557
Treatment of acquired perforating dermatosis with narrowband ultraviolet B. 557
Second-line therapies 557
Acquired reactive perforating collagenosis: four patients with a giant variant treated with allopurinol. 557
Reactive perforating collagenosis: a condition that may be underdiagnosed. 557
Kyrle’s disease. Effectively treated with isotretinoin. 557
Reactive perforating collagenosis responsive to PUVA. 557
Third-line therapies 557
Successful treatment of acquired reactive perforating collagenosis with doxycycline. 557
Regression of skin lesions of Kyrle’s disease with metronidazole in a diabetic patient. 558
Regression of skin lesions of Kyrle’s disease with clindamycin: implications for an infectious component in the etiology of the disease. 558
Sirolimus-induced inflammatory papules with acquired reactive perforating collagenosis. 558
Imiquimod therapy for elastosis perforans serpiginosa. 558
A new treatment for acquired reactive perforating collagenosis. 558
Elastosis perforans serpignosa: treatment with liquid nitrogen cryotherapy and review of the literature. 558
Treatment of acquired perforating dermatosis with cantharidin. 558
Acquired perforating dermatosis successfully treated with photodynamic therapy. 558
Localized idiopathic elastosis perforans serpiginosa effectively treated by the coherent ultrapulse 5000C aesthetic laser. 558
Response of elastosis perforans serpiginosa to pulsed CO2, Er:YAG, and dye lasers. 558
Treatment of elastosis perforans serpiginosa with the pinhole method using a carbon dioxide laser. 558
Treatment of pruritus of reactive perforating collagenosis using transcutaneous electrical nerve stimulation. 558
179 Perioral dermatitis 559
Management strategy 559
Specific investigations 559
First-line treatment 559
Complications of topical hydrocortisone. 559
Perioral dermatitis: aetiology and treatment with tetracycline. 559
Perioral dermatitis in renal transplant recipients maintained on corticosteroids and immunosuppressive therapy. 559
Second-line treatments 559
Pimecrolimus cream (1%) efficacy in perioral dermatitis: results of a randomized, double-blind, vehicle-controlled study in 40 patients. 559
A randomized, double-blind, vehicle-controlled study of 1% pimecrolimus cream in adult patients with perioral dermatitis. 560
Topical tetracycline in the treatment of perioral dermatitis. 560
A topical erythromycin preparation and oral tetracycline for the treatment of perioral dermatitis: a placebo- controlled trial. 560
Topical therapy for perioral dermatitis. 560
Identical twins with perioral dermatitis. 560
Topical metronidazole in the treatment of perioral dermatitis. 560
Topical metronidazole gel (0.75%) for the treatment of perioral dermatitis in children. 560
Azelaic acid as a new treatment for perioral dermatitis: results from an open study. 560
Perioral dermatitis with histopathologic features of granulomatous rosacea: successful treatment with isotretinoin. 560
Perioral dermatitis successfully treated with topical adapalene. 560
Photodynamic therapy for perioral dermatitis. 560
180 Peutz–Jeghers syndrome 561
Management strategy 561
Specific investigations 561
Small bowel endoscopy and Peutz-Jeghers syndrome. 561
Peutz-Jeghers syndrome: a systematic review and recommendations for management. 561
Quality of life and psychological distress in patients with Peutz-Jeghers syndrome. 561
Genetics of the hamartomatous polyposis syndromes: a molecular review. 562
Peutz–Jeghers syndrome. 562
Further observations on LKB1/STK11 status and cancer risk in Peutz–Jeghers syndrome. 562
Peutz–Jeghers syndrome: genetic screening. 562
Peutz–Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4. 562
Harold Joseph Jeghers. Schwartz RA. 562
First-line therapies 562
Q-switched alexandrite laser treatment of oral labial lentigines in Chinese subjects with Peutz–Jeghers syndrome. 562
Q-switched ruby laser treatment of labial lentigos. 562
Successful treatment of mucosal melanosis of the lip with normal pulsed ruby laser. 562
Ruby laser therapy for labial lentigines in Peutz–Jeghers syndrome. 562
Q-switched ruby laser treatment of tattoos and benign pigmented lesions: a critical review. 562
Second-line therapies 562
Treatment of Peutz–Jeghers lentigines with the carbon dioxide laser. 562
Q-switched alexandrite laser in the treatment of pigmented macules in Laugier–Hunziker syndrome. 562
Treatment of pigmentation of the lips and oral mucosa in Peutz–Jeghers syndrome using ruby and argon lasers. 562
Treatment of facial lentigines in Peutz–Jeghers syndrome with intense pulsed light source. 563
Simple cryosurgical treatment of the oral melanotic macule. 563
Chemopreventive efficacy of rapamycin on Peutz - Jeghers syndrome in a mouse model. 563
Suppression of Peutz Jeghers polyposis by targeting mammalian target of rapamycin signaling. 563
181 Physical urticarias, aquagenic pruritus, and cholinergic pruritus 564
Physical urticarias 564
Management strategy 564
Pharmacologic 564
Non-pharmacologic 564
Specific investigations 564
EAACI/GA(2)LEN/EDF/WAO guideline: definition, classification and diagnosis of urticaria. 564
The definition and diagnostic testing of physical and cholinergic urticarias – EAACI/GA2LEN/EDF/UNEV consensus panel recommendations. 564
Cold urticaria syndromes: historical background, diagnostic classification, clinical and laboratory characteristics, pathogenesis and management. 564
Food-dependent exercise-induced anaphylaxis. 564
First-line therapies 565
Therapeutic effects of cetirizine in delayed pressure urticaria: clinicopathological findings. 565
High-dose desloratadine decreases wheal volume and improves cold provocation thresholds compared with standard–dose treatment in patients with acquired cold urticaria: a randomized, placebo-controlled, cross-over study. 565
Rupatadine and its effects on symptom control, stimulation time, and temperature thresholds in patients with acquired cold urticaria. 565
Second-line therapies 565
Symptomatic dermographism 565
In dermographic urticaria H2 receptor antagonists have a small but therapeutically irrelevant additional effect compared with H1 antagonists alone. 565
Narrow-band ultraviolet B phototherapy is beneficial in antihistamine-resistant symptomatic dermographism: a pilot study. 565
The effect of psoralen photochemotherapy (PUVA) on symptomatic dermographism. 565
Anti-immunoglobulin E treatment of patients with recalcitrant physical urticaria. 565
Cholinergic urticaria 565
Beneficial effects of danazol on symptoms and laboratory changes in cholinergic urticaria. 565
Severe cholinergic urticaria successfully treated with scopolamine butylbromide in addition to antihistamines. 566
Rapid desensitization with autologous sweat in cholinergic urticaria. 566
Successful treatment of cholinergic urticaria with anti-immunoglobulin E therapy. 566
Failure of omalizumab in cholinergic urticaria. 566
Cold urticaria 566
Cold urticaria: a clinico-therapeutic study in 30 patients, with special emphasis on cold desensitization. 566
Cold urticaria: tolerance induction with cold baths. 566
Improvement of cold urticaria by treatment with the leukotriene receptor antagonist montelukast. 566
Treatment of acquired cold urticaria with cetirizine and zafirlukast in combination. 566
Acquired cold urticaria: clinical picture and update on diagnosis and treatment. 566
Successful treatment of cold-induced urticaria/anaphylaxis with anti-IgE. 566
Anti-immunoglobulin E treatment of patients with recalcitrant physical urticaria. 566
Heat urticaria 566
Effective treatment of refractory severe heat urticaria with omalizumab. 567
182 Pinta and yaws 571
Management strategy 571
Specific investigations 572
A description of the yaws infection and prevention conditions in the health district of Adzope. 572
The endemic treponematoses. 572
Histopathological aspects of tertiary pinta. 572
The sequence of the acidic repeat protein (arp) gene differentiates venereal from nonvenereal Treponema pallidum subspecies, and the gene has evolved under strong positive selection in the subspecies that causes syphilis. 572
Genetic diversity in Treponema pallidum: implications for pathogenesis, evolution and molecular diagnostics of syphilis and yaws. 572
First-line therapies 572
Treponemal infections. 572
Treatment of pinta with antibiotics. 572
Nonvenereal treponematoses in tropical countries. 572
Failure of penicillin treatment of yaws on Karkar Island, Papua New Guinea. 572
Efficacy of a targeted, oral penicillin-based yaws control program among children living in rural South America. 572
Overview of endemic treponematoses. 572
Second-line therapies 572
Therapy for nonvenereal treponematosis. Review of the efficacy of penicillin and consideration of alternatives. 572
Nonvenereal treponematoses: yaws, endemic syphilis, and pinta. 573
Endemic treponematosis: review and update. 573
Yaws eradication: past efforts and future perspectives. 573
182 Pitted and ringed keratolysis (keratolysis plantare sulcatum) 574
Management strategy 574
Specific investigations 574
Pitted keratolysis. The role of Micrococcus sedentarius. 575
Isolation and characterization of micrococci from human skin, including two new species: Micrococcus lylae and Micrococcus kristinae. 575
First-line therapies 575
Isolation of Kytococcus sedentarius from a case of pitted keratolysis. 575
Coexistent erythrasma, trichomycosis axillaris, and pitted keratolysis: an overlooked corynebacterial triad? 575
Pitted and ringed keratolysis. A review and update. 575
Pitted keratolysis of the palm arising after herpes zoster [Letter]. 575
Formaldehyde treatment for pitted keratolysis. 575
Second-line therapies 575
Mupirocin ointment for symptomatic pitted keratolysis [Letter]. 575
P1606 Kytococcus sedentarius nail infection. 575
Pitted keratolysis: A new form of treatment [Letter]. 575
Road rash with a rotten odor. 575
The use of a clindamycin 1% - benzoyl peroxide 5% topical gel in the treatment of pitted keratolysis: a novel therapy. 575
Comparative study of benzoyl peroxide versus clindamycin phosphate in treatment of pitted keratolysis. 575
Pitted keratolysis: a clinicopathologic review. 575
Painful, plaque-like, pitted keratolysis occurring in childhood. 576
Ultrastructure of pitted keratolysis. 576
Third-line therapies 576
Pitted keratolysis: forme fruste old treatments [Letter]. 576
Pitted keratolysis: forme fruste. A review and new therapies. 576
Hyperhidrosis: treatment with glutaraldehyde. 576
Glutaraldehyde solution. 576
Keratolysis plantare sulcatum. 576
Symptomatic pitted keratolysis. 576
Pitted keratolysis. 576
Plantar hyperhidrosis and pitted keratolysis treated with botulinum toxin injection. 576
184 Pityriasis lichenoides chronica 577
Pityriasis lichenoides chronica: stratification by molecular and phenotypic profile. 577
Management strategy 577
Specific investigations 577
The relationship between toxoplasmosis and pityriasis lichenoides chronica. 577
Pityriasis lichenoides et varioliformis acuta and pityriasis lichenoides chronica: comparison of lesional T-cell subsets and investigation of viral associations. 577
First-line therapies 577
Comparative studies of treatments for pityriasis lichenoides. 577
UVB therapy of pityriasis lichenoides. 578
Narrowband UVB (311 nm, TL01) phototherapy for pityriasis lichenoides. 578
UV-B phototherapy for pityriasis lichenoides. 578
Phototherapy of pityriasis lichenoides. 578
PUVA therapy of pityriasis lichenoides chronica. 578
Comparison of the therapeutic effects of narrowband UVB vs PUVA in patients with pityriasis lichenoides. 578
Second-line therapies 578
Pityriasis lichenoides: the differences between children and adults. 578
Pityriasis lichenoides in childhood: a retrospective review of 124 patients. 578
Childhood pityriasis lichenoides and oral erythromycin. 578
Tetracycline for the treatment of pityriasis lichenoides. 578
Third-line therapies 578
Methotrexate treatment of pityriasis lichenoides and lymphomatoid papulosis. 578
Successful treatment of pityriasis lichenoides chronica with acitretin. 578
Photochemotherapy for pityriasis lichenoides: 3 cases. 578
Cyclosporine in dermatology. 578
Medium-dose ultraviolet A1 therapy for pityriasis lichenoides varioliformis acuta and pityriasis lichenoides chronica. 579
Role of bromelain in the treatment of patients with pityriasis lichenoides chronica. 579
Refractory pityriasis lichenoides chronica successfully treated with topical tacrolimus. 579
Successful treatment of pityriasis lichenoides with topical tacrolimus. 579
Pityriasis lichenoides chronica: good response to photodynamic therapy. 579
Etanercept in therapy multiresistant overlapping pityriasis lichenoides. 579
185 Pityriasis lichenoides et varioliformis acuta 580
Management strategy 580
Specific investigations 580
Pityriasis lichenoides: a cytotoxic T-cell-mediated skin disorder. Evidence of human parvovirus B19 DNA in nine cases. 580
Pityriasis lichenoides et varioliformis acuta and group-A beta hemolytic streptococcal infection. 580
Pityriasis lichenoides and acquired toxoplasmosis. 580
First-line therapies 580
Pityriasis lichenoides in childhood: a retrospective review of 124 patients. 580
Pityriasis lichenoides in children: therapeutic response to erythromycin. 580
Mucha Habermann’s disease in children: treatment with erythromycin. 581
Second-line therapies 581
Pityriasis lichenoides in children: a long term follow-up of eighty-nine cases. 581
Comparative studies of treatment for pityriasis lichenoides. 581
Narrowband UVB (311 nm, TL01) phototherapy for pityriasis lichenoides. 581
Erprobung von PUVA bei verscheidenen Dermatosen. 581
Experience with UVB phototherapy in children. 581
Photochemotherapy for pityriasis lichenoides. 581
Third-line therapies 581
Methotrexate for the treatment of Mucha–Habermann disease. 581
Mucha Habermann’s disease. 581
Zur Behandlung der Pityriasis lichenoides et varioliformis acuta mit Methotrexat. 581
Febrile ulceronecrotic Mucha–Habermann’s disease managed with methylprednisolone semipulse and subsequent methotrexate therapies. 581
Successful long-term use of cyclosporin A in HIV-induced pityriasis lichenoides chronica. 581
Febrile ulceronecrotic Mucha–Habermann’s disease and its successful therapy with DDS. 582
Transition of pityriasis lichenoides et varioliformis acuta to febrile ulceronecrotic Mucha–Habermann disease is associated with elevated serum tumour necrosis factor-alpha. 582
High dose immunoglobulins and extracorporeal photochemotherapy in the treatment of febrile ulceronecrotic Mucha–Habermann disease. 582
Successful association in the treatment of pityriasis lichenoides et varioliformis acuta. 582
186 Pityriasis rosea 583
Management strategy 583
Specific investigations 583
First-line therapies 583
Pityriasis rosea update: 1986. 583
Interventions for pityriasis rosea. 583
Second-line therapies 583
Treatment of pityriasis rosea with UV radiation. 583
UVB phototherapy for pityriasis rosea: a bilateral comparison study. 583
UVB phototherapy for pityriasis rosea. 584
Low-dose ultraviolet A1 phototherapy for treating pityriasis rosea. 584
Third-line therapies 584
One year review of pityriasis rosea at the National Skin Centre, Singapore. 584
Pityriasis rosea: exacerbation with corticosteroid treatment. 584
Erythromycin in pityriasis rosea: a double-blind, placebo-controlled clinical trial. 584
Vesicular pityriasis rosea: response to erythromycin treatment. 584
The comparison between the efficacy of high dose acyclovir and erythromycin on the period and signs of pityriasis rosea. 584
Use of high-dose acyclovir in pityriasis rosea. 584
Low dose acyclovir may be an effective treatment against pityriasis rosea: a random investigator-blind clinical trial on 64 patients. 584
Antivirals for pityriasis rosea. 584
Dapsone treatment in a case of vesicular pityriasis rosea. 584
187 Pityriasis rubra pilaris 585
Management strategy 585
Specific investigations 585
First-line therapies 585
Treatment of classic pityriasis rubra pilaris. 585
Pityriasis rubra pilaris: a review of treatment and diagnosis. 585
Pityriasis rubra pilaris. 585
Second-line therapies 585
A systematic review of the literature on the treatment of pityriasis rubra pilaris type I with TNF-alpha antagonists. 586
Successful treatment of pityriasis rubra pilaris (type 1) under combination of infliximab and methotrexate. 586
HIV-associated pityriasis rubra pilaris : response to triple anti-retroviral therapy. 586
Third-line therapies 586
Pityriasis rubra pilaris treated with acitretin and narrow-band UVB (Re-TL-01). 586
Combination ultraviolet A1 radiation and acitretin therapy as a treatment option for pityriasis rubra pilaris. 586
Photoaggravated pityriasis rubra pilaris. 586
Extracorporeal photochemotherapy for the treatment of erythrodermic pityriasis rubra pilaris. 586
Extracorporeal photochemotherapy for the treatment of exanthemic pityriasis rubra pilaris. 586
Type II adult-onset pityriasis rubra pilaris successfully treated with intravenous immunoglobulin. 586
Successful treatment of type I pityriasis rubra pilaris with ustekinumab. 586
Treatment of pityriasis rubra pilaris with ustekinumab. 586
Fumaric acid esters: a new treatment modality for pityriasis rubra pilaris. 586
188 Polycystic ovary syndrome 587
Management strategy 587
Specific investigations 587
Impaired glucose tolerance, type 2 diabetes and metabolic syndrome in polycystic ovary syndrome: a systematic review and meta-analysis. 587
Meta-analysis of cardiovascular disease risk markers in women with polycystic ovary syndrome. 587
Polycystic ovary syndrome increases the risk of endometrial cancer in women aged less than 50 years: an Australian case-control study. 587
Polycystic ovary syndrome and mental health: a review. 587
First-line therapies 587
Lifestyle changes in women with polycystic ovary syndrome. 588
Current approches to the diagnosis and treatment of polycystic ovarian syndrome in youth. 588
Treatment of hirsutism and acne in hyperandrogenism. 588
Topical eflornithine. 588
A randomised, split-face comparison of facial hair removal with the alexandrite laser and intense pulsed light system. 588
Second-line therapies 588
Combined oral contraceptive pills for treatment of acne. 588
Cyproterone acetate or drospirenone containing combined oral contraceptives plus spironolactone or cyproterone acetate for hirsutism: randomized comparison of three regimens. 588
Spironolactone versus placebo or in combination with steroids for hirsutism and/or acne. 588
Comparison of spironolactone, flutamide, and finasteride efficacy in the treatment of hirsutism: a randomized, double blind, placebo-controlled trial. 588
Insulin-sensitising drugs versus the combined oral contraceptive pill for hirsutism, acne and risk of diabetes, cardiovascular disease, and endometrial cancer in polycystic ovary syndrome (review). 588
Metformin therapy in women with polycystic ovary syndrome. 588
Third-line therapies 588
When should an insulin sensitizing agent be used in the treatment of polycystic ovary syndrome? 588
189 Polymorphic light eruption 589
Management strategy 589
Specific investigations 589
Marked papillary dermal edema – an unreliable discriminator between polymorphous light eruption and lupus erythematosus or dermatomyositis. 589
Clinical and therapeutic aspects of polymorphous light eruption. 589
An optimal method for experimental provocation of polymorphic light eruption. 589
The prevalence of antinuclear antibodies in patients with apparent polymorphic light eruption. 590
First-line therapies 590
A new ecamsule-containing SPF 40 sunscreen cream for the prevention of polymorphous light eruption: a double-blind, randomized, controlled study in maximized outdoor conditions. 590
Textiles and sun protection. 590
Second-line therapies 590
UVB phototherapy and photochemotherapy (PUVA) in the treatment of polymorphic light eruption and solar urticaria. 590
A comparison of narrowband (TL-01) and photochemotherapy (PUVA) in the management of polymorphic light eruption. 590
Third-line therapies 590
Efficacy of short-course oral prednisolone in polymorphic light eruption: a randomized controlled trial. 590
Hydroxychloroquine in polymorphic light eruption: a controlled trial with drug and visual sensitivity monitoring. 590
Comparison of PUVA and beta-carotene in the treatment of polymorphous light eruption. 590
Treatment of polymorphous light eruption with nicotinamide: a pilot study. 590
Successful treatment of severe polymorphous light eruption with azathioprine. 590
Prophylactic short-term use of cyclosporine in refractory polymorphic light eruption. 591
Polymorphous light eruption (PLE) and a new potent antioxidant and UVA-protective formulation as prophylaxis. 591
Topical liposomal DNA-repair enzymes in polymorpghic light eruption. 591
Photoprotective activity of oral Polypodium leucotomos extract in 25 patients with idiopathic photodermatoses. 591
LED photoprevention: reduced MED response following multiple LED exposures. 591
190 Pompholyx 592
Management strategy 592
Specific investigations 592
Pompholyx eczema as a manifestation of HIV infection, response to antiretroviral therapy. 592
Pompholyx and eczematous reactions associated with intravenous immunoglobulin therapy. 592
A 3-year causative study of pompholyx in 120 patients. 592
Role of contact allergens in pompholyx. 592
Low-cobalt diet for dyshidrotic eczema patients. 592
First-line therapies 592
Pompholyx: a review of clinical features, differential diagnosis, and management. 592
Acute and recurrent vesicular hand dermatitis. 593
Topical tacrolimus (FK 506) and mometasone furoate in treatment of dyshidrotic palmar eczema: a randomized, observer-blinded trial. 593
Efficacy and safety of pimecrolimus cream 1% in mild-to-moderate chronic hand dermatitis: a randomized, double-blind trial. 593
Second-line therapies 593
Oral alitretinoin in chronic refractory hand eczema: a “real life” case-series of 12 patients. 593
Successful retreatment with alitretinoin in patients with relapsed chronic hand eczema. 593
Efficacy and safety of oral alitretinoin (9-cis retinoic acid) in patients with severe chronic hand eczema refractory to topical corticosteroids: results of a randomized, double-blind, placebo-controlled, multicentre trial. 593
Local narrowband UVB phototherapy vs. local PUVA in the treatment of chronic hand eczema. 593
Comparison of localized high-dose UVA1 irradiation versus topical cream psoralen–UVA for treatment of chronic vesicular dyshidrotic eczema. 593
Oral vs. bath PUVA using 8-methoxypsoralen for chronic palmoplantar eczema. 593
Regression of relapsing dyshidrotic eczema after treatment of concomitant hyperhidrosis with botulinum toxin-A. 593
Pompholyx: what’s new? 593
Third-line therapies 593
Long-term follow-up of eczema patients treated with cyclosporine. 593
Low-dose oral methotrexate treatment for recalcitrant palmoplantar pompholyx. 593
Azathioprine in dermatological practice. An overview with special emphasis of its use in non-bullous inflammatory dermatoses. 593
Dyshidrotic eczema treated with mycophenolate mofetil. 594
Recalcitrant hand pompholyx: variable response to etanercept. 594
Long-term results of radiotherapy in patients with chronic palmo-plantar eczema or psoriasis. 594
191 Porokeratoses 595
Management strategy 595
Specific investigations 595
Dermoscopy for the diagnosis of porokeratosis. 595
First-line therapies 595
Porokeratosis of Mibelli: successful treatment with cryosurgery. 595
Cryosurgery of porokeratosis plantaris discreta. 595
Second-line therapies 595
Fluorouracil ointment treatment of porokeratosis of Mibelli. 595
Disseminated superficial porokeratosis: rapid therapeutic response to 5-fluorouracil. 596
Porokeratosis of Mibelli: successful treatment with 5% imiquimod cream. 596
Disseminated superficial actinic porokeratosis treated effectively with topical imiquimod 5% cream. 596
Disseminated superficial actinic porokeratosis: treatment with topical tacalcitol. 596
Disseminated superficial actinic porokeratosis responding to calcipotriol. 596
Third-line therapies 596
Generalized linear porokeratosis: a rare entity with excellent response to acitretin. 596
Disseminated porokeratosis Mibelli treated with Ro 10- 9359. 596
Treatment of disseminated superficial actinic porokeratosis with a new aromatic retinoid (Ro 10-9359). 596
Porokeratosis plantaris, palmaris, et disseminata. Report of a case and treatment with isotretinoin. 596
A case of extensive linear porokeratosis with evaluation of topical tretinoin versus 5-fluorouracil as treatment modalities. 596
Topical tretinoin in Indian male with zosteriform porokeratosis. 596
Treatment of porokeratosis of Mibelli with CO2 laser vaporization versus surgical excision with split-thickness skin graft. 596
Reticulate porokeratosis – successful treatment with CO2-laser vaporization. 596
Treatment of lichen amyloidosis (LA) and disseminated superficial porokeratosis (DSP) with frequency-doubled Q-switched Nd:YAG laser. 596
Successful treatment of porokeratosis with 585 nm pulsed dye laser irradiation. 596
Treatment of disseminated superficial actinic porokeratosis (DSAP) with the Q-switched ruby laser. 597
Fractional photothermolysis: a novel treatment for disseminated superficial actinic porokeratosis. 597
Successful treatment of disseminated superficial actinic porokeratosis with methyl aminolevulinate-photodynamic therapy. 597
Topical photodynamic therapy in disseminated superficial actinic porokeratosis. 597
Successful treatment of porokeratosis of Mibelli with diamond fraise dermabrasion. 597
Linear porokeratosis: successful treatment with diamond fraise dermabrasion. 597
The use of fluor-hydroxy pulse peel in actinic porokeratosis. 597
Dexamethasone pulse treatment in disseminated porokeratosis of Mibelli. 597
Diclofenac sodium 3% gel as a potential treatment for disseminated superficial actinic porokeratosis. 597
Treatment of disseminated superficial actinic porokeratosis with topical diclofenac gel: a case series. 597
Porokeratosis of Mibelli: successful treatment with 5 percent topical imiquimod and topical 5 percent 5- fluorouracil. 597
Photodynamic therapy combined with CO2 laser vaporization on disseminated superficial actinic porokeratosis: a report of 2 cases on the face. 597
192 Porphyria cutanea tarda 598
Management strategy 598
Specific investigations 598
Porphyria cutanea tarda: clinical features and laboratory findings in forty patients. 598
Hepatitis C, porphyria cutanea tarda and liver iron: an update. 598
Porphyria cutanea tarda, hepatitis C, and HFE gene mutations in North America. 598
Hepatocellular carcinoma risk in patients with porphyria cutanea tarda. 598
First-line therapies 599
The effect of phlebotomy therapy in porphyria cutanea tarda. 599
Childhood-onset familial porphyria cutanea tarda: effects of therapeutic phlebotomy. 599
Plasma ferritin levels as a guide to the treatment of porphyria cutanea tarda by venesection. 599
Treatment of porphyria cutanea tarda with chloroquine. 599
Childhood-onset porphyria cutanea tarda: successful therapy with low-dose hydroxychloroquine (Plaquenil). 599
Choice of therapy in porphyria cutanea tarda. 599
Hemochromatosis (HFE) gene mutations and response to chloroquine in porphyria cutanea tarda. 599
Second-line therapies 599
Liver iron overload and desferrioxamine treatment of porphyria cutanea tarda. 599
Haemodialysis-related porphyria cutanea tarda and treatment by recombinant human erythropoietin. 599
Successful treatment of haemodialysis-related porphyria cutanea tarda with deferoxamine. 600
Third-line therapies 600
Highly active antiretroviral therapy leading to resolution of porphyria cutanea tarda in a patient with AIDS and hepatitis C. 600
Dramatic resolution of skin lesions associated with porphyria cutanea tarda – interferon-alpha therapy in a case of chronic hepatitis C. 600
High-dose vitamin E lowers urine porphyrin levels in patients affected by porphyria cutanea tarda. 600
Porphyria cutanea tarda: a possible role for ascorbic acid. 600
Removal of plasma porphyrins with high-flux hemodialysis in porphyria cutanea tarda associated with end stage renal disease. 600
Treatment of hemodialysis related porphyria cutanea tarda with plasma exchange. 600
The adsorption of porphyrins and porphyria precursors by sorbents: a potential therapy for the porphyrias. 600
Metabolic alkalinization therapy in porphyria cutanea tarda. 600
Cimetidine in the treatment of porphyria cutanea tarda. 600
Management of porphyria cutanea tarda in the setting of chronic renal failure – case report and review. 600
Successful and safe treatment of hypertrichosis by high-intensity pulses of noncoherent light in a patient with hepatoerythropoietic porphyria. 600
193 Port wine stain (‘nevus flammeus’) 601
Management strategy 601
Specific investigations 602
Facial port wine stain and Sturge–Weber syndrome. 602
Sturge–Weber syndrome in patients with facial port- wine stain. 602
Facial port-wine stain: when to worry? 602
Location of port wine stains and the likelihood of ophthalmic and/or central nervous system complications. 602
Sturge–Weber syndrome and dermatomal facial port wine stains: incidence, association with glaucoma, and pulsed tunable dye laser treatment effectiveness. 602
Sturge–Weber syndrome. The current neuroradiologic data. 602
First-line therapies 602
Anatomic differences of port wine stains in response to treatment with pulsed dye laser. 602
Facial port wine stains in childhood: prediction of the rate of improvement as a function of the age of the patient, size and location of the port wine stain and the number of treatments with the pulsed dye (585 nm) laser. 602
Efficacy of early treatment of facial port wine stains in newborns: A review of 49 cases. 602
Treatment of port wine stains (capillary malformations) with the flash lamp pumped pulsed dye laser. 603
Double pass 595 nm pulsed dye laser at a 6 minute interval for the treatment of port-wine stains is not more effective than single pass. 603
High-fluence modified pulsed dye laser photocoagulation with dynamic cooling of port wine stains in infancy. 603
Redarkening of port-wine stains 10 years after pulsed-dye-laser treatment. 603
Pain relief measures and cooling devices 603
Effects of percutaneous local anaesthetics on pain reduction during pulse dye laser treatment of port wine stains. 603
The S-Caine peel: a novel topical anesthetic for cutaneous laser surgery. 603
Effect of the topical anesthetic EMLA on the efficacy of pulsed dye laser treatment of port wine stains. 603
Cryogen spray cooling and higher fluence pulsed dye laser treatment improve port wine stain clearance while minimizing epidermal damage. 603
General anesthesia for pediatric dermatologic procedures: risks and complications. 603
Second-line therapies 603
Split-face comparison of intense pulsed light with short- and long-pulsed dye lasers for the treatment of port-wine stains. 603
Intense pulsed light source for the treatment of dye laser resistant port-wine stains. 603
Treatment of hypertrophic and resistant port wine stains with a 755 nm laser: a case series of 20 patients. 604
Treatment endpoints for resistant port wine stains with a 755 nm laser. 604
Long-pulsed neodymium: yttrium–aluminum–garnet laser treatment for port wine stains. 604
Combined 595 nm and 1064 nm laser irradiation of recalcitrant and hypertrophic port-wine stains in children and adults. 604
A direct comparison of pulsed dye, alexandrite, KTP and Nd:YAG lasers and IPL in patients with previously treated capillary malformations. 604
Third-line therapies 604
Potassium titanyl phosphate laser treatment of resistant port-wine stains. 604
Pilot study examining the combined use of pulsed dye laser and topical imiquimod versus laser alone for treatment of port wine stain birthmarks. 604
Enhanced port-wine stain lightening achieved with combined treatment of selective photothermolysis and imiquimod. 605
Photodynamic therapy of port-wine stains: long-term efficacy and complication in Chinese patients. 605
Long-term blood vessel removal with combined laser and topical rapamycin antiangiogenic therapy: implications for effective port wine stain treatment. 605
194 Pregnancy dermatoses 606
Pruritic urticarial papules and plaques of pregnancy 606
Management strategy 606
Specific Investigations 606
A comparative study of toxic erythema of pregnancy and herpes gestationis. 606
A comparative histopathological study of polymorphic eruption of pregnancy and herpes gestationis. 606
An immunoelectron microscopy study of the relationship between herpes gestationis and polymorphic eruption of pregnancy. 606
Polymorphic eruption of pregnancy: clinicopathology and potential trigger factors in 181 patients. 606
First-line therapies 607
195 Pretibial myxedema 612
Management strategy 612
Specific investigations 612
Pretibial myxedema. 612
Pretibial myxedema as the initial manifestation of Graves’ disease. 612
Observing pretibial myxedema in patients with Graves’ disease using digital infrared thermal imaging and high-resolution ultrasonography: for better records, early detection and further investigation. 612
First-line therapies 613
Dermopathy of Graves disease (pretibial myxedema): review of 150 cases. 613
Treatment of pretibial myxedema with topical steroid ointment application with sealing cover in Graves’ patients. 613
Intralesional triamcinolone therapy for pretibial myxedema. 613
Pretibial myxedema: a review of the literature and case report. 613
Pretibial myxoedema with autoimmunity and hyperplasia treated with glucocorticoids and surgery. 613
Second-line therapies 613
Pentoxifylline inhibits the proliferation and glycosaminoglycan synthesis of cultured fibroblasts derived from patients with Graves’ ophthalmopathy and pretibial myxedema. 613
Successful combined pentoxifylline and intralesional triamcinolone acetonide treatment of severe pretibial myxedema. 613
Third-line therapies 613
Pretibial myxedema and high-dose intravenous immunoglobulin treatment. 613
Lack of response of elephantiasic pretibial myxoedema to treatment with high-dose intravenous immunoglobulins. 613
Corticoid therapy for pretibial myxedema: observations on the long-acting thyroid stimulator. 613
Refractory pretibial myxoedema with response to intralesional insulin-like growth factor 1 antagonist (octreotide): downregulation of hyaluronic acid production by the lesional fibroblasts. 614
Octreotide and Graves’ ophthalmopathy and pretibial myxoedema. 614
Lack of effect of long-term octreotide therapy in severe thyroid-associated dermopathy. 614
Effect of plasmapheresis and steroid treatment on thyrotropin binding inhibitory immunoglobulins in a patient with exophthalmos and a patient with pretibial myxedema. 614
Beneficial effects of plasmapheresis followed by immunosuppressive therapy in pretibial myxedema. 614
Pretibial myxedema (elephantiasic form): treatment with cytotoxic therapy. 614
Successful combined surgical and octreotide treatment of severe pretibial myxoedema reviewed after 9 years. 614
Pretibial myxedema. 614
Treatment-resistant elephantiasic thyroid dermopathy responding to rituximab and plasmapheresis. 614
Elephantiasic pretibial myxedema: a novel treatment for an uncommon disorder. 614
196 Prurigo nodularis 615
Management strategy 615
Specific investigations 615
First-line therapies 616
Prurigo nodularis. 616
Nodular prurigo: a clinicopathological study of 46 patients. 616
Treatment of nodular prurigo with cyclosporine (treat the disease, not just the symptoms). 616
Use of occlusive membrane in prurigo nodularis. 616
An occlusive dressing containing betamethasone valerate 0.1% for the treatment of prurigo nodularis. 616
Second-line therapies 616
Treatment of prurigo nodularis with topical capsaicin. 616
Treatment of prurigo nodularis: use of cryosurgery and intralesional steroids plus lidocaine. 616
Cryotherapy improves prurigo nodularis. 616
UV treatment of generalised prurigo nodularis. 616
Narrow-band ultraviolet B phototherapy in patients with recalcitrant nodular prurigo. 616
Local photochemotherapy in nodular prurigo. 616
Longterm results of topical trioxalen PUVA in lichen planus and nodular prurigo. 616
Phototherapy in nodular prurigo. 617
Monochromatic excimer light (308 nm) in the treatment of prurigo nodularis. 617
UVB 308-nm excimer light and bath PUVA: combination therapy is very effective in the treatment of prurigo nodularis. 617
Third-line therapies 617
Nodular prurigo responding to topical tacrolimus. 617
Double-blind, right/left comparison of calcipotriol ointment and betamethasone ointment in the treatment of prurigo nodularis. 617
Topical vitamin D3 (tacalcitol) for steroid-resistant prurigo. 617
Successful immunotherapy of chronic nodular prurigo with topical dinitrochlorobenzene. 617
Nodular prurigo successfully treated with the pulsed dye laser. 617
Thalidomide treatment of prurigo nodularis. 617
Sequential combined therapy with thalidomide and narrowband (TL01) UVB in the treatment of prurigo nodularis. 617
Thalidomide treatment for prurigo nodularis in human immunodeficiency virus-infected subjects: efficacy and risk of neuropathy. 617
Thalidomide in 42 patients with prurigo nodularis Hyde. 617
Efficacy of thalidomide in the treatment of prurigo nodularis. 617
Treatment of refractory prurigo nodularis with lenalidomide. 617
Nodular prurigo responds to cyclosporine. 618
Antipruritic effect of cyclosporine microemulsion in prurigo nodularis: results of a case series. 618
Atopic prurigo nodularis responds to intravenous immunoglobulins. 618
Therapeutic hotline. Treatment of prurigo nodularis and lichen simplex chronicus with gabapentin. 618
Nodular prurigo responsive to azathiaprine. 618
Uncontrollable prurigo nodularis effectively treated by roxithromycin and tranilast. 618
Prurigo nodularis (Hyde) treated with Tigason. 618
Etretinate and nodular prurigo. 618
Persistent prurigo nodularis responsive to initiation of combination therapy with raltegravir. 618
Hypnosis and acupuncture (hypnopuncture) for prurigo nodularis: a case report. 618
197 Prurigo pigmentosa 619
Management strategy 619
Specific investigations 619
Prurigo pigmentosa on a patient with soft-drink ketosis. 619
198 Pruritus 621
Management strategy 621
Specific investigations 621
Itch and pruritus: what are they and how should itches be classified? 621
Clinical classification of itch: a position paper of the International Forum for the Study of Itch. 621
Neurophysiological and neurochemical basis of modern pruritus treatment. 621
Pruritus of undetermined origin. 622
Ultraviolet phototherapy for pruritus. 622
Pruritus in chronic liver disease: mechanisms and treatment. 622
Neuropathic itch 622
Brachioradial pruritus as a result of cervical spine pathology: the results of a magnetic resonance tomography study. 622
Brachioradial pruritus: a trigger for generalization of itch. 622
First-line therapies 622
Successful treatment of notalgia paresthetica with topical capsaicin: vehicle-controlled, double-blind, crossover study. 622
Solar (brachioradial) pruritus – response to capsaicin cream. 622
Second-line therapies 622
Gabapentin treatment for notalgia paresthetica, a common isolated peripheral sensory neuropathy. 622
Brachioradial pruritus: response to treatment with gabapentin. 622
Brachioradial pruritus: report of a new case responding to gabapentin. 622
Gabapentin treatment for brachioradial pruritus. 622
Pregabalin in the treatment of chronic pruritus. 622
Cholestatic itch 622
The itch of liver disease. 623
Update on the treatment of the pruritus of cholestasis. 623
First-line therapies 623
Rifampin is safe for treatment of pruritus due to chronic cholestasis: a meta-analysis of prospective randomized-controlled trials. 623
The efficacy and safety of bile acid binding agents, opioid antagonists, or rifampin in the treatment of cholestasis-associated pruritus. 623
Efficacy and safety of oral naltrexone treatment for pruritus of cholestasis, a crossover, double blind, placebo-controlled study. 623
Oral nalmefene therapy reduces scratching activity due to the pruritus of cholestasis: a controlled study. 623
Effects of naloxone infusions in patients with the pruritus of cholestasis. A double-blind, randomized, controlled trial. 623
Second-line therapies 623
Double-blind placebo-controlled clinical trial of microporous cholestyramine in the treatment of intra- and extra-hepatic cholestasis: relationship between itching and serum bile acids. 623
Randomised controlled trials of ursodeoxycholic-acid therapy for primary biliary cirrhosis: a meta-analysis. 623
The potent bile acid sequestrant colesevelam is not effective in cholestatic pruritus: results of a double-blind, randomized, placebo-controlled trial. 623
Sertraline as a first-line treatment for cholestatic pruritus. 623
Long-term efficacy of sertraline as a treatment for cholestatic pruritus in patients with primary biliary cirrhosis. 623
Third-line therapies 624
Treatment of severe refractory pruritus with fractionated plasma separation and adsorption (Prometheus). 624
Therapy of intractable pruritus with MARS. 624
Extracorporeal albumin dialysis: a procedure for prolonged relief of intractable pruritus in patients with primary biliary cirrhosis. 624
Treatment of intractable pruritus in drug induced cholestasis with albumin dialysis: a report of two cases. 624
Phototherapy for primary biliary cirrhosis. 624
Efficacy of lidocaine in the treatment of pruritus in patients with chronic cholestatic liver diseases. 624
Preliminary observation with dronabinol in patients with intractable pruritus secondary to cholestatic liver disease. 624
Itch associated with cholestasis of pregnancy 624
First-line therapies 624
Intrahepatic cholestasis of pregnancy: amelioration of pruritus by UDCA is associated with decreased progesterone disulphates in urine. 624
Intrahepatic cholestasis of pregnancy: a randomized controlled trial comparing dexamethasone and ursodeoxycholic acid. 624
Second-line therapies 624
Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy. 624
A randomised controlled trial of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of gestational cholestasis. 624
Efficacy and safety of ursodeoxycholic acid versus cholestyramine in intrahepatic cholestasis of pregnancy. 625
Renal itch 625
First-line therapies 625
Narrowband ultraviolet B phototherapy for patients with refractory uraemic pruritus: a randomized controlled trial. 625
Treatment of uremic pruritus with narrowband ultraviolet B phototherapy: an open pilot study. 625
Generalized pruritus treated with narrowband UVB. 625
Ultraviolet phototherapy of uremic pruritus. Long-term results and possible mechanism of action. 625
Gabapentin: a promising drug for the treatment of uremic pruritus. 625
Gabapentin therapy for pruritus in haemodialysis patients: a randomized, placebo-controlled, double-blind trial. 625
Use of pregabalin in the management of chronic uremic pruritus. 625
Pregabalin versus gabapentin in the treatment of neuropathic pruritus in maintenance hemodialysis patients: a prospective crossover study. 626
Randomised crossover trial of naltrexone in uraemic pruritus. 626
Naltrexone does not relieve uremic pruritus: results of a randomized placebo-controlled crossover study. 626
Kappa-opioid system in uremic pruritus: multicenter, randomized, double-blind, placebo-controlled clinical studies. 626
Nalfurafine hydrochloride for the treatment of pruritus. 626
Effect of skin care with an emollient containing a high water content on mild uremic pruritus. 626
Second-line therapies 626
Zinc sulfate for relief of pruritus in patients on maintenance hemodialysis. 626
Topical capsaicin therapy for uremic pruritus in patients on hemodialysis. 626
Acupuncture in haemodialysis patients at the Quchi (LI11) acupoint for refractory uraemic pruritus. 626
Effects of homeopathic treatment on pruritus of haemodialysis patients: a randomised placebo-controlled double-blind trial. 626
Third-line therapies 626
Cholestyramine in uraemic pruritus. 626
Relief of idiopathic generalized pruritus in dialysis patients treated with activated oral charcoal. 626
Thalidomide for the treatment of uremic pruritus: a crossover randomized double-blind trial. 626
A study on pruritus after parathyroidectomy for secondary hyperparathyroidism. 627
Itch associated with malignancy 627
199 Pruritus ani 629
Management strategy 629
Specific investigations 629
Allergic contact dermatitis in patients with anogenital complaints. 629
Pruritus ani as a manifestation of systemic contact dermatitis: resolution with dietary nickel restriction. 629
Treatment of persistent pruritus ani in a combined colorectal and dermatological clinic. 629
Abnormal transient internal sphincter relaxation in idiopathic pruritus ani: physiological evidence from ambulatory monitoring. 629
Pruritus ani. Causes and concerns. 630
First-line therapies 630
1% hydrocortisone ointment is an effective treatment of pruritus ani: a pilot randomized control crossover trial. 630
Randomized study of topical tacrolimus ointment as possible treatment for resistant idiopathic pruritus ani. 630
Idiopathic perianal pruritus: washing compared with topical corticosteroids. 630
Second-line therapies 630
Topical capsaicin: a novel and effective treatment for idiopathic intractable pruritus ani: a randomised, placebo controlled, crossover study. 630
A liquid-forming acrylate cream for the treatment of anal pruritus. 630
Third-line therapies 630
The use of intralesional triamcinolone hexacetonide in the treatment of idiopathic pruritus ani. 630
Intradermal injection of methylene blue for the treatment of refractory pruritus ani. 630
A new concept of the anatomy of the anal sphincter mechanism and the physiology of defecation. XXIII. An injection technique for the treatment of idiopathic pruritus ani. 630
200 Pruritus vulvae 631
Management strategy 631
Specific investigations 631
An approach to the treatment of anogenital pruritus. 631
Recurrent vulvovaginal candidosis: focus on the vulva. 632
Pruritus in diabetes mellitus: investigation of prevalence and correlation with diabetes. 632
Vulvar intraepithelial neoplasia (VIN) diagnostic and therapeutic challenges. 632
Prospective study of patch testing in patients with vulval pruritus. 632
Patients with vulval pruritus: patch test results. 632
First-line therapies 632
Pimecrolimus 1% cream for pruritus in postmenopausal diabetic women with vulvar lichen simplex chronicus: a prospective non-controlled case series. 632
Efficacy of topical pimecrolimus in the treatment of chronic vulvar pruritus. A prospective case series: A non-controlled, open-label study. 632
Contact dermatitis of the vulva. 632
Lichen simplex chronicus (atopic/neurodermatitis) of the anogenital region. 632
Pruritus vulvae in prepubertal children. 632
The common problem of vulvar pruritus. 632
Vulvovaginal dryness and itching. 632
Second-line therapies 632
Efficacy of topical oxatomide in women with pruritus vulva. 632
Subcutaneous injection of triamcinolone acetonide in the treatment of chronic vulvar pruritus. 632
Third-line therapies 633
Effectiveness of treating non-specific pruritus vulvae with topical steroids: a randomized controlled trial. 633
56 cases of chronic pruritus vulvae treated with acupuncture. 633
Chronic vulvovaginal pruritus treated successfully with GnRH analogue. 633
Hypnosis in a case of long-standing idiopathic itch. 633
201 Pseudofolliculitis barbae 634
Management strategy 634
Specific investigations 634
Scar sarcoidosis in pseudofolliculitis barbae. 634
Pseudofolliculitis barbae induced by oral minoxidil. 634
Disseminated cryptococcosis presenting as pseudofolliculitis in an AIDS patient. 635
Hyperplastic pseudofolliculitis barbae associated with cyclosporine. 635
Hypertrophic pseudofolliculitis in white renal transplant recipients. 635
An unusual Ala12Thr polymorphism in the 1A alpha- helical segment of the companion layer-specific keratin K6hf: evidence for a risk factor in the etiology of the common hair disorder pseudofolliculitis barbae. 635
Epiluminescence dermatoscopy enhanced patient compliance and achieved treatment success in pseudofolliculitis barbae. 635
First-line therapies 635
Pseudofolliculitis of the beard. 635
Pseudofolliculitis barbae. Medical consequences of interracial friction in the US Army. 635
Pseudofolliculitis barbae. 2. Treatment. 635
Pseudofolliculitis barbae and related disorders. 635
Pseudofolliculitis barbae and acne keloidalis nuchae. 635
Second-line therapies 635
Pseudofolliculitis of the beard and topically applied tretinoin. 635
Pseudofolliculitis: revised concepts of diagnosis and treatment. Report of three cases in women. 635
Twice-daily applications of benzoyl peroxide 5%/clindamycin 1% gel versus vehicle in the treatment of pseudofolliculitis barbae. 636
Treatment of pseudofolliculitis barbae with topical glycolic acid: a report of two studies. 636
Third-line therapies 636
Comparative evaluation of long pulse alexandrite laser and intense pulsed light systems for pseudofolliculitis barbae treatment with one year of followup. 636
Low-fluence 1064-nm laser hair reduction for pseudofolliculitis barbae in skin types IV, V, and VI. 636
Topical eflornithine hydrochloride improves the effectiveness of standard laser hair removal for treating pseudofolliculitis barbae: a randomized, double-blinded, placebo- controlled trial. 636
Pseudofolliculitis barbae. 636
Modified superlong pulse 810 nm diode laser in the treatment of pseudofolliculitis barbae in skin types V and VI. 636
Pseudofolliculitis of the neck and the shoulder: a new effective treatment with alexandrite laser. 636
Treatment of pseudofolliculitis with a pulsed infrared laser. 637
Laser-assisted hair removal for darker skin types. 637
Treatment of pseudofolliculitis barbae in skin types IV, V, and VI with a long-pulsed neodymium:yttrium aluminum garnet laser. 637
Treatment of pseudofolliculitis barbae using the long-pulse Nd:YAG laser on skin types V and VI. 637
Surgical depilation for the treatment of pseudofolliculitis or local hirsutism of the face: experience in the first 40 patients. 637
202 Pseudoxanthoma elasticum 638
Management strategy 638
Specific investigations 638
Pseudoxanthoma elasticum. 638
First-line therapies 638
Pseudoxanthoma elasticum: a connective tissue disease or a metabolic disorder at the genome/environment interface? 638
Pseudoxanthoma elasticum is a metabolic disease. 638
Long-term effectiveness of intravitreal bevacizumab for choroidal neovascularization secondary to angioid streaks in pseudoxanthoma elasticum. 638
Second-line therapies 639
Pseudoxanthoma elasticum and mitral valve prolapse. 639
Third-line therapies 639
Other therapies 639
A randomized controlled trial of oral phosphate binders in the treatment of pseudoxanthoma elasticum. 639
Pseudoxanthoma elasticum, the paradigm of heritable ectopic mineralization disorders: can diet help? 639
203 Psoriasis 640
Management strategy 640
Guttate psoriasis 641
Inverse psoriasis 641
Impetigo herpetiformis 641
Specific investigations 642
From the Medical Board of the National Psoriasis Foundation: monitoring and vaccinations in patients treated with biologics for psoriasis. 642
Cyclosporine and psoriasis: 2008 National Psoriasis Foundation Consensus Conference. 642
Methotrexate and psoriasis: 2009. National Psoriasis Foundation Consensus Conference. 642
Methotrexate in psoriasis: consensus conference. 642
First-line therapies 642
A randomized, double-blind, vehicle-controlled study of a novel liposomal dithranol formulation in psoriasis. 642
Efficacy of topical 5% liquor carbonis detergens vs. its emollient base in the treatment of psoriasis. 643
The role of salicylic acid in the treatment of psoriasis. 643
Evaluation of the efficacy and safety of clobetasol propionate spray in the treatment of plaque-type psoriasis. 643
The efficacy and tolerability of clobetasol propionate foam 0.05% in the treatment of mild to moderate plaque-type psoriasis of nonscalp regions. 643
Clobetasol propionate shampoo 0.05%: a new option to treat patients with moderate to severe scalp psoriasis. 643
An investigator-masked comparison of the efficacy and safety of twice daily applications of calcitriol 3 µg/g ointment vs. calcipotriol 50 µg/g ointment in subjects with mild to moderate chronic plaque-type psoriasis. 643
Once daily treatment of psoriasis with tacalcitol compared with twice daily treatment with calcipotriol. A double-blind trial. 643
A 52-week randomized safety study of a calcipotriol/betamethasone dipropionate two-compound product (Dovobet/Daivobet/Taclonex) in the treatment of psoriasis vulgaris. 643
Tazarotene cream in the treatment of psoriasis: two multicenter, double-blind, randomized, vehicle-controlled studies of the safety and efficacy of tazarotene creams 0.05% and 0.1% applied once daily for 12 weeks. 643
Tacrolimus ointment is effective for facial and intertriginous psoriasis. 643
Pimecrolimus cream 1% in the treatment of intertriginous psoriasis: a double-blind, randomized study. 644
The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead Sea. 644
Second-line therapies 644
Components of the Goeckerman regimen. 644
Narrowband UV-B produces superior clinical and histopathological resolution of moderate-to-severe psoriasis in patients compared with broadband UV-B. 644
Randomized double-blind trial of the treatment of chronic plaque psoriasis: efficacy of psoralen-UV-A therapy vs. narrowband UV-B therapy. 644
PUVA therapy for psoriasis: comparison of oral and bath-water delivery of 8-methoxypsoralen. 644
Efficacy and safety results from the randomized controlled comparative study of adalimumab vs. methotrexate vs. placebo in patients with psoriasis (CHAMPION). 644
A double-blind, placebo-controlled trial of acitretin for the treatment of psoriasis. 644
Acitretin plus UVB therapy for psoriasis. Comparisons with placebo plus UVB and acitretin alone. 645
Photochemotherapy for severe psoriasis without or in combination with acitretin: a randomized, double-blind comparison study. 645
Methotrexate versus cyclosporine in moderate-to-severe chronic plaque psoriasis. 645
Etanercept treatment for children and adolescents with plaque psoriasis. 645
Adalimumab therapy for moderate to severe psoriasis: a randomized, controlled phase III trial. 645
A randomized comparison of continuous vs. intermittent infliximab maintenance regimens over 1 year in the treatment of moderate-to-severe plaque psoriasis. 645
Efficacy and safety of ustekinumab, a human interleukin- 12/23 monoclonal antibody, in patients with psoriasis: 52-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 2). 645
Third-line therapies 645
Combination treatments for psoriasis: a systematic review and meta-analysis. 646
Clinical efficacy of a 308 nm excimer laser for treatment of psoriasis vulgaris. 646
Targeted UVB phototherapy for psoriasis: a preliminary study. 646
Efficacy of the pulsed dye laser in the treatment of localized recalcitrant plaque psoriasis: a comparative study. 646
Weekly pulse dosing schedule of fluorouracil: a new topical therapy for psoriasis. 646
Weekly psoriasis therapy using intralesional fluorouracil. 646
Clinical assessment of patients with recalcitrant psoriasis in a randomized, observer-blind, vehicle-controlled trial using indigo naturalis. 646
Sulfasalazine improves psoriasis. A double-blind analysis. 646
Mycophenolate mofetil (CellCept) for psoriasis: a two- center, prospective, open-label clinical trial. 646
Hydroxyurea in the management of therapy resistant psoriasis. 646
6-Thioguanine treatment of psoriasis: experience in 81 patients. 647
Pulse dosing of thioguanine in recalcitrant psoriasis. 647
Azathioprine in psoriasis. 647
Systemic tacrolimus (FK 506) is effective for the treatment of psoriasis in a double-blind, placebo-controlled study. 647
Treatment of psoriasis with fumaric acid esters: results of a prospective multicentre study: German Multicentre Study. 647
Use of rifampin with penicillin and erythromycin in the treatment of psoriasis. Preliminary report. 647
Therapeutic trials with oral colchicine in psoriasis. 647
Propylthiouracil in psoriasis: results of an open trial. 647
Cryotherapy for psoriasis. 647
Psoriasis of the scalp treated with Grenz rays or topical corticosteroid combined with Grenz rays. A comparative randomized trial. 647
Efficacy and safety of leflunomide in the treatment of psoriatic arthritis and psoriasis: a multinational, double-blind, randomized, placebo-controlled clinical trial. 647
Golimumab, a human TNF-alpha antibody, administered every 4 weeks as a subcutaneous injection in psoriatic arthritis. Clinical efficacy, radiographic, and safety findings through 1 year of the randomized, placebo-controlled, GO-REVEAL® study. 647
Successful treatment of moderate to severe plaque psoriasis with the PEGylated Fab’ certolizumab pegol. Results of a phase II randomised, placebo-controlled trial with a re-treatment extension. 648
Anti-interleukin-17 monoclonal antibody ixekizumab in chronic plaque psoriasis. 648
Erythrodermic psoriasis 648
First-line therapies 648
Use of short-course class 1 topical glucocorticoid under occlusion for the rapid control of erythrodermic psoriasis. 648
Second-line therapies 648
Management of erythrodermic psoriasis with low-dose cyclosporine. 648
Life-threatening pustular and erythrodermic psoriasis responding to infliximab. 648
Treatment of erythrodermic psoriasis with etanercept. 648
Treatment of pustulous and erythrodermic psoriasis with PUVA therapy and methotrexate. 648
Third-line therapies 649
The treatment of psoriasis with etretinate and acitretin: a follow up of actual use. 649
Accidental success with carbamazepine for psoriatic erythroderma. 649
Pustular psoriasis 649
First-line therapies 649
Systemic corticosteroids and folic acid antagonists in the treatment of generalized pustular psoriasis. Evaluation and prognosis based on the study of 104 cases. 649
Isotretinoin vs etretinate therapy in generalized pustular and chronic psoriasis. 649
Generalized pustular psoriasis (von Zumbusch) responding to cyclosporin A. 649
Infliximab in recalcitrant generalized pustular arthropatic psoriasis. 649
Pustular psoriasis induced by infliximab. 649
Long-term efficacy of adalimumab in generalized pustular psoriasis. 649
Second-line therapies 649
Etanercept at different dosages in the treatment of generalized pustular psoriasis: a case series. 650
Generalised pustular psoriasis: response to topical calcipotriol. 650
Third-line therapies 650
Colchicine in generalized pustular psoriasis: clinical response and antibody-dependent cytotoxicity by monocytes and neutrophils. 650
204 Psychogenic excoriation 651
Management strategy 651
Specific investigations 651
Psychogenic excoriation. Clinical features, proposed diagnostic criteria, epidemiology and approaches to treatment. 651
Characteristics of 34 adults with psychogenic excoriation. 652
Neurotic excoriations and dermatitis artefacta. 652
The psychiatric profile of patients with psychogenic excoriations. 652
Dermatology and conditions related to obsessive– compulsive disorder. 652
Neurotic excortiations: a diagnosis of exclusion. 652
First-line therapies 652
Psychopharmacology for dermatologic patients. 652
Improvement of chronic neurotic excoriations with oral doxepin therapy. 652
Second-line therapies 652
Sertraline in the treatment of neurotic excoriations and related disorders. 652
Paroxetine in a case of psychogenic pruritus and neurotic excoriations. 652
Third-line therapies 652
A double-blind trial of fluoxetine in pathologic skin picking. 652
An open clinical trial of fluvoxamine treatment of psychogenic excoriation. 652
Use of escitalopram in psychogenic excoriation. 652
Neurotic excoriations: a review and some new perspectives. 652
Neurotic excoriations: a personality evaluation. 653
Neurotic excoriations. 653
Clinical experience with pimozide: emphasis on its use in post-herpetic neuralgia. 653
Efficacy of olanzapine in the treatment of psychogenic excoriation. 653
The treatment of psychogenic excoriation and obsessive compulsive disorder using aripiprazole and fluoxetine. 653
Aripiprazole augmentation of venlafaxine in the treatment of psychogenic excoriation. 653
Naltrexone for neurotic excoriations. 653
Psychotherapeutic strategy and neurotic excoriations. 653
Treatment of facial scarring and ulceration resulting from acne excoriée with 585-nm pulsed dye laser irradiation and cognitive psychotherapy. 653
Acne excoriée: a case report of treatment using habit reversal. 653
The behavioral treatment of neurodermatitis through habit reversal. 653
Treatment of neurodermatitis by behavior therapy: a case study. 653
Using hypnosis to facilitate resolution of psychogenic excoriations in acne excoriée. 653
Narrow-band ultraviolet B as a potential alternative treatment for resistant psychogenic excoriation: an open-label study. 653
205 Pyoderma gangrenosum 654
Management strategy 654
Specific investigations 654
First-line therapies 654
Topical tacrolimus for pyoderma gangrenosum. 654
Topical tacrolimus in the management of peristomal pyoderma gangrenosum. 654
Pyoderma gangrenosum of the scalp. 654
Beclometasone inhaler used to treat pyoderma gangrenosum. 654
Sulfapyridine and sulphone-type drugs in dermatology. 655
Triamcinolone and pyoderma gangrenosum. 655
The successful use of minocycline in pyoderma gangrenosum – a report of seven cases and review of the literature. 655
Successful treatment of pyoderma gangrenosum with topical 0.5% nicotine cream. 655
Successful treatment of severe pyoderma gangrenosum with pimecrolimus cream 1%. 655
Pyoderma gangrenosum. A study of nineteen cases. 655
The treatment of pyoderma gangrenosum with sodium cromoglycate. 655
Second-line therapies 655
Treatment of pyoderma gangrenosum with cyclosporine: results in seven patients. 655
Pyoderma gangrenosum. Clinical and laboratory findings in 15 patients with special reference to polyarthritis. 655
Therapeutic efficacy in the treatment of pyoderma gangrenosum. 655
Third-line therapies 655
Infliximab for the treatment of pyoderma gangrenosum: a randomised, double blind, placebo controlled trial. 656
Improvement of pyoderma gangrenosum and psoriasis associated with Crohn’s disease with anti-tumor necrosis factor alpha monoclonal antibody. 656
Treatment of pyoderma gangrenosum with etanercept. 656
Adalimumab therapy for recalcitrant pyoderma gangrenosum. 656
Adalimumab for treatment of pyoderma gangrenosum. 656
An open-label pilot study of alefacept for the treatment of pyoderma gangrenosum. 656
Pyoderma gangrenosum. Response to cyclophosphamide therapy. 656
Intravenous cyclophosphamide pulses in the treatment of pyoderma gangrenosum associated with rheumatoid arthritis. Report of 2 cases and review of the literature. 656
Chlorambucil is an effective corticosteroid-sparing agent for recalcitrant pyoderma gangrenosum. 656
Pyoderma gangrenosum–response to topical nitrogen mustard. 656
Leukocytapheresis treatment for pyoderma gangrenosum. 656
Efficacy of granulocyte and monocyte adsorption apheresis for three cases of refractory pyoderma gangrenosum. 656
Granulocyte and monocyte adsorption apheresis for pyoderma gangrenosum. 656
Efficacy of human intravenous immune globulin in pyoderma gangrenosum. 656
Intravenous immunoglobulin for pyoderma gangrenosum. 657
Intravenous immunoglobulin is effective as a sole immunomodulatory agent in pyoderma gangrenosum unresponsive to systemic corticosteroids. 657
Clearing of pyoderma gangrenosum by intralesional cyclosporin A. 657
Resolution of severe pyoderma gangrenosum in a patient with streaking leukocyte factor disease after treatment with tacrolimus (FK506). 657
Recalcitrant pyoderma gangrenosum treated with systemic tacrolimus. 657
Successful therapy of refractory pyoderma gangrenosum and periorbital phlegmona with tacrolimus (FK506) in ulcerative colitis. 657
Crohn’s disease with cutaneous involvement. 657
Treatment of pyoderma gangrenosum with colchicine. 657
Case report. Severe pyoderma associated with familial Mediterranean fever: favorable response to colchicine in three patients. 657
Pyoderma gangrenosum with severe pharyngeal involvement. 657
Pyoderma gangrenosum chez un enfant: traitement par la thalidomide. 657
Pyoderma gangrenosum associated with Behçet’s syndrome – response to thalidomide. 657
Successful treatment of pyoderma gangrenosum with potassium iodide. 657
Mycophenolate mofetil and cyclosporine treatment for recalcitrant pyoderma gangrenosum. 657
Mycophenolate mofetil in pyoderma gangrenosum. 657
Pyoderma gangrenosum in myelodysplasia responding to granulocyte macrophage-colony stimulating factor (GM-CSF). 657
Pyoderma gangrenosum successfully treated with perilesional granulocyte-macrophage colony stimulating factor. 657
Treatment of pyoderma gangrenosum with methotrexate. 657
Topical platelet-derived growth factor accelerates healing of myelodysplastic syndrome-associated pyoderma gangrenosum. 658
Recombinant human epidermal growth factor enhances wound healing of pyoderma gangrenosum in a patient with ulcerative colitis. 658
Clofazimine. A new agent for treatment of pyoderma gangrenosum. 658
Pyoderma gangrenosum treated with hyperbaric oxygen therapy. 658
Superficial pyoderma gangrenosum responding to treatment with isotretinoin. 658
Targeted treatment of pyoderma gangrenosum in PAPA (pyogenic arthritis, pyoderma gangrenosum and acne) syndrome with the recombinant human interleukin-1 receptor antagonist anakinra. 658
Interleukin 23 expression in pyoderma gangrenosum and targeted therapy with ustekinumab. 658
Penile pyoderma gangrenosum successfully treated with topical imiquimod. 658
Monoclonal gammopathy of undetermined significance related pyoderma gangrenosum successfully treated with autologous peripheral blood stem cell transplantation. 658
Pyoderma gangrenosum treated successfully with visilizumab in patients with ulcerative colitis. 658
Two percent topical phenytoin sodium solution in treating pyoderma gangrenosum: a cohort study. 658
Split skin grafts in the treatment of pyoderma gangrenosum: a report of four cases. 658
Free flap coverage of pyoderma gangrenosum leg ulcers. 658
206 Pyogenic granuloma 659
Management strategy 659
Specific investigations 659
First-line therapies 659
Pyogenic granuloma in children. 659
Comparison of cyrotherapy and curettage for the treatment of pyogenic granuloma: a randomized trial. 659
Treatment of pyogenic granuloma by shave excision and laser photocoagulation. 660
The efficacy of silver nitrate cauterization for pyogenic granuloma of the hand. 660
Pyogenic granuloma – the quest for optimum treatment. Audit of treatment of 408 cases. 660
Cryotherapy in the treatment of pyogenic granuloma. 660
Second-line therapies 660
Treatment of pyogenic granuloma in children with the flashlamp-pumped pulsed dye laser. 660
The combined continuous-wave/pulsed carbon dioxide laser for treatment of pyogenic granuloma. 660
Pyogenic granulomas: treatment with the 1064-nm long-pulsed neodymium-doped yttrium aluminum garnet laser in 20 patients. 660
Third-line therapies 660
Surgical pearl: ligation of the base of a pyogenic granuloma-an atraumatic, simple, and cost-effective procedure. 660
Pyogenic granuloma in ten children treated with topical imiquimod. 661
Treatment of pyogenic granuloma by sodium tetradecyl sulfate sclerotherapy. 661
Photodynamic therapy with 5-aminolevulinic acid intralesionsal injection for pyogenic granuloma. 661
Pyogenic granuloma that responded to local injection of steroid. 661
Complete resolution of recurrent giant pyogenic granuloma on the palm of the hand following single dose of intralesional bleomycin injection. 661
Topical phenol as a conservative treatment for periungal pyogenic granuloma. 661
207 Radiation dermatitis 662
Management strategy 662
Specific investigations 662
Radio-induced malignancies of the scalp about 98 patients with 150 lesions and literature review. 662
First-line therapies 662
Evidence-based skin care management in radiation therapy: clinical update. 662
The prevention and management of acute skin reactions related to radiation therapy: a systematic review and practice guideline. 662
Topical corticosteroid therapy for acute radiation dermatitis: a prospective, randomized, double-blind study. 662
Phase III randomized trial of Calendula officinalis compared with trolamine for the prevention of acute dermatitis during irradiation for breast cancer. 663
Trolamine-containing topical emulsion: clinical applications in dermatology. 663
Skin treatment with Bepanthen cream versus no cream during radiotherapy – a randomized control trial. 663
Topical silver sulfadiazine for the prevention of acute dermatitis during irradiation for breast cancer. 663
Second-line therapies 663
Phase 2 study of silver leaf dressing for treatment of ration-induced dermatitis in patients receiving radiotherapy to the head and neck. 663
Silver leaf nylon dressing to prevent radiation dermatitis in patients undergoing chemotherapy and external beam radiotherapy to the perineum. 663
Assessing the effectiveness of Dead Sea products as prophylactic agents for acute radiochemotherapy-induced skin and mucosal toxicity in patients with head and neck cancers: a phase 2 study. 663
The cytoprotective effect of amifostine in acute radiation dermatitis: a retrospective analysis. 663
Prophylactic effect of pentoxifylline on radiotherapy complications: a clinical study. 663
Celecoxib reduces skin damage after radiation: selective reduction of chemokine and receptor mRNA expression in irradiated skin but not irradiated mammary tumor. 663
Topical amitriptyline, ketamine, and lidocaine in neuropathic pain caused by radiation skin reaction: a pilot study. 663
Third-line therapies 663
Chronic radiodermatitis injury after cardiac catheterization. 664
208 Raynaud disease and phenomenon 665
Management strategy 665
Specific investigations 665
Nailfold digital capillaroscopy in 447 patients with connective tissue disease and Raynaud’s disease. 665
Assessment of nailfold capillaroscopy by × 30 digital epiluminescence (dermoscopy) in patients with Raynaud phenomenon. 665
First-line therapies 665
Controlled double-blind trial of the clinical effect of nifedipine in the treatment of idiopathic Raynaud’s phenomenon. 666
Comparison of intravenous infusions of iloprost and oral nifedipine in treatment of Raynaud’s phenomenon in patients with systemic sclerosis: a double blind randomised study. 666
To compare the efficacy and safety of nifedipine sustained release with Ginkgo biloba extract to treat patients with primary Raynaud’s phenomenon in South Korea: Korean Raynaud study (KOARA study). 666
A double-blind placebo controlled crossover randomized trail of diltiazem in Raynaud’s phenomenon. 666
Digital vascular response to topical glyceryl trinitrate, as measured by laser Doppler imaging, in primary Raynaud’s phenomenon and systemic sclerosis. 666
Iloprost treatment in patients with Raynaud’s phenomenon secondary to systemic sclerosis and the quality of life: a new therapeutic protocol. 666
Oral iloprost in Raynaud’s phenomenon secondary to systemic sclerosis: a multicentre, placebo-controlled, dose-comparison study. 666
Second-line therapies 666
Oral vasodilators for primary Raynaud’s phenomenon. 666
Treatment of Raynaud’s phenomenon with the selective serotonin reuptake inhibitor fluoxetine. 666
Successful treatment of patients with severe secondary Raynaud’s phenomenon with the endothelin receptor antagonist bosentan. 666
Effect of the dual endothelin receptor antagonist bosentan on Raynaud’s phenomenon secondary to systemic sclerosis: a double-blind prospective, randomized, placebo-controlled pilot study. 667
Losartan therapy for Raynaud’s phenomenon and scleroderma: clinical and biochemical findings in a fifteen-week, randomized, parallel group, controlled trial. 667
Phosphodiesterase inhibitors in Raynaud’s phenomenon. 667
Efficacy of tadalafil in secondary Raynaud’s phenomenon resistant to vasodilator therapy: a double-blind randomized cross-over trial. 667
A double-blind randomized placebo controlled trial of Hexopal in primary Raynaud’s disease. 667
Third-line therapies 667
Efficacy evaluation of prostaglandin E1 against placebo in patients with progressive systemic sclerosis and significant Raynaud’s phenomenon. 667
A double-blind controlled trial of low dose acetylsalicylic acid and dipyridamole in the treatment of Raynaud’s phenomenon. 667
Calcitonin gene-related peptide in treatment of severe peripheral vascular insufficiency in Raynaud’s phenomenon. 667
Oral L-arginine can reverse digital necrosis in Raynaud’s phenomenon. 667
Treatment of severe Raynaud’s syndrome by injection of autologous blood pretreated by heating, ozonation, and exposure to ultraviolet light (H-O-U) therapy. 667
Triiodothyronine treatment for Raynaud’s phenomenon: a controlled trial. 667
Helicobactor pylori eradication ameliorates primary Raynaud’s phenomenon. 667
The use of digital artery sympathectomy as a salvage procedure for severe ischemia of Raynaud’s disease and phenomenon. 667
Double-blind, randomised, placebo controlled low laser therapy study in patients with primary Reynaud’s phenomenon. 668
Treatment of primary Raynaud’s syndrome with traditional Chinese acupuncture. 668
Evening primrose oil (Efamol) in the treatment of Raynaud’s phenomenon: a double-blind study. 668
Fish-oil dietary supplementation in patients with Raynaud’s phenomenon: a double blind controlled, prospective study. 668
Use of biofeedback training treatment of Raynaud’s disease and phenomenon. 668
Botulinum toxin in the treatment of Raynaud’s phenomenon: a pilot study. 668
Clinical and objective data on spinal cord stimulation for the treatment of severe Raynaud’s phenomenon. 668
209 Reactive arthritis 669
Management strategy 669
Antibiotic use 669
Other modalities 669
Specific investigations 669
European guideline for the management of sexually acquired reactive arthritis. 669
210 Relapsing polychondritis 673
Relapsing polychondritis. 673
Relapsing polychondritis. Survival and predictive role of early disease manifestations. 673
Otologic manifestations of relapsing polychondritis. Review of literature and report of nine cases. 673
Relapsing polychondritis: systemic and ocular manifestations, differential diagnosis, management, and prognosis. 673
Relapsing polychondritis: prevalence of expiratory CT airway abnormalities. 673
Dermatologic manifestations of relapsing polychondritis. A study of 200 cases at a single center. 674
Association of myelodysplastic syndrome and relapsing polychondritis: further evidence. 674
Cardiovascular involvement in relapsing polychondritis. 674
Neurologic manifestations of connective tissue disease. 674
Renal involvement in relapsing polychondritis. 674
The relapsing polychondritis disease activity index: development of a disease activity score for relapsing polychondritis. 674
Management strategy 674
Specific investigations 675
First-line therapies 675
Treatment of relapsing polychondritis with dapsone. 675
211 Rhinophyma 677
Management strategy 677
Specific investigations 677
Rhinophyma and coexisting occult skin cancers. 677
First-line treatments 677
Triple approach to rhinophyma. 677
Second-line treatments 677
Electrosurgical treatment of rhinophyma. 677
Surgical management of rhinophyma: report of eight patients treated with electrosection. 677
Rhinophyma treated by argon laser. 677
Comparison of CO2 laser and electrosurgery in the treatment of rhinophyma. 677
Carbon dioxide laser treatment of rhinophyma: a review of 124 patients. 677
Spectrum of results after treatment of rhinophyma with the carbon dioxide laser. 678
Excision of rhinophyma with Nd:YAG laser: a new technique. 678
Treatment of rhinophyma with Er:YAG laser. 678
Use of a dual-mode erbium:YAG laser for the surgical correction of rhinophyma. 678
Rhinophyma treated by liquid nitrogen spray cryosurgery. 678
Isotretinoin in the treatment of rosacea and rhinophyma. 678
New surgical adjuncts in the treatment of rhinophyma: the microdebrider and FloSeal™. 678
Surgical treatment of rhinophyma with the Shaw scalpel. 678
Rhinophyma, associated with carcinoma, treated successfully with radiation. 678
Rhinophyma treated with kilovoltage photons. 678
Treatment of rhinophyma with the Versajet Hydrosurgery System. 678
212 Rocky Mountain spotted fever and other rickettsial infections 679
Rickettsial spotted fevers 679
Rocky Mountain spotted fever 679
Management strategy 679
Fatal cases of Rocky Mountain spotted fever in family clusters – three states, 2003. 680
Clinical and laboratory features, hospital course, and outcome of Rocky Mountain spotted fever in children. 680
Specific investigations 680
Laboratory diagnosis of Rocky Mountain spotted fever. 680
A highly sensitive and specific real-time PCR assay for the detection of spotted fever and typhus group Rickettsiae. 680
Identification of rickettsial infections by using cutaneous swab specimens and PCR. 680
First-line therapies 680
Should tetracycline be contraindicated for therapy of presumed RMSF in children less than 9 years of age? 680
Rocky Mountain spotted fever: a clinician’s dilemma. 681
Second-line therapies 681
Analysis of risk factors for fatal Rocky Mountain spotted fever: evidence for superiority of tetracyclines for therapy. 681
Clarithromycin versus azithromycin in the treatment of Mediterranean spotted fever in children: a randomized controlled trial. 681
Third-line therapies 681
Evaluation of the antirickettsial activities of fluoroquinolones. 681
Typhus group 681
Management strategy 681
Epidemic typhus 681
Murine typhus 681
Scrub typhus 681
Specific investigations 681
First-line therapies 681
Comparison of the effectiveness of five different antibiotic regimens on infection with Rickettsia typhi: therapeutic data from 87 cases. 682
Doxycycline and rifampicin for mild scrub-typhus infections in northern Thailand: a randomized trial. 682
Doxycycline versus azithromycin for treatment of leptospirosis and scrub typhus. 682
Murine typhus in central Greece: epidemiological, clinical, laboratory, and therapeutic-response features of 90 cases. 682
Rickettsialpox 682
213 Rosacea 684
Management strategy 684
Specific investigations 684
Inflammatory rosacea 684
First-line treatments 684
Treatment of rosacea with 1% metronidazole cream. 684
The efficacy of metronidazole 1% cream once daily compared with metronidazole cream twice daily and their vehicles in rosacea: a double-blind clinical trial. 684
Topical metronidazole maintains remissions of rosacea. 684
A randomized, double-blind, placebo-controlled trial of the combined effect of doxycycline hyclate 20 mg tablets and metronidazole 0.75% topical lotion in the treatment of rosacea. 684
Topical azelaic acid in the treatment of rosacea. 685
Double-blind comparison of azelaic acid 20% cream and its vehicle in treatment of papulo-pustular rosacea. 685
A comparison of 15% azelaic acid gel and 0.75% metronidazole gel in the topical treatment of papulopustular rosacea. 685
A clinical trial of tetracycline in rosacea. 685
Safety of long-term tetracycline therapy for acne. 685
Two randomized phase III clinical trials evaluating anti-inflammatory dose doxycycline (40-mg doxycycline, USP capsules) administered once daily for treatment of rosacea. 685
A double-blind study of 1% metronidazole cream versus systemic oxytetracycline therapy for rosacea. 685
Steroid rosacea in prepubertal children. 685
Beneficial use of Cetaphil moisturizing cream as part of a daily skin care regimen for individuals with rosacea. 685
Second-line treatments 685
Topically applied erythromycin in rosacea. 685
Treatment of rosacea: topical clindamycin versus oral tetracycline. 685
Double-blind, randomized, vehicle-controlled clinical trial of once-daily benzoyl peroxide/clindamycin topical gel in the treatment of patients with moderate to severe rosacea. 685
Treatment of rosacea by metronidazole. 685
A double-blinded trial of metronidazole versus oxytetracycline therapy for rosacea. 685
Topical treatment of acne rosacea with benzoyl peroxide acetone gel. 686
Comparative effectiveness of tetracycline and ampicillin in rosacea. A controlled trial. 686
A novel treatment for acne vulgaris and rosacea. 686
Therapeutic potential of azithromycin in rosacea. 686
Oral use of azithromycin for the treatment of acne rosacea. 686
Third-line treatments 686
Treatment of rosacea with isotretinoin. 686
Continuous microdose isotretinoin in adult recalcitrant rosacea. 686
Topical tretinoin for rosacea; a preliminary report. 686
Adapalene vs. metronidazole gel for the treatment of rosacea. 686
Topical treatment with sulfur 10% for rosacea. 686
The treatment of rosacea: the safety and efficacy of sodium sulfacetamide 10% and sulfur 5% lotion (Novacet) is demonstrated in a double-blind study. 686
Comparative study of triamcinolone acetonide and hydrocortisone 17-butyrate in rosacea with special regard to the rebound phenomenon. 686
Treatment of rosacea with ketoconazole. 687
Treatment of rosacea with bifonazole cream: a preliminary report. 687
Photodynamic therapy in a series of rosacea patients. 687
Oral spironolactone therapy in male patients with rosacea. 687
Demodex folliculorum and topical treatment: action evaluated by standardized skin surface biopsy. 687
A pilot study of 5% permethrin cream versus 0.75% metronidazole gel in acne rosacea. 687
Permethrin 5% cream versus metronidazole 0.75% gel for the treatment of papulopustular rosacea. A randomized double-blind placebo-controlled study. 687
Treatment of rosacea-like demodicidosis with oral ivermectin and topical permethrin cream. 687
A study on Demodex folliculorum in rosacea. 687
Helicobacter pylori eradication treatment reduces the severity of rosacea. 687
The response of rosacea to eradication of Helicobacter pylori. 687
The effect of the treatment of Helicobacter pylori infection on rosacea. 687
Effective sunscreen ingredients and cutaneous irritation in patients with rosacea. 687
Tacrolimus ointment for the treatment of steroid-induced rosacea: a preliminary report. 687
Tacrolimus effect on rosacea. 687
Pimecrolimus for treatment of acne rosacea. 687
Pimecrolimus cream 1% for papulopustular rosacea: a randomized vehicle-controlled double-blind trial. 688
Incidental control of rosacea by somatostatin. 688
Effect of oral inhibitors of ovulation in treatment of rosacea and dermatitis perioralis in women. 688
Topical application of NADH for the treatment of rosacea and contact dermatitis. 688
Topical application of 1-methylnicotinamide in the treatment of rosacea: a pilot study. 688
The Nicomide Improvement in Clinical Outcomes Study (NICOS): results of an 8-week trial. 688
Oral zinc sulfate in the treatment of rosacea: a double-blind, placebo-controlled study. 688
Low-strength trichloroacetic acid in the treatment of rosacea. 688
Erythematotelangiectatic rosacea 688
First-line therapies 688
Once-daily topical brimonidine tartrate gel 0.5% is a novel treatment for moderate to severe facial erythema of rosacea: results of two multicentre, randomized and vehicle-controlled studies. 688
Successful treatment of the erythema and flushing of rosacea using a topically applied selective alpha1-adrenergic receptor agonist, oxymetazoline. 688
Decorative cosmetics improve the quality of life in patients with disfiguring skin diseases. 688
Objective and quantitative improvement of rosacea- associated erythema after intense pulsed light treatment. 688
Treatment of rosacea with intense pulsed light. 689
Treatment of facial vascular lesions with intense pulsed light. 689
Argon laser treatment of the red nose. 689
Flash lamp pumped dye laser for rosacea-associated telangiectasia and erythema. 689
Pulsed dye laser therapy for rosacea. 689
How laser surgery can help your rosacea patients. 689
Hair dryer use to optimize pulsed dye laser treatment in rosacea patients. 689
The response of erythematous rosacea to ondansetron. 689
Rosacea flushing 689
First-line therapies 689
Clonidine and facial flushing in rosacea. 689
Flushing in rosacea: a possible mechanism. 689
Effect of subdepressor clonidine on flushing reactions in rosacea. Change in malar thermal circulation index during provoked flushing reactions. 689
Rilmenidine in rosacea: a double-blind study versus placebo. 689
Effect of nadolol on flushing reactions in rosacea. 689
Alcohol-induced rosacea flushing blocked by naloxone. 690
Hypnosis in dermatology. 690
Influence of the 5-HT3 receptor antagonist granisetron on erythema and flushing tendency in rosacea patients. 690
Rosacea lymphedema (morbihan’s disease) 690
214 Sarcoidosis 692
Management strategy 692
Specific investigations 692
Sarcoidosis. 692
Sarcoidosis: a comprehensive review and update for the dermatologist – Part I. Cutaneous disease. 692
First-line therapies 693
Verrucous cutaneous sarcoidosis in an adolescent with dark skin. 693
A case of scar sarcoidosis of the eyelid. 693
Evidence-based therapy for cutaneous sarcoidosis. 693
Treatment of cutaneous sarcoidosis with chloroquine: review of the literature. 693
Hydroxychloroquine is effective therapy for control of cutaneous sarcoidal granulomas. 693
Methotrexate is steroid sparing in acute sarcoidosis: results of a double blind, randomized trial. 693
Prolonged use of methotrexate for sarcoidosis. 693
Second-line therapies 693
Mycophenolate mofetil may serve as a steroid-sparing agent for sarcoidosis. 693
Treatment of lupus pernio: The results of 116 treatment courses in 54 patients. 693
Treatment of sarcoidosis with infliximab. 694
The use of tetracyclines for the treatment of sarcoidosis. 694
Third-line therapies 694
Treatment of cutaneous sarcoidosis with thalidomide. 694
A case of cutaneous acral sarcoidosis with response to allopurinol. 694
Cutaneous sarcoidosis: complete remission after oral isotretinoin therapy. 694
Long-term use of azathioprine as a steroid-sparing treatment. 694
Chlorambucil treatment of sarcoidosis. 694
Scar sarcoidosis following tattooing of the lips treated with mepacrine. 694
Successful treatment of recalcitrant cutaneous sarcoidosis with fumaric acid esters. 695
Lichenoid type of cutaneous sarcoidosis: great response to topical tacrolimus. 695
Intralesional chloroquine for the treatment of cutaneous sarcoidosis. 695
Cutaneous nasal sarcoidosis: treatment by excision and split-skin grafting. 695
CO2 laser vaporization for disfiguring lupus pernio. 695
Scar sarcoidosis in a child: case report of successful treatment with the pulsed dye laser. 695
Successful treatment of cutaneous sarcoidosis lesions with the flashlamp pumped pulsed dye laser: A case report. 695
Melatonin is a safe and effective treatment for chronic pulmonary and extrapulmonary sarcoidosis. 695
Efficacy and safety of apremilast in chronic cutaneous sarcoidosis. 695
Leflunomide for chronic sarcoidosis. 695
Adalimumab for treatment of cutaneous sarcoidosis. 695
Cutaneous sarcoidosis treated with medium-dose UVA1. 695
Treatment of cutaneous sarcoid with topical gel psoralen and ultraviolet A. 695
Photodynamic therapy for the treatment of cutaneous sarcoidosis. 696
Cutaneous sarcoid mimicking tinea imbricata. 696
215 Scabies 697
Epidemiology of scabies prevalence in the U.K. from general practice records. 697
Management strategy 697
Specific investigations 697
Epiluminescence microscopy. A new approach to in vivo detection of Sarcoptes scabiei. 697
‘Wake sign’: an important clue for the diagnosis of scabies. 698
The burrow ink test and the scabies mite. 698
A diagnostic test for scabies: IgE specificity for a recombinant allergen of Sarcoptes scabiei. 698
First-line therapies 698
Permethrin 5% dermal cream: a new treatment for scabies. 698
Sarcoptes scabiei infestation treated with malathion liquid. 698
A family based study on the treatment of scabies with benzyl benzoate and sulphur ointment. 698
Interventions for treating scabies. 698
Ivermectin versus benzyl benzoate applied once or twice to treat human scabies in Dakar, Senegal: a randomized controlled trial. 698
Second-line therapies 698
Therapeutic efficacy, secondary effects, and patient acceptability of 10% sulfur in either pork fat or cold cream for the treatment of scabies. 698
Permethrin versus crotamiton and lindane in the treatment of scabies. 698
Comparison of crotamiton 10% cream (Eurax) and permethrin 5% cream (Elimite) for the treatment of scabies in children. 698
Tratamiento de la escabiasis con ivermectina por via oral. 698
Comparison of ivermectin and benzyl benzoate for treatment of scabies. 698
Treatment of scabies with ivermectin. 699
Variable response of crusted scabies to oral ivermectin: report on eight Egyptian patients. 699
A comparative trial of oral ivermectin and topical permethrin in the treatment of scabies. 699
Safety of and compliance with community-based ivermectin therapy. 699
Adverse reactions after large-scale treatment of onchocerciasis with ivermectin: combined results from eight community trials. 699
Deaths associated with ivermectin treatment of scabies. 699
Third-line therapies 699
Control of scabies by use of soap impregnated with tetra-ethylthiuram monosulphide (‘tetmosol’). 699
Scabies prophylaxis using ‘tetmosol’ soap. 699
Topically applied thiabendazole in the treatment of scabies. 699
A trial of co-trimoxazole in scabies. 699
Efficacy and tolerability of natural synergised pyrethrins in a new thermolabile foam formulation in topical treatment of scabies: a prospective randomized, investigator-blinded, comparative trial vs permethrin cream. 699
216 Scleredema 700
Management strategy 700
Scleredema: a review of thirty cases. 700
Mucinoses (Chapter 46). 700
Specific investigations 700
Scleredema adultorum due to streptococcal infection. 700
Monoclonal gammopathy in scleredema: observations in three cases. 700
Scleredema associated with carcinoma of the gall bladder. 700
Scleredema and diabetes mellitus. 700
First-line therapies 700
Scleredema: a review of thirty-three cases. 701
Scleredema adultorum. Not always a benign self-limited disease. 701
Second-line therapies 701
Scleredema adultorum treated with narrow-band ultraviolet B phototherapy. 701
UVA1 phototherapy for cutaneous diseases: an experience of 92 cases in the United States. 701
Scleredema diabeticorum case series: successful treatment with UV-A1. 701
Scleredema diabeticorum successfully treated with ultraviolet A1 phototherapy. 701
Scleredema treated with broad-band ultraviolet A phototherapy plus colchicine. 701
Scleredema of Buschke successfully treated with electron beam therapy. 701
Electron-beam therapy in scleredema adultorum with associated monoclonal hypergammaglobulinaemia. 701
Bath-PUVA therapy in three patients with scleredema adultorum. 701
Cream PUVA therapy for scleredema adultorum. 702
Ultrasonic massage and physical therapy for scleredema: improving activities of daily living. 702
Treatment of scleredema diabeticorum with tamoxifen. 702
Persistent scleredema of Buschke in a diabetic: improvement with high-dose penicillin. 702
Cylcosporine in scleredema. 702
Scleredema associated with paraproteinemia treated by extracorporeal photopheresis. 702
Beneficial effect of aggressive low-density lipoprotein apheresis in a familial hypercholesterolemic patient with severe diabetic scleredema. 702
Treatment with chemotherapy of scleredema associated with IgA myeloma. 702
217 Scleroderma 703
Management strategy 703
Specific investigations 703
Evidence-based guidelines for the use of immunologic tests: anticentromere, Scl-70, and nucleolar antibodies. 703
Scleroderma: clinical and pathological advances. 703
First-line therapies 703
Iloprost for the treatment of systemic sclerosis. 704
Calcium channel blockers for Raynaud’s phenomenon. 704
Outcome of renal crisis in systemic sclerosis: relation to availability of angiotensin converting enzyme (ACE) inhibitors. 704
Second-line therapies 704
Evaluation of oral methotrexate in the treatment of systemic sclerosis. 704
Randomized placebo controlled trial of methotrexate in systemic sclerosis. 704
A randomized, controlled trial of methotrexate versus placebo in early diffuse scleroderma. 704
The efficacy of oral cyclophosphamide plus prednisolone in early diffuse systemic sclerosis. 704
Randomized unblinded trial of cyclophosphamide versus azathioprine in the treatment of systemic sclerosis. 704
Efficacy and safety of intravenous cyclophosphamide pulse therapy with oral prednisolone in the treatment of interstitial lung disease with systemic sclerosis: 4-year follow-up. 704
Treatment of early diffuse cutaneous systemic sclerosis patients in Japan by low-dose corticosteroids for skin involvement. 704
The vitamin A derivative etretinate improves skin sclerosis in patients with systemic sclerosis. 704
Losartan therapy for Raynaud’s phenomenon and scleroderma: clinical and biochemical findings in a fifteen-week, randomized, parallel-group, controlled trial. 704
Therapeutic management of acral manifestations of systemic sclerosis. 705
Long-term evaluation of colchicine in the treatment of scleroderma. 705
Different low doses of broad-band UVA in the treatment of morphea and systemic sclerosis. 705
Effect of mycophenolate sodium in scleroderma-related interstitial lung disease. 705
A prospective open-label study of mycophenolate mofetil for the treatment of diffuse systemic sclerosis. 705
Third-line therapies 705
Systemic Sclerosis Study Group. A randomized, double-blind, placebo-controlled trial of photopheresis in systemic sclerosis. 705
Imatinib mesylate (Gleevec) in the treatment of diffuse cutaneous systemic sclerosis: results of a 1-year, phase IIa, single-arm, open-label clinical trial. 705
Cyclosporine in systemic sclerosis. 705
B cell depletion in diffuse progressive systemic sclerosis: safety, skin score modification and IL-6 modulation in an up to thirty-six months follow-up open-label trial. 705
Autologous non-myeloablative haemopoietic stem-cell transplantation compared with pulse cyclophosphamide once per month for systemic sclerosis (ASSIST): an open-label, randomised phase 2 trial. 705
Immune stimulation in scleroderma patients treated with thalidomide. 705
Reduced fibrosis and normalisation of skin structure in scleroderma patients treated with thalidomide. 706
Etanercept as treatment for diffuse scleroderma: a pilot study. 706
Minocycline in early diffuse scleroderma. 706
Minocycline is not effective in systemic sclerosis: results of an open-label multicenter trial. 706
Other: internal organ involvement 706
Prostacyclin for pulmonary hypertension in adults. 706
Review of bosentan in the management of pulmonary arterial hypertension. 706
Bosentan therapy for pulmonary arterial hypertension. 706
Interstitial lung disease associated with systemic sclerosis: what is the evidence for efficacy of cyclophosphamide? 706
Cyclophosphamide is associated with pulmonary function and survival benefit in patients with scleroderma and alveolitis. 706
Renal transplantation in scleroderma. 706
Omeprazole in the long-term treatment of severe gastro-oesophageal reflux disease in patients with systemic sclerosis. 706
218 Sebaceous hyperplasia 707
Management strategy 707
Specific investigations 707
Alta prevalencia de hiperplasias sebaceas en transplantados renales. 707
First-line therapies 707
Surgical pearl: intralesional electrodesiccation of sebaceous hyperplasia. 707
Guidelines of care for cryosurgery. 707
Second-line therapies 707
Successful treatment of cyclosporine-induced sebaceous hyperplasia with oral isotretinoin in two renal transplant recipients. 707
Premature familial sebaceous hyperplasia: successful response to oral isotretinoin in three patients. 707
Isotretinoin for the treatment of sebaceous hyperplasia. 707
Photodynamic therapy of sebaceous hyperplasia with topical 5-aminolaevulenic acid and slide projector. 707
Treatment of sebaceous gland hyperplasia by photodynamic therapy with 5-aminolevulinic acid and a blue light source or intense pulsed light source. 708
Third-line therapies 708
Photodynamic therapy with topical aminolevulenic acid and pulsed dye laser irradiation for sebaceous hyperplasia. 708
Sebaceous hyperplasia treated with a 1450-nm diode laser. 708
Elucidating the pulsed-dye laser treatment of sebaceous hyperplasia in vivo with real-time confocal scanning laser microscopy. 708
A three year experience with the argon laser in dermatotherapy. 708
Sebaceous gland hyperplasia as a side effect of cyclosporin A. Treatment with the CO2 laser. 708
Controlled cosmetic dermal ablation in the facial region with the erbium:YAG laser. 708
The treatment of benign sebaceous hyperplasia with the topical application of bichloracetic acid. 708
Surgical removal 708
219 Seborrheic eczema 709
Management strategy 709
Specific investigations 709
New insights into HIV-1-primary skin disorders. 709
Seborrheic dermatitis in neuroleptic-induced Parkinsonism. 709
Cutaneous changes in chronic alcoholics. 709
Non-scalp disease 709
First-line therapies 709
Ketoconazole 2% cream versus hydrocortisone 1% cream in the treatment of seborrhoeic dermatitis. A double-blind comparative study. 709
Comparative study of ketoconazole 2% foaming gel and betamethasone dipropionate 0.05% lotion in the treatment of seborrhoeic dermatitis in adults. 709
Randomised double blind controlled trial of 2% ketoconazole cream versus 0.05% clobetasol 17-butyrate cream in seborrhoeic dermatitis. 710
A novel foam formulation of ketoconazole 2% for the treatment of seborrheic dermatitis on multiple body regions. 710
Second-line therapies 710
A double-blind, placebo-controlled, multicenter trial of lithium succinate ointment in the treatment of seborrhoeic dermatitis. 710
Lithium gluconate 8% vs ketoconazole 2% in the treatment of seborrhoeic dermatitis: a multicentre, randomized study. 710
Randomized, placebo-controlled, double-blind study on clinical efficacy of ciclopiroxolamine 1% cream in facial seborrhoeic dermatitis. 710
Pimecrolimus 1% cream, methylprednisolone aceponate 0.1% cream and metronidazole 0.75% gel in the treatment of seborrhoea dermatitis: a randomized clinical study. 710
Single-blind, randomized controlled trial evaluating the treatment of facial seborrheic dermatitis with hydrocortisone 1% ointment compared with tacrolimus 0.1% ointment in adults. 710
Third-line therapies 710
Oral terbinafine in the treatment of multi-site seborrheic dermatitis: a multicentre, double-blind placebo-controlled study. 710
Oral itraconazole for the treatment of seborrhoeic dermatitis: an open, non-comparative trial. 710
Metronidazole 0.75% gel vs. ketoconazole 2% cream in the treatment of facial seborrheic dermatitis: a randomized, double blind study. 710
An investigator-blind, randomized, 4-week, parallel-group, multicenter pilot study to compare the safety and efficacy of a nonsteroidal cream (Promiseb Topical Cream) and desonide cream 0.05% in the twice-daily treatment of mild to moderate seborrheic dermatitis of the face. 711
Narrow-band ultraviolet B (TL-01) phototherapy is an effective and safe treatment option for patients with severe seborrhoeic dermatitis. 711
Benzoyl peroxide in seborrheic dermatitis. 711
Efficacy of terbinafine 1% cream on seborrheic dermatitis. 711
Scalp disease 711
First-line therapies 711
Successful treatment and prophylaxis of scalp seborrhoeic dermatitis and dandruff with 2% ketoconazole shampoo: results of a multicentre, double-blind, placebo-controlled trial. 711
Treatment and prophylaxis of seborrheic dermatitis of the scalp with antipityrosporal 1% ciclopirox shampoo. 711
Clinical efficacies of shampoos containing ciclopirox olamine (1.5%) and ketoconazole (2%) in the treatment of seborrheic dermatitis. 711
A multicenter randomized trial of ketoconazole 2% and zinc pyrithione 1% shampoos in severe dandruff and seborrheic dermatitis. 711
Second-line therapies 711
Propylene glycol in the treatment of seborrhoeic dermatitis of the scalp: a double-blind study. 711
A randomized, double-blind, placebo-controlled trial of ketoconazole 2% shampoo versus selenium sulfide 2.5% shampoo in the treatment of moderate to severe dandruff. 711
Seborrhoeic dermatitis and Pityrosporum orbiculare: treatment of seborrhoeic dermatitis of the scalp with miconazole-hydrocortisone (Daktacort), miconazole and hydrocortisone. 711
Clinical efficacies of topical agents for the treatment of seborrheic dermatitis of the scalp: a comparative study. 712
Efficacy of betamethasone valerate 0.1% thermophobic foam in seborrhoeic dermatitis of the scalp: an open-label, multicentre, prospective trial on 180 patients. 712
Efficacious and safe management of moderate to severe scalp seborrhoeic dermatitis using clobetasol propionate shampoo 0.05% combined with ketoconazole shampoo 2%: a randomized, controlled study. 712
220 Seborrheic keratosis 713
Management strategy 713
Seborrheic keratosis variants 713
Multiple seborrheic keratoses 713
Specific investigations 713
Sign of Leser–Trelat. 713
First-line therapies 714
Curettage of small basal cell papillomas with the disposable ring curette is superior to conventional treatment. 714
Skin tumours: seborrhoeic warts. 714
Cutaneous cryotherapy: principles and practice. 714
Treatment of superficial surgical wounds after removal of seborrhoeic keratoses: a single-blinded randomized- controlled study. 714
Second-line therapies 714
Focal trichloroacetic acid peel method for benign pigmented lesions in dark-skinned patients. 714
Use of the alexandrite laser for treatment of seborrhoeic keratoses. 714
Use of a long-pulse alexandrite laser in the treatment of superficial pigmented lesions. 714
Treatment of verruca vulgaris, seborrheic keratoses, lentigines, and actinic cheilitis. Clinical advantage of the CO2 laser superpulsed mode. 714
Ablation of cutaneous lesions using an erbium:YAG laser. 714
532-nm diode laser treatment of seborrhoeic keratoses with color enhancement. 714
Third-line therapies 714
Giant seborrhoeic keratosis on the frontal scalp treated with topical fluorouracil. 714
Seborrhoeic keratoses: a study comparing the standard cryosurgery with topical calcipotriene, topical tazorotene and topical imiquimod. 714
Use of a keratolytic agent with occlusion for topical treatment of hyperkeratotic seborrhoeic keratoses. 714
221 Sporotrichosis 715
Management strategy 715
Specific investigations 715
Disseminated sporotrichosis and Sporothrix schenckii fungemia as the initial presentation of human immunodeficiency virus infection. 715
Potassium iodide in dermatology: a 19th century drug for the 21st century: uses, pharmacology, adverse effects, and contraindications. 715
Disseminated sporotrichosis associated with treatment with immunosuppressants and tumor necrosis factor-alpha antagonists. 715
Disseminated sporotrichosis as a manifestation of immune reconstitution inflammatory syndrome. 716
Sporotrichosis. 716
First-line therapies 716
Treatment of cutaneous sporotrichosis with itraconazole: study of 645 patients. 716
Efficacy and safety of itraconazole pulses vs. continuous regimen in cutaneous sporotrichosis. 716
Cutaneous sporotrichosis in Himachal Pradesh, India. 716
Sporotrichosis in childhood: clinical and therapeutic experience in 25 patients. 716
Comparative evaluation of the efficacy and safety of two doses of terbinafine (500 and 1000 mg/day) in the treatment of cutaneous or lymphocutaneous sporotrichosis. 716
Terbinafine (250 mg/day): an effective and safe treatment of cutaneous sporotrichosis. 716
Comparative study of 250 mg/day terbinafine and 100 mg/day itraconazole for the treatment of cutaneous sporotrichosis. 716
Cutaneous and meningeal sporotrichosis in a HIV patient. 717
Second-line therapies 717
A Pan-American 5-year study of fluconazole therapy for deep mycoses in the immunocompetent host. Pan-American Study Group. 717
Treatment of lymphocutaneous and visceral sporotrichosis with fluconazole. 717
Hyperthermic treatment of sporotrichosis: experimental use of infrared and far infrared rays. 717
Cryosurgery as adjuvant therapy in cutaneous sporotrichosis. 717
Guidelines 717
Clinical practice guidelines for the management of sporotrichosis: 2007 Update by the Infectious Diseases Society of America. 717
222 Squamous cell carcinoma 718
Management strategy 718
Specific investigations 718
Surgical pearl: obtaining a clean histopathologic specimen using a ring curette. 719
Reliability of the histopathologic diagnosis of keratinocyte carcinomas. 719
Predictive value of margins in diagnostic biopsies of nonmelanoma skin cancers. 719
Epidermal growth factor receptor: a novel biomarker for aggressive head and neck cutaneous squamous cell carcinoma. 719
RAS mutations in cutaneous squamous-cell carcinomas in patients treated with BRAF inhibitors. 719
High-risk cutaneous squamous cell carcinoma without palpable lymphadenopathy: is there a therapeutic role for elective neck dissection? 719
Sentinel lymph node biopsy for high risk cutaneous squamous cell carcinoma: case series and review of the literature. 719
Role of neck ultrasound during follow-up care of head and neck squamous cell carcinomas. 719
First-line therapies 719
Advanced cancer of the extremities treated by cryosurgery. 719
Controversies in skin surgery: electrodessication and curettage versus excision for low-risk, small, well-differentiated squamous cell carcinomas. 719
The occurrence of residual or recurrent squamous cell carcinomas in organ transplant recipients after curettage and electrodesiccation. 720
Prospective trial of curettage and cryosurgery in the management of non-facial, superficial, and minimally invasive basal and squamous cell carcinoma. 720
Surgical margins for excision of primary squamous cell carcinoma. 720
Surgical margins of excision for basal cell carcinoma and squamous cell carcinoma. 720
Cutaneous squamous cell carcinoma treated with Mohs micrographic surgery in Australia I. Experience over 10 years. 720
Cutaneous squamous cell carcinoma treated with Mohs micrographic surgery in Australia II. Perineural invasion. 720
Recurrence after treatment of nonmelanoma skin cancer: a prospective cohort study. 720
Office-based radiation therapy for cutaneous carcinoma: evaluation of 710 treatments. 720
The use of brachytherapy in the treatment of nonmelanoma skin cancer: a review. 720
Second-line therapies 720
Imiquimod 5% cream in the treatment of Bowen’s disease and invasive squamous cell carcinoma. 720
Topical imiquimod or fluorouracil therapy for basal and squamous cell carcinoma: a systematic review. 721
Electrochemotherapy in primary and metastatic skin tumors: phase II trial using intralesional bleomycin. 721
Intralesional interferon alpha-2b in the treatment of basal cell carcinoma and squamous cell carcinoma: revisited. 721
Intralesional methotrexate treatment for keratoacanthoma tumors: a retrospective study and review of the literature. 721
Intralesional chemotherapy for nonmelanoma skin cancer: a practical review. 721
Intralesional agents in the management of cutaneous malignancy: a review. 721
Third-line therapies 721
Squamous cell carcinoma arising in osteomyelitis and chronic wounds. Treatment with Mohs’ micrographic surgery vs. amputation. 721
Methyl-aminolevulinate photodynamic therapy for the treatment of actinic keratoses and non-melanoma skin cancers: a retrospective analysis of response in 462 patients. 721
A review of laser and photodynamic therapy for the treatment of nonmelanoma skin cancer. 721
Acitretin suppression of squamous cell carcinoma: case report and literature review. 721
Oral retinoid use reduces cutaneous squamous cell carcinoma risk in patients with psoriasis treated with psoralen-UVA: a nested cohort study. 722
Systemic retinoids for chemoprevention of non-melanoma skin cancer in high-risk patients. 722
Phase II study of cetuximab as first-line single-drug therapy in patients with unresectable squamous cell carcinoma of the skin. 722
The promise of molecular targeted therapies: protein kinase inhibitors in the treatment of cutaneous malignancies. 722
Chemoradiation using low-dose cisplatin and 5- fluorouracil in locally advanced squamous cell carcinoma of the skin: a report of two cases. 722
223 Staphylococcal scalded skin syndrome 723
Management strategy 723
Early hospital discharge and cross-infection. 723
Nosocomial outbreak of staphylococcal scalded skin syndrome in neonates: epidemiological investigation and control. 723
Specific Investigations 723
Isolating Staphylococcus aureus from children with suspected staphylococcal scalded skin syndrome is not clinically useful. 724
First-line therapies 724
Outbreak of staphylococcal scalded skin syndrome among neonates. 724
Mild staphylococcal scalded skin syndrome: an underdiagnosed clinical disorder. 724
Staphylococcal scalded skin syndrome in healthy adults. 724
Staphylococcal scalded skin syndrome as a complication of septic arthritis. 724
Second-line therapies 724
A clinical and microbiological comparison of Staphylococcus aureus toxic shock and scalded skin syndromes in children. 724
Staphylococcal scalded skin syndrome in the course of lupus nephritis. 724
Staphylococcal scalded skin syndrome in an adult due to methicillin-resistant Staphylococcus aureus. 724
Third-line therapies 724
Antimicrobial agent of susceptibilities and antiseptic resistance gene distribution among methicillin-resistant Staphylococcal aureus isolates from patients with impetigo and staphylococcal scalded skin syndrome. 724
Staphylococcal scalded skin syndrome in two very low birth weight infants. 724
Adult staphylococcus scalded skin syndrome in a peritoneal dialysis patient. 724
Staphylococcal scalded skin syndrome caused by exfoliative toxin B-producing methicillin-resistant Staphylococcus aureus. 725
Staphylococcal scalded skin syndrome in an extremely premature neonate: a case report with a brief review of the literature. 725
Severe staphylococcal scalded skin syndrome in children. 725
An innovative local treatment for staphylococcal scalded skin syndrome. 725
Use of skin substitute dressings in the treatment of staphylococcal scalded skin syndrome in neonates and young infants. 725
224 Steatocystoma multiplex 726
Management strategy 726
Specific investigations 726
A novel mutation (p.Arg94Gly) of keratin 17 in a Chinese family with steatocystoma multiplex. 726
Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation. 726
First-line therapies 726
Steatocystoma multiplex suppurativum: treatment with isotretinoin. 726
The treatment of steatocystoma multiplex suppurativum with isotretinoin. 726
Isotretinoin in the treatment of steatocystoma multiplex: a possible adverse reaction. 726
Steatocystoma multiplex treated with isotretinoin: a delayed response. 726
Treatment of steatocystoma multiplex and pseudofolliculitis barbae with isotretinoin. 726
Successful treatment of steatocystoma multiplex by simple surgery. 726
Five generations with steatocystoma multiplex congenita: a treatment regimen. 726
Surgical pearl: mini-incisions for the extraction of steatocystoma multiplex. 726
A simple surgical technique for the treatment of steatocystoma multiplex. 726
Suggestion for the treatment of steatocystoma multiplex located exclusively on the face. 727
The vein hook successfully used for eradication of steatocystoma multiplex. 727
Perforation and extirpation of steatocystoma multiplex. 727
Second-line therapies 727
CO2 laser therapy for steatocystoma multiplex. 727
1450-nm Diode laser in combination with the 1550-nm fractionated erbium-doped fiber laser for the treatment of steatocystoma multiplex: a case report. 727
Third-line therapies 727
Treatment of lesions of steatocystoma multiplex and other epidermal cysts by cryosurgery. 727
225 Stoma care 728
Management strategy 728
Specific investigations 728
The spectrum of skin disorders in abdominal stoma patients. 728
Stoma-related complications and stoma size - a 2-year follow up. 728
A prospective audit of stomas – analysis of risk factors and complications and their management. 728
The relevance of patch testing in peristomal dermatitis. 729
First-line therapies 729
Dermatologic considerations of stoma care. 729
Peristomal dermatoses: a novel indication for topical steroid lotions. 729
Topical therapy for peristomal pyoderma gangrenosum (PPG). 729
Second-line therapies 729
Topical sucralfate in the management of peristomal skin disease: an open study. 729
Peristomal pyoderma gangrenosum. 729
Topical tacrolimus in the management of peristomal pyoderma gangrenosum. 729
Third-line therapies 729
Clinical features and treatment of peristomal pyoderma gangrenosum (PPG). 729
Management of peristomal pyoderma gangrenosum. 729
Paraileostomy recontouring by collagen sealant injection: a novel approach to one aspect of ileostomy morbidity. Report of a case. 729
Troublesome colostomies and urinary stomas treated with suction assisted lipectomy. 729
Synchronous panniculectomy with stomal revision for obese patients with stomal stenosis and retraction. 729
226 Striae 730
Management strategy 730
Specific investigations 730
First-line therapies 730
Adolescent striae. 730
Striae cutis distensae. 730
Second-line therapies 730
Treatment of striae distensae using an ablative 10,600-nm carbon dioxide fractional laser: a retrospective review of 27 participants. 730
The effect of succinylated atelocollagen and ablative fractional resurfacing laser on striae distensae. 731
Treatment of striae distensae with nonablative fractional laser versus ablative CO2 fractional laser: a randomized controlled trial. 731
Treatment of striae distensae with fractional photothermolysis. 731
Treatment of striae rubra and striae alba with the 585-nm pulsed-dye laser. 731
Topical tretinoin 0.1% for pregnancy-related abdominal striae: an open-label, multicenter, prospective study. 731
Third-line therapies 731
The 308-nm excimer laser in the darkening of the white lines of striae alba. 731
Intense pulsed light in the treatment of striae distensae. 731
Two-year follow-up results of copper bromide laser treatment of striae. 731
Stretch marks: treatment using the 1064-nm Nd : YAG laser. 731
Radiofrequency and 585-nm pulsed dye laser treatment of striae distensae: a report of 37 Asian patients. 731
Treatment of striae distensae with a TriPollar radiofrequency device: a pilot study. 731
Prospective clinical and histological study to evaluate the efficacy and safety of a targeted high-intensity narrow band UVB/UVA1 therapy for striae alba. 732
A superficial texture analysis of 70% glycolic acid topical therapy and striae distensae. 732
Comparison of topical therapy for striae alba (20% glycolic acid/0.05% tretinoin versus 20% glycolic acid/10% L-ascorbic acid). 732
Chemical peel of nonfacial skin using glycolic acid gel augmented with TCA and neutralized based on visual staging. 732
Prophylaxis of striae gravidarum with a topical formulation: a double blind trial. 732
Laser therapy of stretch marks. 732
227 Subacute cutaneous lupus erythematosus 733
Management strategy 733
Specific investigations 733
Drug-induced, Ro/SSA-positive cutaneous lupus erythematosus. 733
Subacute cutaneous lupus erythematosus and its association to drugs: a population-based matched case-control study of 234 patients in Sweden. 733
A systematic review of drug-induced subacute cutaneous lupus erythematosus. 733
Report of an association between discoid lupus erythematosus and smoking. 734
Patients with cutaneous lupus erythematosus who smoke are less responsive to antimalarial treatment. 734
Clinical and pharmacogenetic influences on response to hydroxychloroquine in discoid lupus erythematosus: a retrospective cohort study. 734
Impact of smoking in cutaneous lupus erythematosus. 734
First-line therapies 734
Experimental reproduction of skin lesions in lupus erythematosus by UVA and UVB radiation. 734
Evaluation of the capacity of sunscreens to photoprotect lupus erythematosus patients by employing the photoprovocation test. 734
Intralesional triamcinolone is effective for discoid lupus erythematosus of the palms and soles. 734
The association of the two antimalarials chloroquine and quinacrine for treatment-resistent chronic and subacute cutaneous lupus erythematosus. 734
Hydroxychloroquine sulfate treatment is associated with later onset of systemic lupus erythematosus. 734
Cutaneous lupus treated with topical tretinoin: a case report. 735
Treatment of localized discoid lupus erythematosus with tazarotene. 735
Efficacy of tacrolimus 0.1% ointment in cutaneous lupus erythematosus: a multicenter, randomized, double-blind, vehicle-controlled trial. 735
Pimecrolimus 1% cream for cutaneous lupus erythematosus. 735
Second-line therapies 735
Dapsone is an effective therapy for the skin lesions of subacute cutaneous lupus erythematosus and urticarial vasculitis in a patient with C2 deficiency. 735
A case of SLE with acute, subacute and chronic cutaneous lesions successfully treated with dapsone. 735
Treatment of chronic discoid lupus erythematosus with an oral gold compound (auranofin). 735
Thalidomide in the treatment of cutaneous lupus erythematosus refractory to conventional therapy. 735
Low-dose thalidomide therapy for refractory cutaneous lesions of lupus erythematosus. 735
Long-term thalidomide use in refractory cutaneous lesions of lupus erythematosus: a series of 65 Brazilian patients. 735
Thalidomide in the treatment of refractory cutaneous lupus erythematosus: prognostic factors of clinical outcome. 735
Thalidomide in cutaneous lupus erythematosus. 735
Mechanism-oriented assessment of isotretinoin in chronic or subacute cutaneous lupus erythematosus. 736
Azathioprine: an effective, corticosteroid-sparing therapy for patients with recalcitrant cutaneous lupus erythematosus or with recalcitrant cutaneous leukocytoclastic vasculitis. 736
Mycophenolate sodium for subacute cutaneous lupus erythematosus resistant to standard therapy. 736
Efficacy of mycophenolate mofetil in antimalarial-resistant cutaneous lupus erythematosus. 736
Efficacy and safety of methotrexate in recalcitrant cutaneous lupus erythematosus: results of a retrospective study in 43 patients. 736
Pulse cyclophosphamide treatment for severe refractory cutaneous lupus erythematosus. 736
Third-line therapies 736
Clofazimine (Lamprene) in the treatment of discoid lupus erythematosus. 736
Double-blind, randomized, controlled clinical trial of clofazimine compared with chloroquine in patients with systemic lupus erythematosus. 736
Phenytoin in the treatment of discoid lupus erythematosus. 737
Intravenous immunoglobulin (IVIg) for therapy-resistant cutaneous lupus erythematosus. 737
Response of discoid and subacute cutaneous lupus erythematosus to recombinant interferon alpha-2a. 737
Treatment of severe cutaneous lupus erythematosus with a chimeric CD4 monoclonal antibody, cM-T412. 737
Regression of subacute cutaneous lupus erythematosus in a patient with rheumatoid arthritis treated with a biologic tumor necrosis factor alpha-blocking agent: comment on the article by Pisetsky and the letter from Aringer et al. 737
Case reports of etanercept in inflammatory dermatoses. 737
Successful treatment of refractory skin manifestations of systemic lupus erythematosus with rituximab: report of a case. 737
Refractory subacute cutaneous lupus erythematosus successfully treated with rituximab. 737
Successful treatment of subacute cutaneous lupus erythematosus with ustekinumab. 737
Response to Ustekinumab in a patient with both severe psoriasis and hypertrophic cutaneous lupus. 737
Ustekinumab in the treatment of refractory chronic cutaneous lupus erythematosus: a case report. 737
Leflunomide in subacute cutaneous lupus erythematosus: two sides of a coin. 737
228 Subcorneal pustular dermatosis 738
Management strategy 738
Specific investigations 738
Subcorneal pustular dermatosis: 50 years on. 738
Subcorneal pustular dermatosis: a clinical study of ten patients. 738
Subcorneal pustular dermatosis (Sneddon–Wilkinson disease) in association with a monoclonal IgA gammopathy: a report and review of the literature. 738
Subcorneal pustular dermatosis and IgA λ myeloma: an uncommon association but probably not coincidental. 738
Sneddon–Wilkinson disease in association with rheumatoid arthritis. 738
First-line therapies 739
229 Subcutaneous fat necrosis of the newborn 741
Management strategy 741
Fine-needle aspiration cytology of subcutaneous fat necrosis of the newborn: the cytology spectrum with review of the literature. 741
MRI and ultrasound findings of subcutaneous fat necrosis of the newborn. 741
Hypercalcemia and metastatic calcification in a neonate with subcutaneous fat necrosis. 741
Subcutaneous fat necrosis of the newborn: a review of 11 cases. 742
Subcutaneous fat necrosis after moderate therapeutic hypothermia in neonates. 742
Specific investigations 742
Subcutaneous fat necrosis of the newborn: be aware of hypercalcaemia. 742
First-line therapies 742
Subcutaneous fat necrosis of the newborn. 742
Second-line therapies 742
Intravenous bisphosphonate for hypercalcemia accompanying subcutaneous fat necrosis: a novel treatment approach. 742
Subcutaneous fat necrosis with hypercalcemia. 742
Third-line therapies 742
Pamidronate: treatment for severe hypercalcemia in neonatal subcutaneous fat necrosis. 742
Effectiveness of pamidronate in severe neonatal hypercalcemia caused by subcutaneous fat necrosis: a case report. 742
230 Sweet syndrome 743
Management strategy 743
Specific investigations 743
Sweet’s syndrome revisited: a review of disease concepts. 743
The relationship between neutrophilic dermatosis of the dorsal hands and Sweet syndrome: report of 9 cases and comparison to atypical pyoderma gangrenosum. 743
Histiocytoid Sweet syndrome. 743
Chronic recurrent lymphocytic Sweet syndrome as a predictive marker of myelodysplasia. 743
Necrotizing Sweet syndrome. 743
Neonatal Sweet syndrome. 743
First-line therapies 743
Sweet’s syndrome: a review of current treatment options. 743
Second-line therapies 743
Potassium iodide in dermatology: a 19th century drug for the 21st century – uses, pharmacology, adverse effects, and contraindications. 744
Long-term suppression of chronic Sweet’s syndrome with colchicine. 744
Indomethacin treatment of eighteen patients with Sweet’s syndrome. 744
Association of acute neutrophilic dermatosis and myelodysplastic syndrome with (6;9) chromosome translocation: a case report and review of the literature. 744
Sweet’s syndrome and malignancy in the UK. 744
Sweet’s syndrome in association with generalized granuloma annulare in a patient with previous breast cancer. 744
Sweet’s syndrome. 744
Sweet’s syndrome in association with Crohn’s disease: report of a case and review of the literature. 744
Third-line therapies 744
Peripheral ulcerative keratitis: an extracutaneous neutrophilic disorder. Report of a patient with rheumatoid arthritis, pustular vasculitis, pyoderma gangrenosum, and Sweet’s syndrome with an excellent response to cyclosporine therapy. 744
Systemic interferon-alpha treatment for idiopathic Sweet’s syndrome. 744
Lymphocytic infiltrates as a presenting feature of Sweet’s syndrome with myelodysplasia and response to cyclophosphamide. 744
Treatment of recurrent Sweet’s syndrome with coexisting rheumatoid arthritis with the tumor necrosis factor antagonist etanercept. 744
Thalidomide in the treatment of recalcitrant Sweet’s syndrome associated with myelodysplasia. 744
The use of pulse methylprednisolone and chlorambucil in the treatment of Sweet’s syndrome. 745
Efficacy of anti-interleukin-1 receptor antagonist anakinra (Kineret) in a case of refractory Sweet’s syndrome. 745
Pediatric Sweet syndrome and immunodeficiency successfully treated with intravenous immunoglobulin. 745
231 Syphilis 746
Management Strategy 746
Incubation period 746
Primary syphilis 746
Secondary syphilis 747
Neurological syphilis 747
Latent syphilis 747
Tertiary syphilis 747
Diagnostics and treatment 747
Specific investigations 748
232 Syringomata 750
Management strategy 750
Specific investigations 750
First-line therapies 750
Cosmetic dermatologic surgery, 2nd edn. 750
An easy method for removal of syringoma. 750
True electrocautery in the treatment of syringomas and other benign cutaneous lesions. 750
Intralesional electrodesiccation of syringomas. 750
Syringomas treated by intralesional insulated needles without epidermal damage. 750
Treatment of multiple facial syringomas with the carbon dioxide (CO2) laser. 751
Treatment of syringoma using an ablative 10,600-nm carbon dioxide fractional laser. 751
Periorbital syringoma treated with radiofrequency and carbon dioxide (CO2) laser in five patients. 751
Second-line therapies 751
Syringoma: removal by electrodesiccation and curettage. 751
Cryosurgery. 751
A new treatment for syringoma. Combination of carbon dioxide laser and trichloroacetic acid. 751
Third-line therapies 751
Dermabrasion by diamond fraises revolving at 85000 revolutions per minute. 751
The treatment of eruptive syringomas in an African American patient with a combination of trichloroacetic acid and CO2 laser destruction. 751
Eruptive pruritic syringomas: treatment with topical atropine. 751
Eruptive syringoma: treatment with topical tretinoin. 751
233 Tinea capitis 752
Management strategy 752
Specific investigations 753
Fungal Infection: Diagnosis and Management. 753
Screening for asymptomatic carriage of Trichophyton tonsurans in household contacts of patients with tinea capitis: results of 209 patients from south London. 753
Tinea capitis: predictive value of symptoms and time to cure with griseofulvin treatment. 753
First-line therapies 753
Meta-analysis of randomized controlled studies comparing griseofulvin and terbinafine in the treatment of tinea capitis. 753
Terbinafine hydrochloride oral granules versus oral griseofulvin suspension in children with tinea capitis: results of two randomised investigator-blinded, multicenter, international, controlled trials. 753
Systemic anti-fungal therapy for tinea capitis in children. 753
Itraconazole in the treatment of tinea capitis caused by Microsporum canis: experience in a large cohort. 753
Tinea capitis in early infancy treated with itraconazole. 754
Second-line therapies 754
Comparative evaluation of griseofulvin, terbinafine and fluconazole in the treatment of tinea capitis. 754
Therapeutic options for the treatment of tinea capitis caused by Trichophyton species: griseofulvin versus the new oral antifungal agents, terbinafine, itraconazole and fluconazole. 754
Once weekly fluconazole is effective in children in the treatment of tinea capitis: a prospective multi-centre study. 754
Short duration treatment with terbinafine for tinea capitis caused by Trichophyton or Microsporum species. 754
Third-line therapies 754
A retrospective study of the management of pediatric kerion in T. tonsurans infection. 754
A randomised comparative trial of treatment of kerion celsi with griseofulvin plus oral prednisolone vs. griseofulvin alone. 754
Successful treatment of tinea capitis with 2% ketoconazole shampoo. 755
Comparison of 1% and 2.5% selenium sulphide in the treatment of tinea capitis. 755
Prophylactic ketoconazole shampoo for tinea capitis in a high risk pediatric population. 755
234 Tinea pedis and skin dermatophytosis 756
Epidemiology of dermatophytoses: retrospective analysis from 2005 to 2010 and comparison with previous data from 1975. 756
Management strategy 756
Chronic dermatomycoses of the foot as risk factors for acute bacterial cellulitis of the leg: a case-control study. 756
Specific investigations 756
Clinical signs and procedures in dermatology. 756
Epidemiological trends in skin mycoses worldwide. 756
Frequency of culture-proven dermatophyte infection in patients with suspected tinea pedis. 757
Interdigital athlete’s foot. The interaction of dermatophytes and resident bacteria. 757
Inflammatory tinea pedis/manuum masquerading as bacterial cellulitis. 757
First-line therapies 757
Systematic review of topical treatments for fungal infections of the skin and nails of the feet. 757
Efficacy of topical antifungal drugs in different dermatomycoses: a systematic review with meta-analysis. 757
Sertaconazole: a review of its use in the management of superficial mycoses in dermatology and gynaecology. 757
Second-line therapies 757
Comparable efficacy and safety of various topical formulations of terbinafine in tinea pedis irrespective of the treatment regimen: results of a meta-analysis. 757
Ciclopirox gel in the treatment of patients with interdigital tinea pedis. 757
Ciclopirox: recent nonclinical and clinical data relevant to its use as a topical antimycotic agent. 757
Third-line therapies 757
The use of 40% urea cream in the treatment of moccasin tinea pedis. 757
Photodynamic therapy in the treatment of superficial mycoses: an evidence-based evaluation. 758
Short-term itraconazole versus terbinafine in the treatment of tinea pedis or manus. 758
A multicentre (double-blind) comparative study to assess the safety and efficacy of fluconazole and griseofulvin in the treatment of tinea corporis and tinea cruris. 758
Efficacy and safety of short-term itraconazole in tinea pedis: a double-blind, randomized, placebo-controlled trial. 758
Therapy with fluconazole for tinea corporis, tinea cruris, and tinea pedis. 758
Safety and efficacy of short-duration oral terbinafine for the treatment of tinea corporis or tinea cruris in subjects with HIV infection or diabetes. 758
235 Tinea unguium 759
Factors influencing coexistence of toenail onychomycosis with tinea pedis and other dermatomycoses: a survey of 2761 patients. 759
Management Strategy 759
Specific investigations 760
Cost-effectiveness of diagnostic tests for toenail onychomycosis: a repeated-measure, single-blinded, cross-sectional evaluation of 7 diagnostic tests. 760
Fast and sensitive detection of Trichophyton rubrum DNA from the nail samples of patients with onychomycosis by a double-round polymerase chain reaction-based assay. 760
A new classification system for grading the severity of onychomycosis: Onychomycosis Severity Index. 760
First-line therapies – SYSTEMIC 760
Onychomycosis: diagnosis and definition of cure. 760
Cumulative meta-analysis of systemic antifungal agents for the treatment of onychomycosis. 760
The successful treatment of Trichophyton rubrum nail bed (distal subungual) onychomycosis with intermittent pulse-dosed terbinafine. 760
Second-line therapies 760
Itraconazole for the treatment of onychomycosis. 761
A double-blind, randomized study to compare the efficacy and safety of terbinafine (Lamisil) with fluconazole (Diflucan) in the treatment of onychomycosis. 761
The safety of oral antifungal treatments for superficial dermatophytosis and onychomycosis: a meta-analysis. 761
A randomized, placebo- and active-controlled, parallel-group, multicentre, investigator-blinded study of four treatment regimens of posaconazole in adults with toenail onychomycosis. 761
Third-line therapies 761
A multicentre, randomized, controlled study of the efficacy, safety and cost-effectiveness of a combination therapy with amorolfine nail lacquer and oral terbinafine compared with oral terbinafine alone for the treatment of onychomycosis with matrix involvement. 761
Treatment of toenail onychomycosis with oral terbinafine plus aggressive debridement: IRON-CLAD, a large, randomized, open-label, multicenter trial. 761
New therapeutic options for onychomycosis. 761
TOPICAL THERAPIES 761
A multicentre, randomized, controlled study of the efficacy, safety and cost-effectiveness of a combination therapy with amorolfine nail lacquer and oral terbinafine compared with oral terbinafine alone for the treatment of onychomycosis with matrix involvement. 761
Ciclopirox nail lacquer topical solution 8% in the treatment of toenail onychomycosis. 762
Efficacy, safety and tolerability of topical terbinafine nail solution in patients with mild-to-moderate toenail onychomycosis: results from three randomized studies using double-blind vehicle-controlled and open-label active- controlled designs. 762
236 Tinea versicolor (pityriasis versicolor) 763
Management Strategy 763
Specific investigations 763
First-line therapy 763
Pityriasis versicolor: a review of pharmacological treatment options. 763
Flutrimazole shampoo 1% versus ketoconazole shampoo 2% in the treatment of pityriasis versicolor. A randomized double-blind comparative trial. 764
Second-line therapy 764
Fluconazole vs. itraconazole in the treatment of tinea versicolor. 764
Comparison of a single 400 mg dose versus a 7-day 200 mg daily dose of itraconazole in the treatment of tinea versicolor. 764
Fluconazole versus ketoconazole in the treatment of tinea versicolor. 764
Efficacy of itraconazole in the prophylactic treatment of pityriasis (tinea) versicolor. 764
Single-dose fluconazole versus itraconazole in pityriasis versicolor. 764
Comparison between fluconazole and ketoconazole effectivity in the treatment of pityriasis versicolor. 764
Single-dose oral fluconazole versus topical clotrimazole in patients with pityriasis versicolor: a double-blind randomized controlled trial. 764
Third-line therapy 764
A double-blind, randomized, placebo-controlled, dose-finding study of oral pramiconazole in the treatment of pityriasis versicolor. 764
Roles of adapalene in the treatment of pityriasis versicolor. 765
An open-label study of naftifine hydrochloride 1% gel in the treatment of tinea versicolor. 765
Tinea versicolor clearance with oral isotretinoin therapy. 765
237 Toxic epidermal necrolysis and Stevens–Johnson syndrome 766
Management Strategy 766
Specific investigations 767
Pulmonary complications in toxic epidermal necrolysis: a prospective clinical study. 767
Incidence of Stevens–Johnson syndrome and toxic epidermal necrolysis in patients with the acquired immunodeficiency syndrome in Germany. 767
Stevens–Johnson syndrome and toxic epidermal necrolysis: assessment of medication risks with emphasis on recently marketed drugs. The EuroSCAR study. 767
SCORTEN: a severity-of-illness score for toxic epidermal necrolysis. 767
First-line therapies 767
Toxic epidermal necrolysis: current evidence, practical management and future directions. 767
Toxic epidermal necrolysis and Stevens–Johnson syndrome: does early withdrawal of causative drugs decrease the risk of death? 767
ALDEN, an algorithm for assessment of drug causality in Stevens–Johnson syndrome and toxic epidermal necrolysis: comparison with case-control analysis. 767
A multicenter review of toxic epidermal necrolysis treated in U.S. burn centers at the end of the twentieth century. 767
Toxic epidermal necrolysis: use of Biobrane for skin coverage reduces pain, improves mobilization and decreases infection in elderly patients. 767
Second-line therapies 768
Open trial of cyclosporine treatment for Stevens–Johnson syndrome and toxic epidermal necrolysis. 768
Treatment of toxic epidermal necrolysis with cyclosporine A. 768
Improved burn center survival of patients with toxic epidermal necrolysis managed without corticosteroids. 768
Erythema multiforme in children. Response to treatment with systemic corticosteroids. 768
Characteristics of toxic epidermal necrolysis in patients undergoing long-term glucocorticoid therapy. 768
High-dose systemic corticosteroids can arrest recurrences of severe mucocutaneous erythema multiforme. 768
Corticosteroid therapy in an additional 13 cases of Stevens–Johnson syndrome: a total series of 67 cases. 768
Effects of treatments on the mortality of Stevens–Johnson syndrome and toxic epidermal necrolysis: a retrospective study on patients included in the prospective EuroSCAR study. 768
Inhibition of toxic epidermal necrolysis by blockade of CD95 with human intravenous immunoglobulin. 768
Intravenous immunoglobulin treatment for Stevens–Johnson syndrome and toxic epidermal necrolysis: a prospective noncomparative study showing no benefit on mortality or progression. 768
Treatment of toxic epidermal necrolysis with high-dose intravenous immunoglobulins: multicenter retrospective analysis of 48 consecutive cases. 768
Intravenous immunoglobulin does not improve outcome in toxic epidermal necrolysis. 769
Third-line therapies 769
Plasmapheresis as an adjunct treatment in toxic epidermal necrolysis. 769
Lack of significant treatment effect of plasma exchange in the treatment of drug-induced toxic epidermal necrolysis? 769
Plasma exchange in patients with toxic epidermal necrolysis. 769
Pentoxifylline in toxic epidermal necrolysis and Stevens–Johnson syndrome. 769
Randomised comparison of thalidomide versus placebo in toxic epidermal necrolysis. 769
238 Transient acantholytic dermatosis (Grover disease) 770
Management strategy 770
Specific investigations 770
First-line therapies 770
Transient acantholytic dermatosis. 770
Incidence of transient acantholytic dermatosis (Grover’s disease) in a hospital setting. 770
Transient acantholytic dermatosis (Grover disease). 770
Second-line therapies 770
Persistent acantholytic dermatosis. 770
Grover’s disease treated with isotretinoin. 771
Transient acantholytic dermatosis treated with isotretinoin. 771
Response of transient acantholytic dermatosis to photochemotherapy. 771
Photochemotherapy beyond psoriasis. 771
Treatment of transient acantholytic dermatosis. 771
Third-line therapies 771
Treatment of Grover’s disease with calcipotriol (Dovonex). 771
Successful treatment of Grover’s disease with calcipotriol. 771
Treatment of Grover’s disease with tacalcitol. 771
Effective treatment of persistent Grover’s disease with tricholoroacetic acid peeling. 771
Medium-dose ultraviolet A1 phototherapy in transient acantholytic dermatosis (Grover’s disease). 771
Remission of transient acantholytic dermatosis after the treatment with rituximab for follicular lymphoma. 771
Use of etanercept in treating pruritus and preventing new lesions in Grover disease. 772
239 Trichotillomania 773
Management strategy 773
Specific investigations 774
Trichotillomania: a histopathological study in 66 patients. 774
Diagnosis and management of trichotillomania in children and adolescents. 774
Gastrointestinal bezoars: sonographic and CT characteristics. 774
Laparoscopic removal of huge gastric trichobezoar. 774
First-line therapies 774
Trichotillomania and related disorders in children and adolescents. 774
Trichotillomania treatment. 774
Use of psychotropic drugs in dermatology. 774
Second-line therapies 774
Treatment of trichotillomania with behavioural therapy or fluoxetine: a randomized waiting list study. 774
Behavioural treatment of trichotillomania: two-year follow-up results. 774
Single modality versus dual modality treatment for trichotillomania. 774
240 Tuberculosis and tuberculids 775
Management strategy 775
Specific investigations 775
Usefulness of interferon-γ release assays in the diagnosis of erythema induratum. 775
Comparison of QuantiFERON-TB Gold test and tuberculin skin test for the identification of latent Mycobacterium tuberculosis infection in lupus patients. 775
PCR based detection of mycobacteria in paraffin wax embedded material routinely processed for morphological examination. 775
Papulonecrotic tuberculid. Identification of Mycobacterium tuberculosis DNA by polymerase chain reaction. 776
First-line therapies 776
Treatment of Tuberculosis: Guidelines for National Programmes, 4th ed. 776
Clinical diagnosis and management of tuberculosis, and measures for its prevention and control. 776
Comparative efficacy of drug regimens in skin tuberculosis. 776
Atypical cutaneous tuberculosis in a patient with rheumatoid arthritis treated with infliximab. 776
An unusual case of vulval papulonecrotic tuberculid. 776
Plaques on a butcher’s fingers. 776
Second-line therapies 776
Scrofuloderma of the lower extremity treated with wide resection: a case report and review of the literature. 776
Lupus vulgaris of the ear lobe. 776
Lupus vulgaris responding to calcipotriol. 776
Vitamin D in treatment of cutaneous tuberculosis. 776
241 Urticaria and angioedema 777
Management strategy 777
Specific investigations 777
Guidelines for evaluation and management of urticaria in adults and children. 778
The effectiveness of a history-based diagnostic approach in chronic urticaria and angioedema. 778
Syndrome of idiopathic chronic urticaria and angioedema with thyroid autoimmunity: a study of 90 patients. 778
Chronic urticaria and associated coeliac disease in children: a case control study. 778
First-line therapies 778
Chronic urticaria: assessment of current treatment. 778
The effectiveness of levocetirizine and desloratadine in up to 4 times conventional doses in difficult-to-treat urticaria. 778
Second-line therapies 778
Desloratidine in combination with montelukast in the treatment of chronic urticaria: a randomized, double-blind, placebo-controlled study. 778
Effects of pseudoallergen-free diet on chronic spontaneous urticaria: a prospective trial. 778
Outpatient management of acute urticaria: the role of prednisone. 778
Histamine H2-receptor antagonists for urticaria. 778
Effectiveness of Helicobacter pylori eradication in chronic urticaria: evidence-based analysis using the Grading of Recommendations Assessment, Development, and Evaluation system. 778
Double-blind crossover study comparing doxepin with diphenhydramine for the treatment of chronic urticaria. 778
Therapy of chronic idiopathic urticaria with nifedipine: demonstration of beneficial effect in a double-blinded, placebo-controlled, crossover trial. 779
Treatment of chronic urticaria with PUVA or UVA plus placebo: a double-blind study. 779
Treatment of chronic urticaria with narrowband ultraviolet B phototherapy: a randomized controlled trial. 779
Successful treatment of recalcitrant urticaria with sulfasalazine. 779
Warfarin treatment of chronic idiopathic urticaria and angio-oedema. 779
Stanozolol in chronic urticaria: a double blind, placebo controlled trial. 779
Non-hereditary angioedema treated with tranexamic acid. 779
Efficacy and safety of desloratidine combined with dipyridamole in the treatment of chronic urticaria. 779
Improvement of chronic idiopathic urticaria with L- thyroxine: a new TSH role in immune response? 779
Treatment of chronic idiopathic urticaria with levamisole: a multicentre, randomized, double-blind, controlled trial. 779
Third-line therapies 779
Cyclosporine in chronic idiopathic urticaria: a double blind, randomized, placebo-controlled trial. 779
Evidence for methotrexate as a useful treatment for steroid-dependent chronic urticaria. 779
Plasmapheresis for severe, unremitting, chronic urticaria. 779
Intravenous immunoglobulin in autoimmune chronic urticaria. 779
Treatment of severe chronic idiopathic urticaria with oral mycophenolate mofetil in patients not responding to antihistamines and/or corticosteroids. 779
Tacrolimus in the treatment of severe chronic idiopathic urticaria: an open-label prospective study. 780
A randomized, placebo-controlled, dose-ranging study of single-dose omalizumab in patients with H1-antihistamine-refractory chronic idiopathic urticaria. 780
242 Varicella 781
Management strategy 781
Specific investigations 782
The diagnosis of viral infections. 782
First-line therapies 782
Acyclovir for treating varicella in otherwise healthy children and adolescents. 782
The use of oral acyclovir in otherwise healthy children with varicella. 782
Acyclovir treatment of varicella in otherwise healthy adolescents. 782
Treatment of adult varicella with oral acyclovir: A randomized, placebo-controlled trial. 782
Second-line therapies 782
Foscarnet therapy in five patients with AIDS and acyclovir resistant varicella zoster virus infection. 782
Varicella in a pediatric heart transplant population on nonsteroid maintenance immunosuppression. 782
Pregnancy 782
Chickenpox in pregnancy. 782
Management of varicella infection (chickenpox) in pregnancy. 782
Prophylaxis 783
Prevention of varicella. Recommendations of the Advisory Committee on Immunization Practices (ACIP). 783
Oka/Merck varicella vaccine in healthy children: final report of a 2-year efficacy study and 7-year follow-up studies. 783
Safety and immunogenicity of a combination measles, mumps, rubella and varicella vaccine (ProQuad). 783
Association between vaccination for herpes zoster and risk of herpes zoster infection among older patients with selected immune-mediated diseases. 783
A varicella outbreak in a school with high one-dose vaccination coverage, Beijing, China. 783
Evaluation of varicella zoster immune globulin: protection of immunosuppressed children after household exposure to varicella. 783
Intravenous immunoglobulin prophylaxis in children with acute leukaemia following exposure to varicella. 783
Postexposure prophylaxis of varicella in family contact by oral acyclovir. 783
Antiviral prophylaxis and treatment in chickenpox. A review prepared for the UK Advisory Group on Chickenpox on behalf of the British Society for the Study of Infection. 783
243 Viral exanthems: 784
Rubella 784
Management Strategy 784
Specific investigations 784
Confirmation of rubella within 4 days of rash onset: comparison of rubella virus RNA detection in oral fluid with immunoglobulin M detection in serum or oral fluid. 784
A protein microarray immunoassay for the serological evaluation of the antibody response in vertically transmitted infections. 784
First-line therapies 784
The epidemiological profile of rubella and congenital rubella syndrome in the United States, 1998–2004: the evidence for absence of endemic transmission. 784
Observational safety study of febrile convulsion following first dose MMRV vaccination in a managed care setting. 785
Roseola 785
244 Viral warts 788
Management strategy 788
First–line therapies 788
An assessment of methods of treating viral warts by comparative treatment trials based on a standard design. 788
Cryotherapy versus salicylic acid for the treatment of plantar warts: a randomised controlled trial. 788
Local treatment for cutaneous warts. 788
Efficacy of silver nitrate pencils in the treatment of common warts. 789
Efficacy of 10% silver nitrate solution in the treatment of common warts: a placebo-controlled, randomized, clinical trial. 789
Cryosurgical treatment of warts: dimethyl ether and propane versus liquid nitrogen: case report and review of the literature. 789
Second-line therapy 789
A two-week interval is better than a three-week interval for reducing the recurrence rate of hand–foot viral warts after cryotherapy: a retrospective review of 560 hand–foot viral warts patients. 789
Liquid nitrogen cryotherapy of common warts: cryo-spray versus cotton wool bud. 789
Cryotherapy of common viral warts at intervals of 1, 2 and 3 weeks. 789
Value of a second freeze–thaw cycle in cryotherapy of common warts. 789
Third-line therapy 789
Local 789
Bleomycin in the treatment of recalcitrant warts. 789
Dermojet delivery of bleomycin for the treatment of recalcitrant plantar warts. 790
Intralesional bleomycin in the treatment of cutaneous warts: a randomized clinical trial comparing it with cryotherapy. 790
Photodynamic therapy using light-emitting diodes for the treatment of viral warts. 790
Efficacy of topical aminolaevulinic acid photodynamic therapy for the treatment of verruca planae. 790
Photodynamic therapy with 5-aminolaevulinic acid or placebo for recalcitrant foot and hand warts: randomised double-blind trial. 790
The efficacy of duct tape vs. cryotherapy in the treatment of verruca vulgaris (the common wart). 790
Efficacy of duct tape vs placebo in the treatment of verruca vulgaris (warts) in primary school children. 790
Duct tape for the treatment of common warts in adults: a double blind randomized controlled trial. 790
A controlled trial on the use of topical 5-fluorouracil on viral warts. 790
Topical 5% 5-fluorouracil cream in the treatment of plantar warts: a prospective randomised and controlled clinical study. 790
Topical zinc oxide vs. salicylic acid-lactic acid combination in the treatment of warts. 790
Treatment of viral warts by intralesional injection of zinc sulphate. 790
Treatment of skin papillomas with topical α-lactalbumin–oleic acid. 790
Recalcitrant viral warts treated by diphencyprone immunotherapy. 790
The use of DCP in the treatment of recalcitrant warts. 790
Does immunotherapy of viral warts provide beneficial effects when it is combined with conventional therapy? 790
Comparative study on the sustained efficacy of diphencyprone immunotherapy versus cryotherapy in viral warts. 790
Squaric acid immunotherapy for warts in children. 791
Autowart injection therapy for recalcitrant warts. 791
Immunotherapy for recalcitrant warts in children using intralesional mumps or candida antigens. 791
Intralesional immunotherapy for warts using a combination of skin test antigens: a safe and effective therapy. 791
Topical treatment of warts and mollusca with imiquimod. 791
Topical 5% imiquimod long-term treatment of cutaneous warts resistant to standard therapy modalities. 791
Pulsed dye laser treatment for viral warts: a study of 120 patients. 791
Pulsed dye laser treatment is effective in the treatment of recalcitrant viral warts. 791
Treatment of recalcitrant viral warts with pulsed dye laser MAL-PDT. 791
Comparative study of aminolevulinic acid photodynamic therapy plus pulsed dye laser versus pulsed dye laser alone in treatment of viral warts. 791
Combination of carbon dioxide laser therapy and artificial dermis application in plantar warts: human papilloma virus DNA analysis after treatment. 791
Successful treatment of recalcitrant warts in paediatric patients with carbon dioxide laser. 791
Er : YAG laser followed by topical podophyllotoxin for hard to treat palmoplantar warts. 791
Local hyperthermia at 44°C for the treatment of plantar warts: a randomized, patient-blinded, placebo-controlled trial. 791
Controlled localized heat therapy in cutaneous warts. 791
Nd : YAG laser hyperthermia in the treatment of recalcitrant verrucae vulgares (Regensburg’s technique). 792
A double blind, randomized trial of local formic acid puncture technique in the treatment of common warts. 792
Topical formic acid puncture technique for the treatment of common warts. 792
Glycolic acid 15% plus salicylic acid 2%: a new therapeutic pearl for facial flat warts. 792
Evaluation of topical potassium hydroxide solution for treatment of plane warts. 792
Comparative study of fig tree efficacy in the treatment of common warts vs. cryotherapy. 792
Treatment of plantar verruca using 2% sodium salicylate iontophoresis. 792
Topical treatment of resistant warts with glutaraldehyde. 792
Cutaneous necrosis secondary to topical treatment of wart with 20 p. 100 glutaraldehyde solution. 792
Treatment of plantar warts in children. 792
Plantar warts treated with topical adapalene. 792
Treatment of verruca with alpha-2 interferon. 792
Long-term follow-up evaluation of patients with electro-surgically treated warts. 792
The treatment of viral warts with topical cidofovir 1%: our experience of seven paediatric patients. 792
Large plantar wart caused by HPV-66 and resolution by topical cidofovir therapy. 792
Systemic 792
Cimetidine therapy for warts: a placebo-controlled, double-blind study. 792
Cimetidine therapy for recalcitrant warts in adults: is it any better than placebo? 792
Cimetidine therapy for recalcitrant warts in adults. 793
Comparison of combination of cimetidine and levamisole with cimetidine alone in the treatment of recalcitrant warts. 793
Verrucae treated by levamisole. 793
Levamisole in a double-blind study: no effect on warts. 793
Oral supplementation with a nutraceutical containing echinacea, methionine and antioxidant/immunostimulating compounds in patients with cutaneous viral warts. 793
Oral zinc sulphate treatment for viral warts: an open-label study. 793
Oral zinc sulphate in the treatment of recalcitrant viral warts: randomized placebo controlled clinical trial. 793
Smoke from leaves of Populus euphratica Olivier vs. conventional cryotherapy for the treatment of cutaneous warts: a pilot, randomized, single blind, prospective study. 793
Treatment of extensive warts with etretinate: a clinical trial of 20 children. 793
Use of acitretin in the treatment of resistant viral warts. 793
Acitretin in management of diffuse common warts: a case report. 793
Effects of hypnotic, placebo, and salicylic acid treatments on wart regression. 793
245 Vitiligo 794
Management strategy 794
Specific investigations 795
Clinical and immunological studies in vitiligo in the United Arab Emirates. 795
Autoimmune diseases in vitiligo: do anti-nuclear antibodies (ANA) decrease thyroid volume? 795
Histopathologic features in vitiligo. 795
New insights into the pathogenesis of vitiligo: imbalance of epidermal cytokines at sites of lesions. 795
First-line therapies 795
Effectiveness of 0.1% topical tacrolimus in adult and children patients with vitiligo. 795
A double-blind randomized trial of 0.1% tacrolimus vs 0.05% clobetasol for the treatment of childhood vitiligo. 795
Effect of PUVA therapy on melanocytes and keratinocytes in non-segmental vitiligo: histopathological, immuno- histochemical and ultrastructural study. 795
Randomized double-blind trial of treatment of vitiligo: efficacy of psoralen-UV-A therapy vs narrowband-UV-B therapy. 796
Narrow-band UVB for the treatment of generalized vitiligo in children. 796
Response of vitiligo to narrowband ultraviolet B and oral antioxidants. 796
Response to narrow-band UVB – vitiligo-melasma versus vitiligo: a comparative study. 796
The effect of 308nm excimer laser on segmental vitiligo: a retrospective study of 80 patients with segmental vitiligo. 796
Treatment of vitiligo using the 308-nm excimer laser. 796
Tacrolimus ointment promotes repigmentation of vitiligo in children: a review of 57 cases. 796
Combined excimer laser and topical tacrolimus for the treatment of vitiligo: a pilot study. 796
Randomized controlled trial comparing the effectiveness of 308-nm excimer laser alone or in combination with topical hydrocortisone 17-butyrate cream in the treatment of vitiligo of the face and neck. 796
Treatment of vitiligo with narrowband-UVB (TL01) combined with tacrolimus ointment (0.1%) vs. placebo ointment, a randomized right/left double-blind comparative study. 796
The efficacy of pimecrolimus 1% cream plus narrow-band ultraviolet B in the treatment of vitiligo: a double-blind, placebo-controlled clinical trial. 796
The efficacy of pimecrolimus 1% cream combined with microdermabrasion in the treatment of nonsegmental childhood vitiligo: a randomized placebo-controlled study. 796
Combination of narrow band UVB and topical calcipotriol for the treatment of vitiligo. 796
Comparison between 308-nm monochromatic excimer light and narrowband UVB phototherapy (311–313 nm) in the treatment of vitiligo – a multicentre controlled study. 797
Vitiligo treatment with monochromatic excimer light (MEL) and tacrolimus: results of an open randomized controlled study. 797
Narrow-band UV-B micro-phototherapy: a new treatment for vitiligo. 797
Second-line therapies 797
Treatment of vitiligo with oral 5-methoxypsoralen. 797
Third-line therapies 797
Monobenzyl ether of hydroquinone. 797
Comparative evaluation of the therapeutic efficacy of dermabrasion, dermabrasion combined with topical 5% 5-fluorouracil cream, and dermabrasion combined with topical placentrex gel in localized stable vitiligo. 797
A systematic review of autologous transplantation methods in vitiligo. 797
Autologous melanocyte transfer via epidermal grafts for lip vitiligo. 797
Treatment of vitiligo by transplantation of cultured pure melanocyte suspension: analysis of 120 cases. 797
Repigmentation of vitiligo with punch grafting and narrow-band UV-B (311 nm) – a prospective study. 797
Comparison of minipunch grafting versus split-skin grafting in chronic stable vitiligo. 797
Autologous noncultured melanocyte transplantation for stable vitiligo: can suspending autologous melanocytes in the patients’ own serum improve repigmentation and patient satisfaction? 797
Subjective and objective evaluation of noncultured epidermal cellular grafting for repigmenting vitiligo. 798
Single hair grafting for the treatment for vitiligo. 798
Depigmentation therapy in vitiligo universalis with topical 4-methoxyphenol and the Q-switched ruby laser. 798
Combination treatment by 10 600 nm ablative fractional carbon dioxide laser and narrowband ultraviolet B in refractory nonsegmental vitiligo (NSV): a prospective, randomized half-body comparative study. 798
Evaluation of cosmetic tattooing in localized stable vitiligo. 798
246 Vulvodynia 799
Management Strategy 799
Specific investigations 799
Approach to the patient with vulvovaginal complaints. 799
Vulvodynia interventions – systematic review and evidence grading. 799
Guidelines for the management of vulvodynia. 799
Approach to the diagnosis and treatment of vulvar pain. 799
The vulvodynia guideline. 799
First-line therapies 799
Oral desipramine and topical lidocaine for vulvodynia: a randomized controlled trial. 799
Treatment of vulvodynia with tricyclic antidepressants: efficacy and associated factors. 800
Response to treatment in dysaesthetic vulvodynia. 800
Overnight 5% lidocaine ointment for treatment of vulvar vestibulitis. 800
Evaluation of gabapentin in the treatment of generalized vulvodynia, unprovoked. 800
Pregabalin-induced remission in a 62-year-old woman with a 20-year history of vulvodynia. 800
Topical gabapentin in the treatment of localized and generalized vulvodynia. 800
Pelvic floor muscle assessment outcomes in women with and without provoked vestibulodynia and the impact of a physical therapy program. 800
Does physiotherapy treatment improve the self-reported pain levels and quality of life in women with vulvodynia? A pilot study. 800
Second-line therapies 800
Treating vulvar vestibulitis with electromyographic biofeedback of pelvic floor musculature. 800
EMG biofeedback versus topical lidocaine gel: a randomized study for the treatment of women with vulvar vestibulitis. 800
Safety and efficacy of topical nitroglycerin for treatment of vulvar pain in women with vulvodynia: a pilot study. 800
Acupuncture for the treatment of vulvar vestibulitis: a pilot study. 800
Third-line therapies 800
Efficacy of high doses of botulinum toxin A for treating provoked vestibulodynia. 801
Botulinum toxin type A: a novel treatment for provoked vestibulodynia? Results from a randomized, placebo controlled, double blinded study. 801
Topical nifedipine for the treatment of localized provoked vulvodynia. 801
Enoxaparin treatment for vulvodynia: a randomized controlled trial. 801
Influence of dietary oxalates on the risk of adult-onset vulvodynia. 801
Pudendal canal syndrome as a cause of vulvodynia and its treatment by pudendal nerve decompression. 801
A randomized comparison of group cognitive-behavioral therapy, surface electromyographic biofeedback, and vestibulectomy in the treatment of dyspareunia resulting from vulvar vestibulitis. 801
Vestibulectomy for vulvar vestibulitis. 801
Effectiveness of hypnosis for the treatment of vulvar vestibulitis syndrome: a preliminary investigation. 801
Spinal cord stimulation for the treatment of a woman with vulvovaginal burning and deep pelvic pain. 801
247 Wells syndrome 802
Management strategy 802
Specific investigations 802
Wells syndrome: a clinical and histopathologic review of seven cases. 802
Two cases of bullous eosinophilic cellulitis. 802
Wells syndrome (eosinophilic cellulitis) secondary to infliximab. 802
Eosinophilic cellulitis-like reaction to subcutaneous etanercept injection. 802
Eosinophilic annular erythema is a peculiar subtype in the spectrum of Wells syndrome: a multicentre long-term follow-up study. 802
Eosinophilic cellulitis (Wells syndrome) as a cutaneous reaction to the administration of adalimumab. 802
Wells Syndrome with multiorgan involvement mimicking hypereosinophilic syndrome. 802
Exaggerated insect bite reaction exacerbated by a pyogenic infection in a patient with chronic lymphocytic leukaemia. 802
Eosinophilic cellulitis after honeybee sting. 803
Eosinophilic cellulitis (Wells syndrome) and an insect bite-like reaction in a patient with non-Hodgkin B cell lymphoma. 803
Recurrent Wells syndrome associated with allergic asthma exacerbation. 803
Systemic lupus erythematosus associated with Wells syndrome. 803
Diffuse polymorphic eosinophilic cellulitis in a patient with metallic alloy implants: a possible association? 803
Wells syndrome associated with parvovirus in a 5-year old boy. 803
Wells syndrome associated with Churg–Strauss syndrome. 803
Eosinophilic cellulitis as a presenting feature of chronic eosinophilic leukaemia, secondary to a deletion on chromosome 4q12 creating the FIP1L1-PDGFRA fusion gene. 803
First-line treatment 803
Recurrent granulomatous dermatitis with eosinophilia. 803
Eosinophilic cellulitis. 803
Second-line treatment 803
Eosinophilic cellulitis in a child successfully treated with cetirizine. 803
Eosinophilic cellulitis (Wells syndrome) successfully treated with low-dose cyclosporine. 803
Eosinophilic cellulitis case report: treatment options. 803
Interferon alfa treatment of a patient with eosinophilic cellulitis and HIV infection. 803
Eosinophilic cellulitis (Wells syndrome): treatment with minocycline. 803
Bullous eosinophilic cellulitis associated with ulcerative colitis: effective treatment with sulfasalazine and glucocorticoids. 803
Idiopathic bullous eosinophilic cellulitis (Wells syndrome) responsive to topical tacrolimus and antihistamine combination. 803
Oral tacrolimus treatment for refractory eosinophilic cellulitis. 803
Eosinophilic cellulitis: a case study and management with griseofulvin. 803
248 Xanthomas 804
Management strategy 804
Specific investigations 804
Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis. 804
Xanthelasma palpebrarum: a marker of premature atherosclerosis (risk of atherosclerosis in xanthelasma). 804
Xanthelasmata, arcus corneae, and ischaemic vascular disease and death in general population: prospective cohort study. 804
Sitosterolaemia and xanthomatosis in a child. 805
Pathogenesis and treatment of xanthomatosis associated with monoclonal gammopathy. 805
Verruciform xanthoma: localized lymphedema (elephantiasis) is an essential pathogenic factor. 805
First-line therapies 805
Opposite effects on serum cholesteryl ester transfer protein levels between long-term treatments with pravastatin and probucol in patients with primary hypercholesterolemia. 805
A comparative study of the therapeutic effect of probucol and pravastatin on xanthelasma. 805
Effects of probucol on xanthomata regression in familial hypercholesterolemia. 805
Second-line therapies 805
Treatment of xanthelasma by excision with secondary intention healing. 805
Xanthelasma palpebrarum. 805
Upper and lower eyelid reconstruction for severe disfiguring necrobiotic xanthogranuloma. 805
Xanthelasma palpebrarum: treatment with the ultrapulsed CO2 laser. 805
Xanthelasma palpebrarum: treatment with the erbium : YAG laser. 805
Treatment of diffuse plane xanthoma of the face with erbium : YAG laser. 805
New operative technique for treatment of xanthelasma palpebrarum: laser-inverted resurfacing. Preliminary report. 805
Treatment of xanthelasma palpebrarum by 1064-nm Q-switched Nd : YAG laser: a study of 11 cases. 805
Is Q-switched neodymium-doped yttrium aluminium garnet laser an effective approach to treat xanthelasma palpebrarum? Results from a clinical study of 76 cases. 806
Treatment of xanthelasma palpebrarum with argon laser photocoagulation. 806
Histopathological study of xanthelasma palpebrarum after pulsed dye laser. 806
KTP laser coagulation for xanthelasma palpebrarum. 806
Xanthelasma palpebrarum treatment with a 1,450-nm-diode laser. 806
Effectiveness of low-voltage radiofrequency in the treatment of xanthelasma palpebrarum: a pilot study of 15 cases. 806
Third-line therapies 806
Treatment of xanthelasma palpebrarum with bichloracetic acid. 806
Evaluation of three different strengths of trichloroacetic acid in xanthelasma palpebrarum. 806
Koebner phenomenon in xanthelasma after treatment with trichloroacetic acid. 806
Cryotherapy may be effective for eyelid xanthoma. 806
Therapeutic effect and pathology changing of eyelid xanthelasma by bleomycin A5. 806
Local corticosteroid treatment of eyelid and orbital xanthogranuloma. 806
Necrobiotic xanthogranuloma treated with chlorambucil. 806
Necrobiotic xanthogranuloma of extremities in an elderly patient successfully treated with low-dose prednisolone. 807
Successful treatment of necrobiotic xanthogranuloma with intravenous immunoglobulin. 807
249 Xeroderma pigmentosum 808
Management strategy 808
Diagnosis 808
Environmental management 808
Social and psychological impact and effect on the family 809
Medical and surgical management 809
Ophthalmologic management 810
Neurologic management 810
Specific investigations 810
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterizes the role of DNA repair. 810
Xeroderma pigmentosum. 810
Shining a light on xeroderma pigmentosum. 810
Hereditary diseases of genome instability and DNA repair. 810
Ocular Manifestations of Xeroderma Pigmentosum: Long-Term Follow-up Highlights the Role of DNA Repair in Protection from Sun Damage. 810
Understanding xeroderma pigmentosum. 810
Growing up in the hospital. 810
A patient’s journey: xeroderma pigmentosum. 811
Auditory analysis of xeroderma pigmentosum, 1971–2012. Hearing function, acute sun sensitivity and DNA repair complementation group predict neurologic degeneration. 811
First-line therapies 811
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype–phenotype relationship. 811
Prevention of skin cancer in xeroderma pigmentosum: the physician as advocate. 811
Total-body cutaneous examination, total-body photography, and dermoscopy in the care of a patient with xeroderma pigmentosum and multiple melanomas. 811
Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2). 811
Second-line therapies 811
Therapeutic response of a brother and sister with xeroderma pigmentosum to imiquimod 5% cream. 811
5% 5-Fluorouracil cream for the treatment of small superficial basal cell carcinoma: efficacy, tolerability, cosmetic outcome and patient satisfaction. 811
Prevention of skin cancer with oral 13-cis retinoic acid in xeroderma pigmentosum. 811
Xeroderma pigmentosum: spinal cord astrocytoma with 9-year survival after radiation and isotretinoin therapy. 811
Topical imiquimod or fluorouracil therapy for basal and squamous cell carcinoma: a systematic review. 811
Third-line therapies 811
Is facial resurfacing with monoblock full-thickness skin graft a remedy in xeroderma pigmentosum? 811
The role of dermabrasion and chemical peels in the treatment of patients with xeroderma pigmentosum. 811
Acknowledgment 811
250 Xerosis 812
Management strategy 812
Specific investigations 812
Sjögren’s syndrome: a retrospective review of the cutaneous features of 93 patients by the Italian Group of Immunodermatology. 812
HIV-associated pruritus: etiology and management. 812
Non infectious skin conditions associated with diabetes mellitus: a prospective study of 308 cases. 812
Eating disorders and the skin. 813
The mucocutaneous manifestations associated with celiac disease in childhood and adolescence. 813
Xerosis from lithium carbonate. 813
First-line therapies 813
Emollients improve treatment results with topical corticosteroids in childhood atopic dermatitis: a randomized comparative study. 813
How useful are soap substitutes? 813
The effect of washing on the thickness of the stratum corneum in normal and atopic individuals. 813
The value of oil baths for adjuvant basic therapy of inflammatory dermatoses with dry, barrier-disrupted skin. 813
A new technique for evaluating bath oil in the treatment of dry skin. 813
Second-line therapies 813
A double blind comparison of two creams containing urea as the active ingredient. Assesment of efficacy and side effects by non invasive techniques and a clinical scoring scheme. 813
Clinical evaluation of 40% urea and 12% ammonium lactate in the treatment of xerosis. 813
A randomized, double-blind, placebo-controlled study to evaluate the efficacy in AD of liquid soap containing 12% ammonium lactate + 20% urea. 813
A controlled two-center study of lactate 12 percent lotion and a petrolatum-based creme in patients with xerosis. 813
Comparative efficacy of 12% ammonium lactate lotion and 5% lactic acid lotion in the treatment of moderate to severe xerosis. 813
A double-blind clinical trial comparing the efficacy and safety of pure lanolin versus ammonium lactate 12% cream for the treatment of moderate to severe foot xerosis. 813
A prospective, randomized, controlled double-blind study of a moisturizer for xerosis of the feet in patients with diabetes. 813
An evaluation of the effect of an alpha hydroxy acid-blend skin cream in the cosmetic improvement of symptoms of moderate to severe xerosis, epidermolytic hyperkeratosis, and ichthyosis. 814
Randomized, double-blind study with glycerol and paraffin in uremic xerosis. 814
Glycerol and the skin: holistic approach to its origin and functions. 814
Xerosis in hypothyroidism: a potential role for the use of topical thyroid hormone in euthyroid patients. 814
Effectiveness of topical Chia seed oil on pruritus of end-stage renal disease (ESRD) patients and healthy volunteers. 814
251 Yellow nail syndrome 815
Management Strategy 815
Specific investigations 815
First-line therapies 815
Combination of fluconazole and α-tocopherol in the treatment of yellow-nail syndrome. 815
Yellow nail syndrome. 815
Yellow nail syndrome in a medical clinic. 815
T and B cell deficiency associated with yellow nail syndrome. 816
Titanium, sinusitis and the yellow nail syndrome. 816
Second-line therapies 816
The yellow nail syndrome (report on 55 cases). 816
A case of yellow nail syndrome with dramatically improved nail discoloration. 816
Syndrome des ongles jaunes d’évolution favorable: rôle de la kinésithérapie respiratoire? 816
Improvement in lymphatic function and partial resolution of nails, after complete decongestive physiotherapy in yellow nail syndrome. 816
Third-line therapy 816
Yellow nail syndrome cured by zinc supplementation. 816
Yellow nail syndrome in a 10-year-old girl. 816
Successful octreotide treatment of chylous pleural effusion and lymphedema in the yellow nail syndrome. 816
Index 817
A 817
B 821
C 823
D 828
E 830
F 832
G 834
H 835
I 837
J 840
K 840
L 840
M 842
N 844
O 846
P 847
Q 851
R 851
S 853
T 856
U 859
V 859
W 860
X 860
Y 861
Z 861