Additional Information
Book Details
Abstract
Ideally suited for rapid reference and efficient, effective recall, Clinical Ophthalmology: A Systematic Approach will keep you up to date with current and evolving practice in the diagnosis and management of ophthalmic disorders, using a visually rich, succinct format that facilitates comprehension for trainees and practitioners. You’ll have access to the latest advances in the field.
- Grasp key information and effectively prepare for examinations with a pictorial, bulleted approach – both highly visual and concise, for more efficient study.
- Move rapidly throughout the text to find the information you need, with color coding and at-a-glance key points.
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Learn from two renowned experts in the field.
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Includes over 2,700 high-quality images, 1,000 of which appear for the first time in this edition.
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Master the latest advances in ophthalmology: radical changes in the management of macular disease, including the widespread introduction of VEGF inhibitor therapy; recent developments in the investigation and treatment of retinal vascular disease; new pharmaceutical interventions for a range of conditions, including infectious eye disease and glaucoma; and updated surgical procedures and methods, including oculoplastic, corneal, and glaucoma surgery.
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Guidance on examination, imaging, and recognition of systemic conditions associated with ocular disease.
Table of Contents
Section Title | Page | Action | Price |
---|---|---|---|
Front cover | cover | ||
Half title page | i | ||
Dedication | ii | ||
Clinical Ophthalmology: A Systematic Approach | iii | ||
Copyright page | iv | ||
Table of Contents | v | ||
Preface to the seventh edition | ix | ||
Chapter 1 Eyelids | 1 | ||
Introduction | 2 | ||
Anatomy | 2 | ||
Epidermis | 2 | ||
Dermis | 3 | ||
Terminology | 3 | ||
Clinical | 3 | ||
Histological | 3 | ||
General considerations | 3 | ||
Benign nodules and cysts | 4 | ||
Chalazion | 4 | ||
Pathogenesis | 4 | ||
Diagnosis | 4 | ||
Treatment | 4 | ||
Other cysts | 4 | ||
Benign epidermal tumours | 4 | ||
Squamous cell papilloma | 4 | ||
Basal cell papilloma | 7 | ||
Actinic keratosis | 7 | ||
Benign pigmented lesions | 8 | ||
Freckle (ephelis) | 8 | ||
Congenital melanocytic naevus | 8 | ||
Acquired melanocytic naevus | 9 | ||
Benign adnexal tumours | 9 | ||
Syringoma | 9 | ||
Pilomatricoma | 10 | ||
Miscellaneous benign tumours | 10 | ||
Capillary haemangioma | 10 | ||
Port-wine stain | 13 | ||
Cutaneous features | 13 | ||
Sturge–Weber syndrome | 13 | ||
Pyogenic granuloma | 14 | ||
Xanthelasma | 14 | ||
Neurofibroma | 15 | ||
Malignant tumours | 15 | ||
Rare predisposing conditions | 15 | ||
Basal cell carcinoma | 16 | ||
General features | 16 | ||
Histology | 16 | ||
Chapter 2 Lacrimal Drainage System | 65 | ||
Anatomy | 66 | ||
Physiology | 66 | ||
Causes of a watering eye | 67 | ||
Evaluation | 67 | ||
External examination | 67 | ||
Fluorescein disappearance test | 67 | ||
Probing and irrigation | 67 | ||
Jones dye testing | 67 | ||
Contrast dacryocystography | 70 | ||
Nuclear lacrimal scintigraphy | 70 | ||
Acquired obstruction | 70 | ||
Primary punctal stenosis | 70 | ||
Secondary punctal stenosis | 70 | ||
Canalicular obstruction | 70 | ||
Nasolacrimal duct obstruction | 71 | ||
Dacryolithiasis | 72 | ||
Congenital obstruction | 72 | ||
Nasolacrimal duct obstruction | 72 | ||
Congenital dacryocele | 73 | ||
Lacrimal surgery | 74 | ||
Conventional dacryocystorhinostomy | 74 | ||
Endoscopic surgery | 75 | ||
Endolaser DCR | 75 | ||
Balloon dacryocystoplasty | 75 | ||
Lester Jones tube | 75 | ||
Chronic canaliculitis | 75 | ||
Diagnosis | 77 | ||
Treatment | 77 | ||
Differential diagnosis | 77 | ||
Dacryocystitis | 77 | ||
Acute dacryocystitis | 77 | ||
Chronic dacryocystitis | 78 | ||
Chapter 3 Orbit | 79 | ||
Introduction | 80 | ||
Anatomy | 80 | ||
Clinical signs | 80 | ||
Soft tissue involvement | 80 | ||
Proptosis | 80 | ||
Enophthalmos | 81 | ||
Dystopia | 82 | ||
Ophthalmoplegia | 82 | ||
Dynamic properties | 82 | ||
Fundus changes | 83 | ||
Special investigations | 84 | ||
Thyroid eye disease | 84 | ||
Introduction | 84 | ||
Thyrotoxicosis | 84 | ||
Risk factors for ophthalmopathy | 84 | ||
Pathogenesis of ophthalmopathy | 84 | ||
Clinical manifestations | 84 | ||
Soft tissue involvement | 85 | ||
Lid retraction | 86 | ||
Pathogenesis | 86 | ||
Signs | 86 | ||
Management | 86 | ||
Proptosis | 87 | ||
Signs | 87 | ||
Management | 87 | ||
Restrictive myopathy | 88 | ||
Diagnosis | 88 | ||
Chapter 4 Dry Eye Disorders | 121 | ||
Definitions | 122 | ||
Physiology | 122 | ||
Tear film constituents | 122 | ||
Spread of the tear film | 122 | ||
Outer lipid layer | 122 | ||
Middle aqueous layer | 122 | ||
Inner mucous layer | 123 | ||
Regulation of tear film components | 123 | ||
Mechanism of disease | 123 | ||
Classification | 123 | ||
Sjögren syndrome | 124 | ||
Clinical features | 124 | ||
Symptoms | 124 | ||
Signs | 125 | ||
Special investigations | 125 | ||
Tear film break-up time | 127 | ||
Schirmer test | 127 | ||
Ocular surface staining | 128 | ||
Other tests | 128 | ||
Treatment | 128 | ||
Patient education | 128 | ||
Tear substitutes | 128 | ||
Mucolytic agents | 129 | ||
Punctal occlusion | 129 | ||
Anti-inflammatory agents | 129 | ||
Contact lenses | 129 | ||
Conservation of existing tears | 130 | ||
Other options | 130 | ||
Chapter 5 Conjunctiva | 131 | ||
Introduction | 132 | ||
Anatomy | 132 | ||
Histology | 132 | ||
Clinical features of conjunctival inflammation | 132 | ||
Symptoms | 132 | ||
Discharge | 132 | ||
Conjunctival reaction | 132 | ||
Lymphadenopathy | 134 | ||
Bacterial conjunctivitis | 135 | ||
Acute bacterial conjunctivitis | 135 | ||
Diagnosis | 135 | ||
Treatment | 135 | ||
Adult chlamydial conjunctivitis | 137 | ||
Pathogenesis | 137 | ||
Urogenital infection | 137 | ||
Diagnosis | 137 | ||
Treatment | 137 | ||
Trachoma | 139 | ||
Pathogenesis | 139 | ||
Diagnosis | 139 | ||
Management | 139 | ||
Neonatal conjunctivitis | 139 | ||
Causes | 139 | ||
Diagnosis | 141 | ||
Treatment | 141 | ||
Viral conjunctivitis | 142 | ||
Adenoviral conjunctivitis | 142 | ||
Pathogenesis | 142 | ||
Presentation | 142 | ||
Signs | 142 | ||
Differential diagnosis | 142 | ||
Management | 142 | ||
Molluscum contagiosum conjunctivitis | 143 | ||
Pathogenesis | 143 | ||
Diagnosis | 144 | ||
Treatment | 144 | ||
Allergic conjunctivitis | 144 | ||
Acute allergic conjunctivitis | 144 | ||
Seasonal and perennial allergic conjunctivitis | 144 | ||
Chapter 6 Cornea | 167 | ||
Introduction | 168 | ||
Anatomy and physiology | 168 | ||
General aspects | 168 | ||
Dimensions | 168 | ||
Layers | 168 | ||
Signs of corneal inflammation | 168 | ||
Superficial lesions | 168 | ||
Deep lesions | 169 | ||
Documentation of clinical signs | 172 | ||
Specular microscopy | 172 | ||
Principles of treatment | 173 | ||
Control of infection and inflammation | 173 | ||
Promotion of epithelial healing | 173 | ||
Bacterial keratitis | 173 | ||
Pathogenesis | 173 | ||
Pathogens | 173 | ||
Risk factors | 175 | ||
Clinical features | 175 | ||
Investigations | 175 | ||
Treatment | 178 | ||
General considerations | 178 | ||
Local therapy | 178 | ||
Systemic antibiotics | 180 | ||
Management of apparent treatment failure | 180 | ||
Fungal keratitis | 180 | ||
Introduction | 180 | ||
Pathogenesis | 180 | ||
Predisposing factors | 180 | ||
Candida and filamentous keratitis | 180 | ||
Clinical features | 180 | ||
Investigations | 181 | ||
Treatment | 182 | ||
Microsporidial keratitis | 182 | ||
Pathogenesis | 182 | ||
Diagnosis | 182 | ||
Treatment | 183 | ||
Herpes simplex keratitis | 183 | ||
Introduction | 183 | ||
Herpes simplex virus (HSV) | 183 | ||
Primary infection | 183 | ||
Recurrent infection | 183 | ||
Epithelial keratitis | 183 | ||
Clinical features | 183 | ||
Treatment | 184 | ||
Disciform keratitis | 185 | ||
Clinical features | 185 | ||
Treatment | 185 | ||
Necrotizing stromal keratitis | 185 | ||
Neurotrophic ulceration | 185 | ||
Other considerations | 186 | ||
Prophylaxis | 186 | ||
Complications | 186 | ||
Keratoplasty | 187 | ||
Herpes zoster ophthalmicus | 187 | ||
Introduction | 187 | ||
Pathogenesis | 187 | ||
Mechanisms of ocular involvement | 187 | ||
Risk of ocular involvement | 187 | ||
Acute shingles | 188 | ||
General features | 188 | ||
Treatment | 188 | ||
Eye disease | 188 | ||
Acute eye disease | 188 | ||
Chronic eye disease | 190 | ||
Relapsing eye disease | 190 | ||
Post-herpetic neuralgia | 190 | ||
Interstitial keratitis | 191 | ||
Pathogenesis | 191 | ||
Chapter 7 Corneal and Refractive Surgery | 239 | ||
Keratoplasty | 240 | ||
Introduction | 240 | ||
General indications | 240 | ||
Donor tissue | 240 | ||
Recipient prognostic factors | 240 | ||
Penetrating keratoplasty | 241 | ||
Technique | 241 | ||
Postoperative management | 241 | ||
Postoperative complications | 242 | ||
Corneal graft rejection | 242 | ||
Superficial lamellar keratoplasty | 244 | ||
Deep anterior lamellar keratoplasty | 244 | ||
Descemet stripping endothelial keratoplasty | 244 | ||
Keratoprostheses | 245 | ||
Refractive procedures | 245 | ||
Introduction | 245 | ||
Correction of myopia | 245 | ||
Correction of hypermetropia (hyperopia) | 245 | ||
Correction of astigmatism | 247 | ||
Correction of presbyopia | 247 | ||
Laser refractive procedures | 247 | ||
Photorefractive keratectomy | 247 | ||
Laser epithelial keratomileusis | 247 | ||
Laser in situ keratomileusis | 247 | ||
Chapter 8 Episclera and Sclera | 251 | ||
Anatomy | 252 | ||
Episcleritis | 252 | ||
Simple episcleritis | 252 | ||
Nodular episcleritis | 252 | ||
Immune-mediated scleritis | 253 | ||
Anterior non-necrotizing scleritis | 253 | ||
Diffuse | 253 | ||
Nodular | 254 | ||
Anterior necrotizing scleritis with inflammation | 255 | ||
Clinical features | 255 | ||
Investigations | 256 | ||
Complications | 256 | ||
Scleromalacia perforans | 257 | ||
Posterior scleritis | 258 | ||
Diagnosis | 258 | ||
Differential diagnosis | 258 | ||
Important systemic associations of scleritis | 259 | ||
Rheumatoid arthritis | 259 | ||
Wegener granulomatosis | 259 | ||
Relapsing polychondritis | 259 | ||
Polyarteritis nodosa | 260 | ||
Treatment of immune-mediated scleritis | 261 | ||
Infectious scleritis | 261 | ||
Causes | 261 | ||
Treatment | 261 | ||
Scleral discoloration | 261 | ||
Alkaptonuria | 261 | ||
Haemochromatosis | 261 | ||
Blue sclera | 262 | ||
Osteogenesis imperfecta | 262 | ||
Type I | 262 | ||
Type IIA | 262 | ||
Ehlers–Danlos syndrome type VI | 262 | ||
Other systemic associations | 263 | ||
Miscellaneous conditions | 263 | ||
Congenital ocular melanocytosis | 263 | ||
Classification | 263 | ||
Clinical features | 264 | ||
Ipsilateral associations | 264 | ||
Idiopathic sclerochoroidal calcification | 264 | ||
Scleral hyaline plaque | 267 | ||
Chapter 9 Lens | 269 | ||
Acquired cataract | 270 | ||
Age-related cataract | 270 | ||
Subcapsular cataract | 270 | ||
Nuclear cataract | 270 | ||
Cortical cataract | 271 | ||
Christmas tree cataract | 271 | ||
Cataract maturity | 271 | ||
Cataract in systemic diseases | 272 | ||
Diabetes mellitus | 272 | ||
Myotonic dystrophy | 273 | ||
Atopic dermatitis | 273 | ||
Neurofibromatosis type 2 | 273 | ||
Secondary cataract | 273 | ||
Chronic anterior uveitis | 273 | ||
Acute congestive angle-closure | 273 | ||
High myopia | 273 | ||
Hereditary fundus dystrophies | 273 | ||
Traumatic cataract | 273 | ||
Management of age-related cataract | 273 | ||
Preoperative considerations | 273 | ||
Indications for surgery | 273 | ||
Systemic preoperative assessment | 273 | ||
Ophthalmic preoperative assessment | 273 | ||
Biometry | 278 | ||
Postoperative refraction | 278 | ||
Intraocular lenses | 279 | ||
Positioning | 279 | ||
Design | 280 | ||
Anaesthesia | 280 | ||
Phacoemulsification | 281 | ||
Introduction | 281 | ||
Phacodynamics | 281 | ||
Pumps | 282 | ||
Handpiece | 282 | ||
Viscoelastics | 282 | ||
Technique | 283 | ||
Small incision manual cataract surgery | 285 | ||
Operative complications | 285 | ||
Rupture of the posterior lens capsule | 285 | ||
Posterior loss of lens fragments | 288 | ||
Posterior dislocation of IOL | 288 | ||
Suprachoroidal haemorrhage | 288 | ||
Acute postoperative endophthalmitis | 289 | ||
Pathogenesis | 289 | ||
Prophylaxis | 290 | ||
Clinical features | 290 | ||
Differential diagnosis | 290 | ||
Identification of pathogens | 290 | ||
Treatment | 291 | ||
Subsequent management | 293 | ||
Delayed-onset postoperative endophthalmitis | 293 | ||
Pathogenesis | 293 | ||
Diagnosis | 293 | ||
Posterior capsular opacification | 295 | ||
Signs | 295 | ||
Treatment | 296 | ||
Anterior capsular fibrosis and contraction | 296 | ||
Miscellaneous postoperative complications | 296 | ||
Malposition of IOL | 296 | ||
Cystoid macular oedema | 296 | ||
Retinal detachment | 298 | ||
Congenital cataract | 298 | ||
Aetiology | 298 | ||
Inheritance | 298 | ||
Morphology | 298 | ||
Systemic metabolic associations | 298 | ||
Galactoasemia | 298 | ||
Lowe syndrome | 301 | ||
Fabry disease | 301 | ||
Mannosidosis | 301 | ||
Other metabolic disorders | 301 | ||
Associated intrauterine infections | 302 | ||
Congenital rubella | 302 | ||
Toxoplasmosis | 302 | ||
Cytomegalovirus infection | 302 | ||
Varicella | 302 | ||
Associated chromosomal abnormalities | 302 | ||
Down syndrome (trisomy 21) | 302 | ||
Edwards syndrome (trisomy 18) | 302 | ||
Cri du chat syndrome (partial deletion of 5p) | 302 | ||
Associated skeletal syndromes | 302 | ||
Hallermann–Streiff–François syndrome | 302 | ||
Nance–Horan syndrome | 302 | ||
Management | 303 | ||
Ocular examination | 303 | ||
Systemic investigations | 303 | ||
Treatment | 303 | ||
Postoperative complications | 303 | ||
Visual rehabilitation | 304 | ||
Ectopia lentis | 304 | ||
Without systemic associations | 304 | ||
With systemic associations | 304 | ||
Marfan syndrome | 304 | ||
Weill–Marchesani syndrome | 306 | ||
Homocystinuria | 306 | ||
Other systemic associations | 306 | ||
Management | 307 | ||
Abnormalities of shape | 308 | ||
Anterior lenticonus | 308 | ||
Posterior lenticonus | 308 | ||
Lentiglobus | 309 | ||
Microspherophakia | 309 | ||
Microphakia | 309 | ||
Coloboma | 309 | ||
Chapter 10 Glaucoma | 311 | ||
Introduction | 312 | ||
Aqueous secretion | 312 | ||
Aqueous outflow | 312 | ||
Anatomy | 312 | ||
Physiology | 312 | ||
Intraocular pressure | 313 | ||
Concept of normal intraocular pressure | 313 | ||
Fluctuation | 313 | ||
Overview of glaucoma | 313 | ||
Definition | 313 | ||
Epidemiology | 313 | ||
Classification | 313 | ||
Tonometry | 313 | ||
Goldmann tonometry | 313 | ||
Principles | 313 | ||
Technique | 314 | ||
Sources of error | 314 | ||
Other types of tonometry | 315 | ||
Gonioscopy | 316 | ||
Introduction | 316 | ||
Overview | 316 | ||
Optical principles | 316 | ||
Indirect gonioscopy | 316 | ||
Non-indentation gonioscopy | 317 | ||
Indentation gonioscopy | 317 | ||
Direct gonioscopy | 318 | ||
Identification of angle structures | 319 | ||
Grading of angle width | 320 | ||
Shaffer system | 320 | ||
Other systems | 322 | ||
Pathological findings | 323 | ||
Evaluation of the optic nerve head | 323 | ||
Normal optic nerve head | 323 | ||
Neuroretinal rim | 323 | ||
Optic disc size | 323 | ||
Cup–disc ratio | 323 | ||
Changes in glaucoma | 324 | ||
Optic nerve head | 324 | ||
Subtypes of glaucomatous damage | 324 | ||
Non-specific signs of glaucomatous damage | 324 | ||
Peripapillary changes | 327 | ||
Retinal nerve fibre layer | 327 | ||
Imaging in glaucoma | 327 | ||
Stereo disc photography | 327 | ||
Confocal scanning laser tomography | 327 | ||
Scanning laser polarimetry | 330 | ||
Optical coherence tomography | 331 | ||
Anterior chamber depth measurement | 331 | ||
Perimetry | 331 | ||
Definitions | 331 | ||
Types of perimetry | 333 | ||
Kinetic | 333 | ||
Static | 333 | ||
Suprathreshold | 333 | ||
Threshold | 333 | ||
Sources of error | 333 | ||
Humphrey Field Analyzer | 334 | ||
Testing patterns | 334 | ||
Testing strategies | 334 | ||
Displays | 334 | ||
Reliability indices | 336 | ||
Glaucoma hemifield test | 336 | ||
Global indices | 337 | ||
Computer analysis of serial fields | 338 | ||
Short-wave automated perimetry | 338 | ||
Frequency-doubling contrast test | 338 | ||
Ocular hypertension | 338 | ||
Definition | 338 | ||
Risk factors for developing glaucoma | 339 | ||
Pre-perimetric glaucoma | 340 | ||
Management | 340 | ||
Primary open-angle glaucoma | 340 | ||
Introduction | 340 | ||
Definition | 340 | ||
Risk factors | 340 | ||
Genetics | 341 | ||
Steroid responsiveness | 341 | ||
Pathogenesis of glaucomatous optic neuropathy | 341 | ||
Screening | 341 | ||
Diagnosis | 341 | ||
History | 341 | ||
Examination | 342 | ||
Visual field defects | 342 | ||
Management | 343 | ||
Patient instruction | 343 | ||
Treatment goals | 344 | ||
Medical therapy | 344 | ||
Laser trabeculoplasty | 346 | ||
Surgery | 346 | ||
Prognosis | 346 | ||
Normal-pressure glaucoma | 346 | ||
Definition | 346 | ||
Pathogenesis | 346 | ||
Risk factors | 347 | ||
Differential diagnosis | 347 | ||
Diagnosis | 347 | ||
Treatment | 347 | ||
Primary angle-closure glaucoma | 348 | ||
Introduction | 348 | ||
Overview | 348 | ||
Classification | 348 | ||
Mechanism | 348 | ||
Risk factors | 350 | ||
Diagnosis | 350 | ||
Symptoms | 350 | ||
Signs | 350 | ||
Provocation testing | 351 | ||
Treatment | 351 | ||
Primary angle-closure suspect (PACS) | 351 | ||
Chronic presentation of PAC and PACG | 351 | ||
Acute and subacute presentation of PAC and PACG | 351 | ||
Differential diagnosis of an acute elevation of IOP | 353 | ||
Classification of secondary glaucoma | 353 | ||
Open-angle | 353 | ||
Angle-closure | 354 | ||
Pseudoexfoliation | 355 | ||
Pseudoexfoliation syndrome | 355 | ||
Introduction | 355 | ||
Chapter 11 Uveitis | 401 | ||
Introduction | 402 | ||
Anatomical classification | 402 | ||
Definitions | 402 | ||
Clinical features | 402 | ||
Acute anterior uveitis | 402 | ||
Chronic anterior uveitis | 404 | ||
Posterior uveitis | 406 | ||
Special investigations | 406 | ||
Indications | 406 | ||
Skin tests | 407 | ||
Serology | 407 | ||
Syphilis | 407 | ||
Toxoplasmosis | 408 | ||
Enzyme assay | 408 | ||
HLA tissue typing | 409 | ||
Imaging | 409 | ||
Radiology | 410 | ||
Biopsy | 410 | ||
Principles of treatment | 410 | ||
General principles | 410 | ||
Mydriatics | 410 | ||
Preparations | 410 | ||
Indications | 410 | ||
Topical steroids | 411 | ||
Indications | 411 | ||
Complications | 411 | ||
Periocular steroid injection | 411 | ||
Intraocular steroids | 411 | ||
Systemic steroids | 412 | ||
Antimetabolites | 412 | ||
Indications | 412 | ||
Azathioprine | 412 | ||
Methotrexate | 413 | ||
Mycophenolate mofetil | 413 | ||
Calcineurin inhibitors | 413 | ||
Ciclosporin | 413 | ||
Tacrolimus | 413 | ||
Biological blockers | 413 | ||
Intermediate uveitis | 413 | ||
Overview | 413 | ||
Diagnosis | 413 | ||
Course | 415 | ||
Complications | 415 | ||
Treatment | 415 | ||
Systemic associations | 415 | ||
Differential diagnosis | 415 | ||
Uveitis in spondyloarthropathies | 415 | ||
HLA-B27 and spondyloarthropathies | 415 | ||
Ankylosing spondylitis | 416 | ||
Reiter syndrome | 416 | ||
Psoriatic arthritis | 416 | ||
Uveitis in juvenile arthritis | 416 | ||
Juvenile idiopathic arthritis | 416 | ||
Overview | 416 | ||
Arthritis | 418 | ||
Anterior uveitis | 418 | ||
Differential diagnosis | 418 | ||
Familial juvenile systemic granulomatosis syndrome | 420 | ||
Uveitis in bowel disease | 420 | ||
Ulcerative colitis | 420 | ||
Crohn disease | 420 | ||
Whipple disease | 422 | ||
Uveitis in renal disease | 422 | ||
Tubulointerstitial nephritis and uveitis (TINU) | 422 | ||
IgA glomerulonephritis | 422 | ||
Sarcoidosis | 422 | ||
Definition | 422 | ||
Presentation | 422 | ||
Pulmonary disease | 422 | ||
Skin lesions | 422 | ||
Other manifestations | 422 | ||
Investigations | 424 | ||
Ocular features | 424 | ||
Behçet syndrome | 426 | ||
Overview | 426 | ||
Diagnostic criteria | 426 | ||
Additional features | 427 | ||
Ocular features | 427 | ||
Treatment of posterior uveitis | 428 | ||
Differential diagnosis | 429 | ||
Toxoplasmosis | 429 | ||
Introduction | 429 | ||
Pathogenesis | 429 | ||
Mode of human infection | 430 | ||
Congenital toxoplasmosis | 430 | ||
Acquired toxoplasmosis | 430 | ||
Toxoplasma retinitis | 430 | ||
Pathogenesis | 430 | ||
Clinical features | 431 | ||
Complications | 433 | ||
Treatment | 433 | ||
Toxocariasis | 433 | ||
Pathogenesis | 433 | ||
Chronic endophthalmitis | 435 | ||
Posterior pole granuloma | 435 | ||
Peripheral granuloma | 435 | ||
Miscellaneous parasitic uveitis | 436 | ||
Onchocerciasis | 436 | ||
Pathogenesis | 436 | ||
Systemic features | 436 | ||
Ocular features | 437 | ||
Cysticercosis | 438 | ||
Diffuse unilateral subacute neuroretinitis | 439 | ||
Choroidal pneumocystosis | 440 | ||
Uveitis in acquired immunodeficiency syndrome | 441 | ||
Introduction | 441 | ||
Pathogenesis | 441 | ||
Systemic features | 441 | ||
Serology | 442 | ||
Treatment | 442 | ||
Ocular features | 442 | ||
HIV microangiopathy | 442 | ||
Cytomegalovirus retinitis | 442 | ||
Clinical features | 443 | ||
Systemic treatment | 443 | ||
Intravitreal treatment | 444 | ||
Prognosis | 444 | ||
Progressive retinal necrosis | 444 | ||
Miscellaneous viral uveitis | 445 | ||
Acute retinal necrosis | 445 | ||
Herpes simplex anterior uveitis | 445 | ||
Varicella zoster anterior uveitis | 445 | ||
Congenital rubella | 446 | ||
Subacute sclerosing panencephalitis | 447 | ||
Fungal uveitis | 447 | ||
Presumed ocular histoplasmosis syndrome | 447 | ||
Pathogenesis | 447 | ||
General signs | 447 | ||
Exudative maculopathy | 447 | ||
Cryptococcosis | 449 | ||
Pathogenesis | 449 | ||
Systemic features | 449 | ||
Ocular features | 449 | ||
Endogenous fungal endophthalmitis | 449 | ||
Coccidioidomycosis | 450 | ||
Bacterial uveitis | 450 | ||
Tuberculosis | 450 | ||
Pathogenesis | 450 | ||
Anterior segment involvement | 450 | ||
Tuberculous uveitis | 450 | ||
Syphilis | 451 | ||
Pathogenesis | 451 | ||
Stages | 452 | ||
Syphilitic uveitis | 452 | ||
Lyme disease | 452 | ||
Brucellosis | 454 | ||
Endogenous bacterial endophthalmitis | 454 | ||
Cat-scratch disease | 456 | ||
Leprosy | 456 | ||
white dot syndromes | 457 | ||
Multiple evanescent white dot syndrome | 457 | ||
Acute idiopathic blind spot enlargement syndrome | 458 | ||
Acute posterior multifocal placoid pigment epitheliopathy | 458 | ||
Multifocal choroiditis and panuveitis | 459 | ||
Punctate inner choroidopathy | 460 | ||
Serpiginous choroidopathy | 461 | ||
Progressive subretinal fibrosis and uveitis syndrome | 461 | ||
Acute macular neuroretinopathy | 462 | ||
Acute zonal occult outer retinopathy | 463 | ||
Primary stromal choroiditis | 464 | ||
Vogt–Koyanagi–Harada syndrome | 464 | ||
Pathogenesis | 464 | ||
Phases | 465 | ||
Uveitis | 465 | ||
Sympathetic ophthalmitis | 465 | ||
Birdshot retinochoroidopathy | 467 | ||
Miscellaneous anterior uveitis | 469 | ||
Fuchs uveitis syndrome | 469 | ||
Lens-induced uveitis | 469 | ||
Phacoanaphylactic endophthalmitis | 469 | ||
Phacogenic non-granulomatous uveitis | 471 | ||
Miscellaneous posterior uveitis | 471 | ||
Acute retinal pigment epitheliitis | 471 | ||
Acute idiopathic maculopathy | 472 | ||
Acute multifocal retinitis | 473 | ||
Solitary idiopathic choroiditis | 473 | ||
Frosted branch angiitis | 473 | ||
Idiopathic retinal vasculitis, aneurysms and neuroretinitis syndrome | 473 | ||
Chapter 12 Ocular Tumours | 475 | ||
Benign epibulbar tumours | 476 | ||
Conjunctival naevus | 476 | ||
Conjunctival papilloma | 476 | ||
Dermoid | 476 | ||
Diagnosis | 476 | ||
Systemic associations | 476 | ||
Dermolipoma | 479 | ||
Pyogenic granuloma | 480 | ||
Conjunctival epithelial melanosis | 480 | ||
Miscellaneous tumours | 481 | ||
Malignant and premalignant epibulbar tumours | 481 | ||
Primary acquired melanosis | 481 | ||
Melanoma | 482 | ||
Diagnosis | 482 | ||
Treatment | 483 | ||
Prognosis | 483 | ||
Ocular surface squamous neoplasia | 483 | ||
Definition | 483 | ||
Diagnosis | 483 | ||
Treatment | 486 | ||
Lymphoproliferative lesions | 486 | ||
Kaposi sarcoma | 486 | ||
Iris tumours | 486 | ||
Iris naevus | 486 | ||
Iris melanoma | 486 | ||
Overview | 486 | ||
Diagnosis | 486 | ||
Treatment | 487 | ||
Metastatic tumours | 488 | ||
Miscellaneous tumours | 488 | ||
Iris cysts | 488 | ||
Primary | 488 | ||
Secondary | 492 | ||
Ciliary body tumours | 492 | ||
Ciliary body melanoma | 492 | ||
Signs | 493 | ||
Investigations | 493 | ||
Treatment | 495 | ||
Differential diagnosis | 495 | ||
Medulloepithelioma | 495 | ||
Tumours of the choroid | 496 | ||
Choroidal naevus | 496 | ||
Histology | 496 | ||
Signs | 496 | ||
Investigations | 496 | ||
Atypical naevus | 496 | ||
Suspicious naevus | 496 | ||
Differential diagnosis | 496 | ||
Choroidal melanoma | 496 | ||
Pathology | 496 | ||
Adverse prognostic factors | 498 | ||
Signs | 498 | ||
Special investigations | 498 | ||
Systemic investigations | 501 | ||
Principles of treatment | 501 | ||
Brachytherapy | 502 | ||
External beam radiotherapy | 503 | ||
Stereotactic radiotherapy | 503 | ||
Transpupillary thermotherapy | 503 | ||
Trans-scleral choroidectomy | 503 | ||
Enucleation | 503 | ||
Differential diagnosis | 503 | ||
Circumscribed choroidal haemangioma | 504 | ||
Diagnosis | 504 | ||
Treatment | 504 | ||
Differential diagnosis | 504 | ||
Diffuse choroidal haemangioma | 504 | ||
Optic disc melanocytoma | 504 | ||
Choroidal osteoma | 506 | ||
Diagnosis | 506 | ||
Differential diagnosis | 506 | ||
Metastatic tumours | 506 | ||
Diagnosis | 507 | ||
Systemic investigations | 510 | ||
Management | 510 | ||
Neural retinal tumours | 510 | ||
Retinoblastoma | 510 | ||
Pathology | 510 | ||
Genetics | 510 | ||
Presentation | 512 | ||
Signs | 513 | ||
Investigations | 513 | ||
Treatment of small tumours | 513 | ||
Treatment of medium-size tumours | 513 | ||
Treatment of large tumours | 513 | ||
Treatment of extraocular extension | 513 | ||
Follow-up | 515 | ||
Differential diagnosis | 516 | ||
Astrocytoma | 517 | ||
Diagnosis | 518 | ||
Tuberous sclerosis | 518 | ||
Vascular retinal tumours | 520 | ||
Capillary haemangioma | 520 | ||
Overview | 520 | ||
Diagnosis | 520 | ||
Treatment | 522 | ||
Von Hippel–Lindau syndrome | 522 | ||
Cavernous haemangioma | 523 | ||
Racemose haemangioma | 523 | ||
Vasoproliferative tumour | 524 | ||
PRIMArY Intraocular lymphoma | 525 | ||
Overview | 525 | ||
Ocular features | 525 | ||
Neurological features | 526 | ||
Investigations | 527 | ||
Treatment | 527 | ||
Tumours of the retinal pigment epithelium | 527 | ||
Typical congenital hypertrophy of the RPE | 527 | ||
Atypical congenital hypertrophy of the RPE | 527 | ||
Signs | 527 | ||
Systemic associations | 527 | ||
Combined hamartoma of the retina and RPE | 527 | ||
Congenital hamartoma of the RPE | 528 | ||
Paraneoplastic syndromes | 529 | ||
Bilateral diffuse uveal melanocytic proliferation | 529 | ||
Cancer-associated retinopathy | 531 | ||
Melanoma-associated retinopathy | 531 | ||
Chapter 13 Retinal Vascular Disease | 533 | ||
Retinal circulation | 534 | ||
Arterial system | 534 | ||
Capillaries | 534 | ||
Venous system | 534 | ||
Diabetic retinopathy | 534 | ||
Introduction | 534 | ||
Prevalence | 534 | ||
Risk factors | 534 | ||
Pathogenesis | 535 | ||
Classification | 536 | ||
Signs | 536 | ||
Microaneurysms | 536 | ||
Retinal haemorrhages | 536 | ||
Exudates | 536 | ||
Diabetic macular oedema | 537 | ||
Focal maculopathy | 539 | ||
Diffuse maculopathy | 541 | ||
Ischaemic maculopathy | 541 | ||
Clinically significant macular oedema | 541 | ||
Cotton wool spots | 541 | ||
Venous changes | 542 | ||
Intraretinal microvascular abnormalities | 542 | ||
Arterial changes | 543 | ||
Proliferative retinopathy | 543 | ||
Treatment | 543 | ||
Argon laser treatment of clinically significant macular oedema | 543 | ||
Other treatments for maculopathy | 545 | ||
Laser photocoagulation for proliferative retinopathy | 546 | ||
VEGF inhibition for proliferative retinopathy | 549 | ||
Advanced diabetic eye disease | 549 | ||
Diagnosis | 549 | ||
Indications for pars plana vitrectomy | 550 | ||
Visual results of pars plana vitrectomy | 551 | ||
Retinal venous occlusive disease | 551 | ||
Pathogenesis | 551 | ||
Predisposing factors | 551 | ||
Common | 551 | ||
Uncommon | 551 | ||
Systemic assessment | 552 | ||
All patients | 552 | ||
Selected patients according to clinical indication | 552 | ||
Branch retinal vein occlusion | 552 | ||
Classification | 552 | ||
Diagnosis | 553 | ||
Prognosis | 553 | ||
Further management | 553 | ||
Treatment of macular oedema | 554 | ||
Treatment of neovascularization | 555 | ||
Impending central retinal vein occlusion | 555 | ||
Non-ischaemic central retinal vein occlusion | 555 | ||
Diagnosis | 555 | ||
Follow-up | 556 | ||
Prognosis | 556 | ||
Treatment of macular oedema | 557 | ||
Ischaemic central retinal vein occlusion | 557 | ||
Diagnosis | 557 | ||
Prognosis | 557 | ||
Follow up | 557 | ||
Treatment of neovascularization | 558 | ||
Papillophlebitis | 558 | ||
Diagnosis | 558 | ||
Prognosis | 559 | ||
Hemiretinal vein occlusion | 559 | ||
Systemic treatment in retinal vein occlusion | 559 | ||
Retinal arterial occlusive disease | 559 | ||
Aetiology | 559 | ||
Atherosclerosis-related thrombosis | 559 | ||
Carotid embolism | 559 | ||
Uncommon causes | 561 | ||
Systemic assessment | 561 | ||
All patients | 561 | ||
Selected patients | 562 | ||
Amaurosis fugax | 562 | ||
Branch retinal artery occlusion | 562 | ||
Diagnosis | 562 | ||
Follow-up | 563 | ||
Prognosis | 563 | ||
Central retinal artery occlusion | 563 | ||
Diagnosis | 563 | ||
Follow-up | 564 | ||
Prognosis | 564 | ||
Cilioretinal artery occlusion | 564 | ||
Treatment of acute retinal artery occlusion | 564 | ||
Systemic prophylaxis following retinal arterial occlusion | 565 | ||
Asymptomatic retinal embolus | 566 | ||
Ocular ischaemic syndrome | 566 | ||
Pathogenesis | 566 | ||
Diagnosis | 566 | ||
Management | 566 | ||
Differential diagnosis | 566 | ||
Hypertensive disease | 567 | ||
Retinopathy | 567 | ||
Signs | 567 | ||
Choroidopathy | 568 | ||
Sickle-cell retinopathy | 569 | ||
Sickling haemoglobinopathies | 569 | ||
Proliferative retinopathy | 570 | ||
Diagnosis | 570 | ||
Treatment | 570 | ||
Differential diagnosis of peripheral retinal neovascularization | 572 | ||
Non-proliferative retinopathy | 572 | ||
Asymptomatic lesions | 572 | ||
Symptomatic lesions | 572 | ||
Anterior segment features | 572 | ||
Retinopathy of prematurity | 573 | ||
Pathogenesis | 573 | ||
Active disease | 573 | ||
Location | 573 | ||
Extent | 574 | ||
Staging | 574 | ||
Other features | 574 | ||
Regression | 576 | ||
Screening | 576 | ||
Treatment | 576 | ||
Cicatricial disease | 576 | ||
Retinal artery macroaneurysm | 576 | ||
Diagnosis | 576 | ||
Prognosis | 579 | ||
Management | 579 | ||
Primary retinal telangiectasiA | 580 | ||
Idiopathic macular telangiectasia | 581 | ||
Type 1: aneurysmal telangiectasia | 581 | ||
Type 2: perafoveal telangiectasia | 581 | ||
Occlusive telangiectasia | 582 | ||
Coats disease | 582 | ||
Diagnosis | 582 | ||
Treatment | 583 | ||
Prognosis | 583 | ||
Differential diagnosis | 583 | ||
Eales disease | 583 | ||
Radiation retinopathy | 586 | ||
Purtscher retinopathy | 586 | ||
Benign idiopathic haemorrhagic retinopathy | 586 | ||
Valsalva retinopathy | 588 | ||
Lipaemia retinalis | 588 | ||
Retinopathy in blood disorders | 589 | ||
Leukaemia | 589 | ||
Classification | 589 | ||
Ocular features | 589 | ||
Anaemia | 589 | ||
Hyperviscosity | 590 | ||
Congenital vascular anomalies | 591 | ||
Retinal macrovessel | 591 | ||
Arteriovenous communications | 592 | ||
Chapter 14 Acquired Macular Disorders | 593 | ||
Introduction | 594 | ||
Anatomical landmarks | 594 | ||
Retinal pigment epithelium | 594 | ||
Bruch membrane | 595 | ||
Clinical evaluation of macular disease | 595 | ||
Symptoms | 595 | ||
Slit-lamp biomicroscopy | 595 | ||
Visual acuity | 596 | ||
Snellen visual acuity | 596 | ||
Very poor visual acuity | 596 | ||
LogMAR acuity | 597 | ||
LogMar charts | 597 | ||
Contrast sensitivity | 598 | ||
Amsler grid | 598 | ||
Charts | 599 | ||
Technique | 600 | ||
fundus Fluorescein angiography | 601 | ||
Principles | 601 | ||
Technique | 602 | ||
Phases of the angiogram | 603 | ||
Causes of hyperfluorescence | 604 | ||
Causes of hypofluorescence | 604 | ||
Systematic approach to reporting angiograms | 608 | ||
Indocyanine green angiography | 608 | ||
Principles | 608 | ||
Adverse effects | 609 | ||
Causes of hyperfluorescence | 611 | ||
Hypofluorescence | 611 | ||
Clinical indications | 611 | ||
Optical coherence tomography | 611 | ||
Definition | 611 | ||
Principles | 611 | ||
Indications | 611 | ||
Normal appearance | 611 | ||
Age-related macular degeneration | 611 | ||
Introduction | 611 | ||
Classification | 612 | ||
Epidemiology | 612 | ||
Risk factors | 613 | ||
Drusen | 613 | ||
Histopathology | 613 | ||
Clinical features | 614 | ||
Fluorescein angiography | 614 | ||
Lesions related to drusen | 614 | ||
Prophylactic antioxidant supplementation in AMD | 615 | ||
Recommendations for use | 615 | ||
Regimen | 616 | ||
Other considerations | 616 | ||
Non-exudative (dry) AMD | 616 | ||
Diagnosis | 616 | ||
Management | 616 | ||
Retinal pigment epithelial detachment | 616 | ||
Pathogenesis | 616 | ||
Serous PED | 616 | ||
Fibrovascular PED | 619 | ||
Drusenoid PED | 619 | ||
Haemorrhagic PED | 619 | ||
Retinal pigment epithelial tear | 619 | ||
Choroidal neovascularization | 620 | ||
Pathogenesis | 620 | ||
Clinical features | 621 | ||
Fluorescein angiography | 621 | ||
Indocyanine green angiography | 622 | ||
Optical coherence tomography | 623 | ||
Treatment with anti-VEGF agents | 623 | ||
Ranibizumab (Lucentis) | 624 | ||
Bevacizumab (Avastin) | 624 | ||
Pegaptanib (Macugen) | 624 | ||
Technique of intravitreal injection | 625 | ||
Photodynamic therapy (PDT) | 625 | ||
Combination therapies | 626 | ||
Argon laser photocoagulation | 626 | ||
Experimental treatments | 626 | ||
Haemorrhagic AMD | 627 | ||
Retinal angiomatous proliferation | 627 | ||
Diagnosis | 627 | ||
Treatment | 628 | ||
Polypoidal choroidal vasculopathy | 628 | ||
Overview | 628 | ||
Diagnosis | 628 | ||
Treatment | 629 | ||
Age-related macular hole | 629 | ||
Overview | 629 | ||
Pathogenesis | 629 | ||
Stages | 629 | ||
Investigations | 629 | ||
Surgery | 629 | ||
Differential diagnosis of age-related macular hole | 631 | ||
Macular microhole | 631 | ||
Central serous chorioretinopathy | 632 | ||
Overview | 632 | ||
Clinical features | 632 | ||
Investigations | 633 | ||
Course | 633 | ||
Management | 633 | ||
Cystoid macular oedema | 633 | ||
Pathogenesis | 633 | ||
Diagnosis | 633 | ||
Causes | 635 | ||
Epimacular membrane | 635 | ||
Pathogenesis | 635 | ||
Classification | 635 | ||
Diagnosis | 636 | ||
Management | 636 | ||
Degenerative myopia | 637 | ||
Pathogenesis | 637 | ||
Diagnosis | 637 | ||
Complications | 637 | ||
Angioid streaks | 641 | ||
Ocular considerations | 641 | ||
Histology | 641 | ||
Diagnosis | 641 | ||
Complications | 641 | ||
Systemic associations | 641 | ||
Pseudoxanthoma elasticum | 641 | ||
Occasional associations | 643 | ||
Choroidal folds | 643 | ||
Pathogenesis | 643 | ||
Causes | 643 | ||
Chapter 15 Hereditary Fundus Dystrophies | 647 | ||
Introduction | 648 | ||
Applied anatomy | 648 | ||
Inheritance | 648 | ||
Classification | 648 | ||
Investigations | 648 | ||
Electroretinography | 648 | ||
Principles | 648 | ||
Standard ERG | 649 | ||
Multifocal ERG | 649 | ||
Electro-oculography | 649 | ||
Dark adaptometry | 650 | ||
Colour vision tests | 650 | ||
Principles | 650 | ||
Colour vision tests | 651 | ||
Generalized photoreceptor dystrophies | 651 | ||
Typical retinitis pigmentosa | 651 | ||
Inheritance | 651 | ||
Diagnosis | 652 | ||
Ocular associations | 654 | ||
Atypical retinitis pigmentosa | 654 | ||
Important systemic associations | 654 | ||
Bassen–Kornzweig syndrome (abetalipoproteinaemia) | 654 | ||
Refsum disease | 654 | ||
Kearns–Sayre syndrome | 654 | ||
Bardet–Biedl syndrome | 655 | ||
Usher syndrome | 655 | ||
Progressive cone dystrophy | 656 | ||
Leber congenital amaurosis | 656 | ||
Stargardt disease and fundus flavimaculatus | 657 | ||
Bietti corneoretinal crystalline dystrophy | 660 | ||
Alport syndrome | 661 | ||
Familial benign fleck retina | 661 | ||
Pigmented paravenous chorioretinal atrophy | 661 | ||
Congenital stationary night blindness | 662 | ||
With normal fundus | 662 | ||
With abnormal fundus | 662 | ||
Congenital monochromatism (achromatopsia) | 664 | ||
Rod monochromatism (complete achromatopsia) | 664 | ||
Blue cone monochromatism (incomplete achromatopsia) | 665 | ||
Macular dystrophies | 665 | ||
Juvenile Best macular dystrophy | 665 | ||
Multifocal vitelliform lesions without Best disease | 665 | ||
Pattern dystrophy | 665 | ||
Adult-onset macular vitelliform dystrophy | 665 | ||
Butterfly-shaped macular dystrophy | 665 | ||
Multifocal pattern dystrophy simulating fundus flavimaculatus | 665 | ||
Macroreticular pattern dystrophy | 667 | ||
North Carolina macular dystrophy | 667 | ||
Familial dominant drusen | 668 | ||
Sorsby pseudoinflammatory dystrophy | 669 | ||
Benign concentric annular macular dystrophy | 669 | ||
Central areolar choroidal dystrophy | 670 | ||
Dominant cystoid macular oedema | 670 | ||
Sjögren–Larsson syndrome | 670 | ||
Familial internal limiting membrane dystrophy | 670 | ||
Generalized choroidal dystrophies | 670 | ||
Choroideremia | 670 | ||
Gyrate atrophy | 671 | ||
Generalized choroidal dystrophy | 674 | ||
Progressive bifocal chorioretinal atrophy | 674 | ||
Vitreoretinal dystrophies | 674 | ||
Juvenile X-linked retinoschisis | 674 | ||
Pathogenesis | 674 | ||
Diagnosis | 674 | ||
Stickler syndrome | 675 | ||
Classification | 675 | ||
Systemic features | 675 | ||
Ocular features | 676 | ||
Wagner syndrome | 676 | ||
Familial exudative vitreoretinopathy | 678 | ||
Enhanced S-cone syndrome and Goldmann–Favre syndrome | 678 | ||
Snowflake vitreoretinal degeneration | 679 | ||
Dominant neovascular inflammatory vitreoretinopathy | 679 | ||
Dominant vitreoretinochoroidopathy | 681 | ||
Kniest dysplasia | 681 | ||
Albinism | 681 | ||
Introduction | 681 | ||
Tyrosinase-negative oculocutaneous albinism | 682 | ||
Tyrosinase-positive oculocutaneous albinism | 683 | ||
Ocular features | 683 | ||
Associated systemic syndromes | 683 | ||
Ocular albinism | 683 | ||
Cherry-red spot at macula | 683 | ||
Pathogenesis | 683 | ||
GM1 gangliosidosis (generalized) | 684 | ||
Mucolipidosis type I (sialidosis) | 684 | ||
GM2 gangliosidosis | 684 | ||
Tay–Sachs disease | 684 | ||
Sandhoff disease | 684 | ||
Niemann–Pick disease | 684 | ||
Type A (acute neuronopathic) | 685 | ||
Type B (chronic non-neuronopathic) | 685 | ||
Farber disease | 685 | ||
Chapter 16 Retinal Detachment | 687 | ||
Introduction | 688 | ||
Anatomy of the peripheral retina | 688 | ||
Pars plana | 688 | ||
Ora serrata | 688 | ||
Vitreous base | 688 | ||
Innocuous peripheral retinal degenerations | 689 | ||
Definitions | 689 | ||
Retinal detachment | 689 | ||
Vitreous adhesions | 689 | ||
Vitreoretinal traction | 690 | ||
Posterior vitreous detachment | 690 | ||
Retinal break | 691 | ||
Clinical examination | 692 | ||
Head-mounted indirect ophthalmoscopy | 692 | ||
Scleral indentation | 693 | ||
Goldmann three-mirror examination | 693 | ||
Fundus drawing | 694 | ||
Finding the primary break | 696 | ||
Ultrasonography | 697 | ||
Principles | 697 | ||
Technique | 698 | ||
Rhegmatogenous retinal detachment | 698 | ||
Pathogenesis | 698 | ||
Dynamic vitreoretinal traction | 698 | ||
Complications of acute PVD | 698 | ||
Lattice degeneration | 700 | ||
Snailtrack degeneration | 701 | ||
Degenerative retinoschisis | 701 | ||
‘White with pressure’ and ‘white without pressure’ | 702 | ||
Diffuse chorioretinal atrophy | 703 | ||
Significance of myopia | 703 | ||
Symptoms | 704 | ||
Signs | 705 | ||
General | 705 | ||
Fresh retinal detachment | 707 | ||
Long-standing retinal detachment | 707 | ||
Proliferative vitreoretinopathy | 708 | ||
Differential diagnosis | 709 | ||
Degenerative retinoschisis | 709 | ||
Uveal effusion syndrome | 709 | ||
Choroidal detachment | 709 | ||
Prophylaxis | 710 | ||
Characteristics of break | 710 | ||
Other considerations | 711 | ||
Clinical examples | 712 | ||
Choice of treatment modalities | 713 | ||
Technique of laser photocoagulation | 713 | ||
Technique of cryotherapy | 713 | ||
Causes of failure | 714 | ||
Surgery | 715 | ||
Indications for urgent surgery | 715 | ||
Choice of technique | 715 | ||
Pneumatic retinopexy | 715 | ||
Principles of scleral buckling | 715 | ||
Technique of scleral buckling | 717 | ||
Drainage of subretinal fluid | 717 | ||
Fresh retinal detachment | 719 | ||
Long-standing retinal detachment | 720 | ||
Causes of failure | 720 | ||
Tractional retinal detachment | 721 | ||
Pathogenesis of diabetic tractional retinal detachment | 721 | ||
Diagnosis | 721 | ||
Exudative retinal detachment | 722 | ||
Pathogenesis | 722 | ||
Diagnosis | 722 | ||
Treatment | 723 | ||
Pars plana vitrectomy | 723 | ||
Introduction | 723 | ||
Instrumentation | 723 | ||
Tamponading agents | 724 | ||
Indications | 725 | ||
Rhegmatogenous retinal detachment | 725 | ||
Tractional retinal detachment | 725 | ||
Technique | 725 | ||
Basic vitrectomy | 725 | ||
Closure of giant tears | 725 | ||
Proliferative vitreoretinopathy | 725 | ||
Tractional retinal detachment | 727 | ||
Postoperative complications | 727 | ||
Raised intraocular pressure | 727 | ||
Cataract | 728 | ||
Band keratopathy | 728 | ||
Chapter 17 Vitreous Opacities | 729 | ||
Introduction | 730 | ||
Muscae volitantes | 730 | ||
Vitreous haemorrhage | 730 | ||
Asteroid hyalosis (Benson disease) | 730 | ||
Synchisis scintillans (cholesterolosis bulbi) | 730 | ||
Amyloidosis | 730 | ||
Vitreous cyst | 733 | ||
Chapter 18 Strabismus | 735 | ||
Introduction | 736 | ||
Definitions | 736 | ||
Anatomy of extraocular muscles | 736 | ||
Principles | 736 | ||
Horizontal rectus muscles | 737 | ||
Vertical rectus muscles | 737 | ||
Spiral of Tillaux | 738 | ||
Oblique muscles | 738 | ||
Muscle pulleys | 739 | ||
Nerve supply | 739 | ||
Ocular movements | 739 | ||
Ductions | 739 | ||
Versions | 739 | ||
Vergences | 740 | ||
Positions of gaze | 740 | ||
Laws of ocular motility | 741 | ||
Sensory considerations | 741 | ||
Basic aspects | 741 | ||
Sensory adaptations to strabismus | 744 | ||
Suppression | 744 | ||
Abnormal retinal correspondence | 744 | ||
Microtropia | 745 | ||
Consequences of strabismus | 745 | ||
Motor adaptation to strabismus | 745 | ||
Amblyopia | 745 | ||
Classification | 745 | ||
Diagnosis | 746 | ||
Treatment | 746 | ||
Clinical evaluation | 746 | ||
History | 746 | ||
Visual acuity | 747 | ||
Testing in preverbal children | 747 | ||
Testing in verbal children | 747 | ||
Tests for stereopsis | 748 | ||
TNO | 748 | ||
Frisby | 748 | ||
Lang | 748 | ||
Titmus | 749 | ||
Frisby–Davis distance stereotest | 750 | ||
Tests for binocular fusion in infants without manifest squint | 750 | ||
Base-out prism | 750 | ||
Binocular convergence | 750 | ||
Tests for sensory anomalies | 750 | ||
Worth four-dot | 750 | ||
Bagolini striated glasses | 751 | ||
4 Δ prism test | 752 | ||
Synoptophore | 753 | ||
Grades of binocular vision | 754 | ||
Detection of abnormal retinal correspondence | 754 | ||
Measurement of deviation | 755 | ||
Hirschberg test | 755 | ||
Krimsky and prism reflection tests | 755 | ||
Cover–uncover test | 755 | ||
Alternate cover test | 757 | ||
Prism cover test | 757 | ||
Maddox wing | 758 | ||
Maddox rod | 758 | ||
Motility tests | 758 | ||
Ocular movements | 758 | ||
Near point of convergence | 758 | ||
Near point of accommodation | 758 | ||
Fusional amplitudes | 759 | ||
Postoperative diplopia test | 759 | ||
Investigation of diplopia | 759 | ||
Electronic Hess test | 760 | ||
Lees screen | 760 | ||
Changes with time | 761 | ||
Clinical examples | 761 | ||
Refraction and fundoscopy | 763 | ||
Cycloplegia | 763 | ||
Change of refraction | 764 | ||
When to prescribe | 764 | ||
Heterophoria | 765 | ||
Vergence abnormalities | 765 | ||
Convergence insufficiency | 765 | ||
Divergence insufficiency | 765 | ||
Near reflex insufficiency | 765 | ||
Spasm of the near reflex | 765 | ||
Esotropia | 765 | ||
Early-onset esotropia | 766 | ||
Signs | 766 | ||
Initial treatment | 766 | ||
Subsequent treatment | 767 | ||
Differential diagnosis | 768 | ||
Accommodative esotropia | 768 | ||
Refractive accommodative esotropia | 768 | ||
Non-refractive accommodative esotropia | 768 | ||
Treatment | 769 | ||
Microtropia | 770 | ||
Other esotropias | 770 | ||
Near esotropia (non-accommodative convergence excess) | 770 | ||
Distance esotropia | 770 | ||
Acute (late-onset) esotropia | 770 | ||
Secondary (sensory) esotropia | 770 | ||
Consecutive esotropia | 770 | ||
Cyclic esotropia | 771 | ||
High myopia esotropia | 771 | ||
Exotropia | 771 | ||
Constant (early-onset) exotropia | 771 | ||
Intermittent exotropia | 771 | ||
Diagnosis | 771 | ||
Classification | 771 | ||
Treatment | 771 | ||
Sensory exotropia | 772 | ||
Consecutive exotropia | 772 | ||
Special syndromes | 772 | ||
Duane retraction syndrome | 772 | ||
Signs | 772 | ||
Classification (Huber) | 773 | ||
Treatment | 773 | ||
Brown syndrome | 773 | ||
Classification | 774 | ||
Diagnosis | 774 | ||
Treatment | 774 | ||
Monocular elevator deficit | 774 | ||
Möbius syndrome | 774 | ||
Congenital fibrosis of the extraocular muscles | 774 | ||
Strabismus fixus | 774 | ||
Alphabet patterns | 774 | ||
‘V’ pattern | 776 | ||
Causes | 776 | ||
Treatment | 776 | ||
‘A’ pattern | 777 | ||
Causes | 777 | ||
Treatment | 777 | ||
Surgery | 778 | ||
Weakening procedures | 778 | ||
Recession | 778 | ||
Disinsertion | 778 | ||
Posterior fixation suture | 779 | ||
Strengthening procedures | 779 | ||
Treatment of paretic strabismus | 779 | ||
Lateral rectus palsy | 779 | ||
Superior oblique palsy | 779 | ||
Adjustable sutures | 780 | ||
Indications | 780 | ||
Initial steps | 780 | ||
Postoperative adjustment | 780 | ||
Botulinum toxin chemodenervation | 780 | ||
Chapter 19 Neuro-ophthalmology | 783 | ||
Neuroimaging | 784 | ||
Computed tomography | 784 | ||
Physics | 784 | ||
Contrast enhancement | 784 | ||
Indications | 784 | ||
Magnetic resonance imaging | 785 | ||
Physics | 785 | ||
Weighting | 785 | ||
Contrast enhancement | 785 | ||
Limitations | 785 | ||
Neuro-ophthalmic indications | 785 | ||
Angiography | 788 | ||
Magnetic resonance angiography | 788 | ||
Computed tomographic angiography | 788 | ||
Computed tomographic venography | 789 | ||
Conventional catheter angiography | 789 | ||
Optic nerve | 789 | ||
Anatomy | 789 | ||
General structure | 789 | ||
Anatomical subdivisions | 789 | ||
Visual evoked potential | 790 | ||
Signs of optic nerve dysfunction | 790 | ||
Optic atrophy | 790 | ||
Primary optic atrophy | 790 | ||
Secondary optic atrophy | 791 | ||
Consecutive optic atrophy | 791 | ||
Classification of optic neuritis | 791 | ||
Ophthalmoscopic classification | 791 | ||
Aetiological classification | 792 | ||
Demyelinating optic neuritis | 792 | ||
Overview | 792 | ||
Multiple sclerosis | 792 | ||
Association between optic neuritis and multiple sclerosis | 793 | ||
Clinical features of demyelinating optic neuritis | 793 | ||
Treatment of demyelinating optic neuritis | 794 | ||
Parainfectious optic neuritis | 794 | ||
Infectious optic neuritis | 794 | ||
Non-infectious optic neuritis | 794 | ||
Sarcoid | 794 | ||
Autoimmune | 795 | ||
Neuroretinitis | 795 | ||
Non-arteritic anterior ischaemic optic neuropathy | 796 | ||
Arteritic anterior ischaemic optic neuropathy | 796 | ||
Diagnosis of giant cell arteritis | 796 | ||
Treatment of giant cell arteritis | 798 | ||
Ophthalmic manifestations of giant cell arteritis | 798 | ||
Arteritic anterior ischaemic optic neuropathy | 798 | ||
Other manifestations | 798 | ||
Posterior ischaemic optic neuropathy | 798 | ||
Diabetic papillopathy | 798 | ||
Leber hereditary optic neuropathy | 799 | ||
Hereditary optic atrophy | 799 | ||
Kjer-type optic atrophy | 799 | ||
Behr syndrome | 800 | ||
Wolfram syndrome | 800 | ||
Nutritional optic neuropathy | 800 | ||
Papilloedema | 801 | ||
Pathogenesis | 801 | ||
Cerebrospinal fluid and causes of raised intracranial pressure | 801 | ||
Diagnosis of raised intracranial pressure | 801 | ||
Stages of papilloedema | 802 | ||
Congenital optic disc anomalies | 802 | ||
Tilted disc | 802 | ||
Optic disc pit | 803 | ||
Optic disc drusen | 805 | ||
Optic disc coloboma | 805 | ||
Morning glory anomaly | 808 | ||
Optic nerve hypoplasia | 808 | ||
Myelinated nerve fibres | 809 | ||
Aicardi syndrome | 810 | ||
Miscellaneous anomalies | 810 | ||
Pupillary reactions | 812 | ||
Anatomy | 812 | ||
Light reflex | 812 | ||
Near reflex | 812 | ||
Afferent pupillary defect | 812 | ||
Absolute afferent pupillary defect | 812 | ||
Relative afferent pupillary defect | 812 | ||
Oculosympathetic palsy (Horner syndrome) | 813 | ||
Anatomy | 813 | ||
Causes | 813 | ||
Signs | 814 | ||
Pharmacological tests | 814 | ||
Adie pupil | 815 | ||
Other abnormal reactions | 815 | ||
Light-near dissociation | 815 | ||
Chiasm | 816 | ||
Anatomy | 816 | ||
Pituitary gland | 816 | ||
Chiasmal neural pathways | 816 | ||
Anatomical variants | 817 | ||
Parachiasmal vascular structures | 817 | ||
Physiology | 822 | ||
Pituitary hormones | 822 | ||
Causes of hypopituitarism | 822 | ||
Pituitary adenomas | 823 | ||
Basophil adenoma | 823 | ||
Acidophil adenoma | 824 | ||
Chromophobe adenoma | 824 | ||
Special investigations of pituitary adenomas | 825 | ||
Treatment of pituitary adenomas | 826 | ||
Craniopharyngioma | 826 | ||
Meningioma | 826 | ||
Retrochiasmal pathways | 827 | ||
Optic tract | 827 | ||
Overview | 827 | ||
Incongruity | 827 | ||
Clinical features | 827 | ||
Optic radiations | 828 | ||
Anatomy | 828 | ||
Temporal radiations | 828 | ||
Anterior parietal radiations | 828 | ||
Main radiations | 829 | ||
Striate cortex | 829 | ||
Clinical features | 829 | ||
Causes | 830 | ||
Ocular motor nerves | 830 | ||
3rd nerve | 830 | ||
Nuclear complex | 830 | ||
Fasciculus | 830 | ||
Basilar | 830 | ||
Intracavernous | 830 | ||
Intraorbital | 831 | ||
Pupillomotor fibres | 832 | ||
Signs | 832 | ||
Aberrant regeneration | 832 | ||
Causes of isolated 3rd nerve palsy | 832 | ||
Treatment | 833 | ||
4th nerve | 833 | ||
Anatomy | 833 | ||
Signs | 834 | ||
Bilateral involvement | 834 | ||
Special tests | 834 | ||
Causes of isolated 4th nerve palsy | 835 | ||
6th nerve | 835 | ||
Nucleus | 835 | ||
Fasciculus | 836 | ||
Basilar | 837 | ||
Intracavernous and intraorbital | 837 | ||
Signs | 837 | ||
Differential diagnosis | 838 | ||
Supranuclear disorders of ocular motility | 838 | ||
Conjugate eye movements | 838 | ||
Saccadic movements | 838 | ||
Smooth pursuit movements | 838 | ||
Non-optical reflexes | 839 | ||
Horizontal gaze palsy | 839 | ||
Anatomy | 839 | ||
Signs | 839 | ||
Vertical gaze palsy | 840 | ||
Anatomy | 840 | ||
Parinaud (dorsal midbrain) syndrome | 840 | ||
Progressive supranuclear palsy | 841 | ||
Nystagmus | 841 | ||
Introduction | 841 | ||
Physiological principles | 841 | ||
Classification | 841 | ||
Physiological nystagmus | 841 | ||
Vestibular nystagmus | 842 | ||
Motor imbalance nystagmus | 843 | ||
Primary congenital nystagmus | 843 | ||
Spasmus nutans | 843 | ||
Latent nystagmus | 844 | ||
Periodic alternating nystagmus | 844 | ||
Convergence-retraction nystagmus | 844 | ||
Downbeat nystagmus | 844 | ||
Upbeat nystagmus | 844 | ||
See-saw nystagmus | 845 | ||
Ataxic nystagmus | 845 | ||
Bruns nystagmus | 845 | ||
Sensory deprivation nystagmus | 845 | ||
Surgery for nystagmus | 845 | ||
Nystagmoid movements | 846 | ||
Ocular flutter and opsoclonus | 846 | ||
Ocular bobbing | 846 | ||
Carotid stenosis | 846 | ||
Diagnosis | 846 | ||
Treatment | 847 | ||
Intracranial aneurysms | 847 | ||
Anatomy | 847 | ||
Neurological considerations | 847 | ||
Neuro-ophthalmic considerations | 848 | ||
Ocular motor nerve palsies | 848 | ||
Visual loss | 849 | ||
Terson syndrome | 849 | ||
Ocular myopathies | 849 | ||
Myasthenia gravis | 849 | ||
Systemic myasthenia | 849 | ||
Ocular myasthenia | 850 | ||
Edrophonium test | 850 | ||
Myotonic dystrophy | 852 | ||
Chronic progressive external ophthalmoplegia | 852 | ||
Signs | 852 | ||
Kearns–Sayre syndrome | 852 | ||
Oculopharyngeal dystrophy | 853 | ||
Eaton–Lambert myasthenic syndrome | 854 | ||
Neurofibromatosis | 854 | ||
Neurofibromatosis type 1 | 854 | ||
Diagnostic criteria | 854 | ||
Systemic features | 854 | ||
Ophthalmic features | 854 | ||
Neurofibromatosis type 2 | 854 | ||
Diagnostic criteria | 855 | ||
Ophthalmic features | 855 | ||
Migraine | 855 | ||
Clinical features | 855 | ||
Common migraine | 856 | ||
Classical migraine | 856 | ||
Cluster headache | 857 | ||
Other types of migraine | 858 | ||
Treatment | 858 | ||
Differential diagnosis | 858 | ||
Visual phenomena | 858 | ||
Neuralgias | 858 | ||
Facial spasm | 859 | ||
Essential blepharospasm | 859 | ||
Clinical features | 859 | ||
Treatment | 859 | ||
Hemifacial spasm | 860 | ||
Chapter 20 Ocular Side-effects of Systemic Medication | 861 | ||
Cornea | 862 | ||
Vortex keratopathy | 862 | ||
Chlorpromazine | 863 | ||
Argyrosis | 863 | ||
Chrysiasis | 863 | ||
Amantadine | 863 | ||
Lens | 863 | ||
Steroids | 863 | ||
Other drugs | 863 | ||
Uveitis | 863 | ||
Rifabutin | 863 | ||
Cidofovir | 864 | ||
Retina | 864 | ||
Antimalarials | 864 | ||
Drugs | 864 | ||
Retinopathy | 864 | ||
Screening | 865 | ||
Phenothiazines | 865 | ||
Drug-induced crystalline maculopathies | 866 | ||
Other drugs | 866 | ||
Optic nerve | 868 | ||
Ethambutol | 868 | ||
Amiodarone | 869 | ||
Vigabatrin | 869 | ||
Topiramate | 869 | ||
Chapter 21 Trauma | 871 | ||
Eyelid trauma | 872 | ||
Periocular haematoma | 872 | ||
Laceration | 872 | ||
Orbital fractures | 873 | ||
Blow-out orbital floor fracture | 873 | ||
Diagnosis | 873 | ||
Treatment | 874 | ||
Blow-out medial wall fracture | 875 | ||
Roof fracture | 875 | ||
Lateral wall fracture | 877 | ||
Trauma to the globe | 877 | ||
Introduction | 877 | ||
Definitions | 877 | ||
Principles of evaluation | 877 | ||
Blunt trauma | 878 | ||
Corneal | 878 | ||
Hyphaema | 879 | ||
Anterior uvea | 879 | ||
Intraocular pressure | 880 | ||
Lenticular | 881 | ||
Globe rupture | 881 | ||
Vitreous haemorrhage | 881 | ||
Commotio retinae | 882 | ||
Choroidal rupture | 882 | ||
Retinal breaks and detachment | 884 | ||
Optic nerve | 884 | ||
Shaken baby syndrome | 885 | ||
Penetrating trauma | 885 | ||
Causes | 885 | ||
Corneal | 886 | ||
Scleral | 886 | ||
Retinal detachment | 886 | ||
Superficial foreign bodies | 886 | ||
Subtarsal | 886 | ||
Corneal | 887 | ||
Intraocular foreign bodies | 888 | ||
Initial management | 889 | ||
Technique of removal | 889 | ||
Siderosis | 889 | ||
Chalcosis | 890 | ||
Enucleation | 891 | ||
Bacterial endophthalmitis | 891 | ||
Chemical injuries | 891 | ||
Causes | 891 | ||
Pathophysiology | 891 | ||
Management | 892 | ||
Emergency treatment | 892 | ||
Grading of severity | 893 | ||
Medical treatment | 894 | ||
Surgery | 895 | ||
Index | 897 |