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Atlas of Gynecologic Surgical Pathology E-Book

Atlas of Gynecologic Surgical Pathology E-Book

Philip B. Clement | Robert H. Young

(2013)

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Book Details

Abstract

Rapidly and accurately identify gynecologic tumors and related lesions with the updated Atlas of Gynecologic Surgical Pathology. Complete with hundreds of stunning photographs and now available with online access, this visually dynamic medical reference book provides you with the know-how you need to perform state-of-the-art gynecologic diagnoses, right at your own microscope.

  • Consult this title on your favorite e-reader, conduct rapid searches, and adjust font sizes for optimal readability. Compatible with Kindle®, nook®, and other popular devices.
  • Quickly and effortlessly find the essential information you need with summary tables, charts, and boxes throughout the text.
  • Expedite reference with a consistent approach to every entity discussed, including definitions, clinical features, gross features, microscopic features, and differential diagnoses.
  • Avoid diagnostic errors with comprehensive coverage of commonly encountered pitfalls.
  • Overcome today's toughest diagnostic challenges with guidance from internationally recognized experts in gynecologic pathology.
  • Stay completely current on the newest disease entities and updated classification schemes, and take advantage of nearly 1,000 brand-new references.
  • Ensure diagnostic accuracy and gain absolute visual clarity with the addition of 100 images.
  • Remain at the forefront of the most recently developed diagnostic methods, such as immunohistochemical diagnosis for malignant lesions and differential diagnosis of neoplastic and pseudoneoplastic lesions.
  • Access the complete contents online at Expert Consult.

Table of Contents

Section Title Page Action Price
Front cover cover
Atlas of Gynecologic Surgical Pathology i
Copyright page iv
Table of Contents v
Dedication vi
Preface to the Third Edition ix
References ix
Glossary of Abbreviations and Acronyms x
1 Non-neoplastic Lesions and Benign Tumors of the Vulva 1
Viral Infections 2
Human Papillomavirus (HPV) Infection INCLUDING Condyloma Acuminatum 2
Clinical and gross features (Fig. 1.1) 2
Histological features (Figs. 1.2–1.4) 2
Differential diagnosis 3
Herpes Virus Infection (Fig. 1.5) 4
Other Viral Infections 4
References 4
Human papillomavirus infection 4
Herpes virus infection 4
Other viral infections 5
Other Infections 5
Syphilis 5
Granuloma Inguinale 5
Lymphogranuloma Venereum 5
Chancroid 5
Tuberculosis 5
Necrotizing Fasciitis and Progressive Bacterial Synergistic Gangrene 6
Other Bacterial Infections 6
Fungal Infections and Parasitic Infestations 6
References 6
Non-Neoplastic Epithelial Disorders 7
Classification* 7
Lichen Sclerosus 7
Clinical and gross features (Fig. 1.6) 7
Microscopic features (Figs. 1.7 and 1.8) 7
Differential diagnosis 8
Behavior 8
Squamous Cell Hyperplasia, NOS (Fig. 1.9) 8
Other Dermatoses (Fig. 1.10) 8
References 9
Squamous Papillomatosis (Fig. 1.11) 10
References 10
Pigmented Lesions 10
Lentigo Simplex and Melanosis (Fig. 1.12) 10
Usual Melanocytic Nevi 11
1 Abstracts and Keywords e1
Abstract: e1
Keywords: e1
2 Malignant Tumors of the Vulva 29
Squamous Cell Carcinoma and Its Precursors 30
Vulvar Intraepithelial Neoplasia (VIN) 30
Terminology 30
Clinical features of usual VIN 30
Pathological features of usual VIN and its variants (Figs. 2.1–2.8) 30
Behavior of usual VIN 32
Clinical features of differentiated VIN 32
Microscopic features of differentiated VIN (Figs. 2.9–2.11) 32
Behavior of differentiated VIN 33
Differential diagnosis of usual and differentiated VIN 33
Invasive Squamous Cell Carcinoma of Usual Type 34
Clinical features 34
Pathologic features (Figs. 2.12–2.18) 34
Differential diagnosis 36
Behavior and prognostic factors 36
Verrucous Carcinoma (Figs. 2.19–2.20) 37
Sarcomatoid Squamous Cell Carcinoma (Fig. 2.21) 37
Other Rare Variants of Squamous Cell Carcinoma 37
References 38
Vulvar intraepithelial neoplasia 38
Invasive squamous cell carcinoma: general features 39
Invasive squamous cell carcinoma: behavior and prognostic factors 39
Verrucous carcinoma 39
Sarcomatoid squamous cell carcinoma 40
Other rare variants of squamous cell carcinoma 40
Paget’s Disease 40
Clinical features (Fig. 2.22) 40
Histogenesis 40
Microscopic features (Figs. 2.23–2.28) 40
Differential diagnosis 42
Behavior 42
References 42
Carcinoma of Bartholin’s Gland (Figs. 2.29–2.30) 43
References 43
Other Adenocarcinomas and Related Tumors 44
Adenocarcinoma of Mammary Type (Fig. 2.31) 44
Adenocarcinomas of Skin Appendage Origin (Fig. 2.32) 44
Rare Miscellaneous Adenocarcinomas, Malignant Myoepithelioma, and Carcinoid Tumor 44
References 45
Adenocarcinoma of mammary type 45
Adenocarcinomas of skin appendage origin 45
Rare miscellaneous adenocarcinomas, malignant myoepithelioma, and carcinoid tumor 45
Basal Cell Carcinoma (Fig. 2.33) 45
2 Abstracts and Keywords e2
Abstract: e2
Keywords: e2
3 The Vagina 53
Tumor-Like Lesions 53
Condyloma Acuminatum 53
Vaginal Adenosis (Figs. 3.1–3.6) 53
Cysts (Fig. 3.7) 55
Prolapse of Fallopian Tube (Fig. 3.8) 55
Postoperative Spindle Cell Nodule 56
3 Abstracts and Keywords e3
Abstract: e3
Keywords: e3
4 Tumor-like Lesions and Benign Tumors of the Uterine Cervix 73
Tumor-Like Lesions 74
Metaplasias and Ectopias 74
Squamous Metaplasia (Figs. 4.1–4.2) 74
Transitional Cell Metaplasia (Fig. 4.3) 74
Tubal, Tuboendometrioid, and Endometrioid Metaplasia 75
General features 75
Microscopic features (Figs. 4.4–4.6) 75
Differential diagnosis 75
Endometriosis (Figs. 4.7–4.8) 76
Endocervicosis (Figs. 4.9–4.10) 77
Endosalpingiosis (Fig. 4.11) 77
Deep Glands and Cysts (Figs. 4.12–4.13) 78
Intestinal Metaplasia 78
Oxyphilic Metaplasia (Fig. 4.14) 78
Ectopic Prostatic Tissue and Ectopic Skene’s Glands (Figs. 4.15–4.16) 78
Other Ectopias (Figs. 4.17–4.18) 79
Endocervical Glandular Hyperplasias 79
Tunnel Clusters (Figs. 4.19–4.20) 79
Microglandular Hyperplasia (Figs. 4.21–4.23) 80
Diffuse Laminar Endocervical Glandular Hyperplasia (Fig. 4.24) 81
Lobular Endocervical Glandular Hyperplasia (Figs. 4.25–4.26) 82
Differential diagnosis 82
Adenoid Basal Hyperplasia (Fig. 4.27) 82
Mesonephric Lesions 83
Mesonephric Remnants (Fig. 4.28) 83
Mesonephric Hyperplasia (Figs. 4.29–4.30) 83
Mesonephric Ductal Hyperplasia (Fig. 4.31) 84
Reactive and Reparative Lesions 84
Postbiopsy Pseudoinvasion of Squamous Epithelium (Fig. 4.32) 84
Reactive and Reparative Atypia (Fig. 4.33) 84
Pagetoid Dyskeratosis 85
Radiation-induced Atypia (Fig. 4.34) 85
Changes Secondary to Extravasation of Mucin (Fig. 4.35) 85
Postoperative Spindle Cell Nodule 86
Pseudoactinomycotic Radiate Granules 86
Inflammatory Lesions 86
Typical Cervicitis 86
Papillary Endocervicitis (Fig. 4.36) 86
Follicular Cervicitis (Fig. 4.37) 86
Florid Reactive Lymphoid Hyperplasia (Lymphoma-like Lesion) (Figs. 4.38–4.39) 86
Plasma Cell Cervicitis 87
Histiocytic Infiltrates and Noninfectious Granulomas (Fig. 4.40) 87
Changes Related to Cautery and Monsel’s Solution (Figs. 4.41–4.44) 87
Eosinophilic Cervicitis 88
Ligneous Cervicitis (Fig. 4.45) 88
Pyoderma Gangrenosum 89
Arteritis (Fig. 4.46) 89
Infectious Lesions 89
Viral Lesions (Figs. 4.47–4.48) 89
Bacterial Lesions 90
Parasitic Lesions 90
Pregnancy-Related Changes 90
Ectopic Decidua (Fig. 4.49) 90
Arias-Stella Reaction (Fig. 4.50) 90
Placental Site Nodules and Plaques 91
Cervical Pregnancy (Fig. 4.51) 91
Melanotic Lesions 91
Blue Nevus (Fig. 4.52) 91
Mucosal Melanosis 91
Miscellaneous Tumor-Like Lesions 91
Multinucleated Stromal Giant Cells (Fig. 4.53) 91
Signet-ring-like Epithelial Cells 92
Amyloidosis 92
Psammomatous Calcification (Fig. 4.54) 92
Myxoid Change 92
Extramedullary Hematopoiesis 92
References 92
Transitional cell metaplasia 92
Tubal and tuboendometrioid metaplasia 92
Endometriosis 93
Endocervicosis 93
Endosalpingiosis 93
Deep glands and cysts 93
Intestinal metaplasia 93
Oxyphilic metaplasia 93
Ectopic prostatic tissue and ectopic Skene’s glands 93
Other ectopias 93
Tunnel clusters 93
Microglandular hyperplasia 93
Diffuse laminar endocervical glandular hyperplasia 93
Lobular endocervical glandular hyperplasia 93
Adenoid basal hyperplasia 94
Mesonephric hyperplasia 94
Postbiopsy pseudoinvasion of squamous epithelium 94
Reactive and reparative atypia 94
Pagetoid dyskeratosis 94
Radiation-induced atypia 94
Pseudoactinomycotic radiate granules 94
Follicular cervicitis 94
Florid reactive lymphoid hyperplasia (lymphoma-like lesion) 94
Plasma cell cervicitis 94
Histiocytic infiltrates and noninfectious granulomas 94
Changes related to cautery and Monsel’s solution 95
Eosinophilic cervicitis 95
Ligneous cervicitis 95
Pyoderma gangrenosum 95
Arteritis 95
Viral lesions 95
Bacterial lesions 95
Parasitic lesions 95
Ectopic decidua 95
Arias-Stella reaction 95
Cervical pregnancy 95
Mucosal melanosis 95
Multinucleated stromal giant cells 95
Signet-ring-like epithelial cells 95
Amyloidosis 95
Psammomatous calcification 96
Benign Tumors 96
Epithelial 96
Endocervical Polyps (see Figs. 4.1, 4.21, 4.55, 4.56) 96
Squamous Papilloma 97
Inverted Transitional Cell Papilloma 97
Müllerian Papilloma 97
Mixed Epithelial and Mesenchymal Tumors 97
Adenofibroma 97
Villous and Villoglandular Adenoma 97
Adenomyoma of Endocervical Type (Figs. 4.57–4.59) 97
Differential diagnosis 98
Mesenchymal Tumors 98
References 98
Endocervical polyps 98
Squamous papilloma 99
Inverted transitional cell papilloma 99
Müllerian papilloma 99
Villous and villoglandular adenomas 99
Adenomyoma of endocervical type 99
Mesenchymal tumors 99
4 Abstracts and Keywords e4
Abstract: e4
Keywords: e4
5 Invasive Squamous Cell Carcinoma of the Cervix and its Precursors 100
Precursor Lesions 100
Classification 100
Risk factors 100
Clinical features (Fig. 5.1) 101
Microscopic features of LSILs (Figs. 5.2–5.8) 101
Microscopic features of HSILs (Figs. 5.9–5.17) 102
Topography of SILs 105
Features of SILs suggesting the presence of early invasion 105
Differential diagnosis of SILs (Figs. 5.18–5.23) 105
Natural history 107
References 108
General 108
SILs of unusual types and locations, atypias, and metaplastic lesions 108
Immunohistochemistry and molecular findings 108
SUPERFICIALLY Invasive Squamous Cell Carcinomas (Stage IA) 109
Clinical features 109
Microscopic features (Figs. 5.24–5.26) 110
Differential diagnosis 110
Prognosis and behavior of Ia1 lesions 110
Prognosis and behavior of Ia2 lesions 111
References 111
Invasive Squamous Cell Carcinoma 111
Clinical features 111
Gross features (Fig. 5.27) 111
Usual microscopic features (Figs. 5.28–5.30) 111
Unusual microscopic features (Figs. 5.31–5.34) 112
Differential diagnosis 114
Prognostic factors 114
References 115
General and prognostic 115
Unusual subtypes and findings 115
Variants of Squamous Cell Carcinoma 116
Basaloid Squamous Cell Carcinoma (Fig. 5.35) 116
Verrucous Carcinoma 116
Warty or Condylomatous Carcinoma 116
Papillary Squamous Cell Carcinoma (Figs. 5.36–5.37) 116
Lymphoepithelioma-like Carcinoma (Fig. 5.38) 117
Papillary Transitional Cell Carcinoma and Squamotransitional Cell Carcinomas (Fig. 5.39) 117
Sarcomatoid Squamous Cell Carcinoma (Fig. 5.40) 118
Mucoepidermoid Carcinoma 118
References 118
Basaloid squamous cell carcinoma 118
Verrucous carcinoma 118
Papillary squamous cell carcinoma 118
Lymphoepithelioma-like carcinoma 118
Papillary transitional cell carcinoma and squamotransitional cell carcinomas 119
Sarcomatoid squamous cell carcinoma 119
Mucoepidermoid carcinoma 119
5 Abstracts and Keywords e5
Abstract: e5
Keywords: e5
6 Adenocarcinomas of the Cervix, Related Tumors, and Their Precursors 120
Preinvasive Glandular Lesions and Early Invasive Adenocarcinomas 120
Adenocarcinoma in Situ (AIS) 120
Clinical features 120
Microscopic features (Figs. 6.1–6.7) 121
Evidence supporting precancerous potential 123
Differential diagnosis 123
Behavior 123
Endocervical Glandular Dysplasia (EGD) 123
Early Invasive Adenocarcinoma (Stage Ia Adenocarcinoma) 123
Microscopic features (Figs. 6.8–6.9) 124
Behavior 124
References 125
Adenocarcinoma in situ 125
Endocervical glandular dysplasia (EGD) 125
Early invasive adenocarcinoma 125
Invasive Adenocarcinomas 126
Clinical findings and prognostic features 126
Endocervical Adenocarcinoma, Usual Type (Figs. 6.10–6.19) 127
Differential diagnosis 129
Variant: Well-differentiated Villoglandular Adenocarcinoma (Figs. 6.20–6.21) 130
Mucinous Carcinomas, including Gastric-type Adenocarcinoma (Figs. 6.22–6.23) 130
Differential diagnosis 131
Variant: Adenoma Malignum (Minimal Deviation Adenocarcinoma) (Figs. 6.24–6.29) 132
Variant: Intestinal-type Adenocarcinomas, Including Signet-ring Cell Adenocarcinoma and Colloid Adenocarcinoma (Fig. 6.30) 133
Endometrioid Adenocarcinoma (Fig. 6.31) 134
Differential diagnosis 134
Variant: Minimal Deviation Endometrioid Adenocarcinoma (Fig. 6.32) 134
Clear Cell Adenocarcinoma (Figs. 6.33–6.34) 135
Differential diagnosis 135
Serous Adenocarcinoma (Fig. 6.35) 135
Differential diagnosis 136
Mesonephric Adenocarcinoma and Malignant Mixed Mesonephric Tumors (Fig. 6.36) 136
Differential diagnosis 137
Adenosquamous Carcinoma (Figs. 6.37–6.38) 137
Glassy Cell Carcinoma (Fig. 6.39) 138
Adenoid Basal Carcinoma (Adenoid Basal Epithelioma) (Figs. 6.40–6.44) 138
Differential diagnosis 140
Adenoid Cystic Carcinoma (Figs. 6.45–6.46) 140
Differential diagnosis 141
References 141
Clinical findings and prognostic features 141
Endocervical adenocarcinoma of usual type 141
Well-differentiated villoglandular adenocarcinoma 141
Mucinous carcinomas including gastric-type adenocarcinomas 142
Intestinal-type adenocarcinomas, including signet-ring cell adenocarcinoma and colloid adenocarcinoma 142
Endometrioid adenocarcinoma 142
Clear cell adenocarcinoma 142
Serous adenocarcinoma 142
Mesonephric adenocarcinoma 143
Adenosquamous carcinoma 143
Glassy cell carcinoma 143
Adenoid basal carcinoma 143
Adenoid cystic carcinoma 143
Neuroendocrine Tumors 144
Typical and Atypical Carcinoid Tumors 144
Small Cell (Neuroendocrine) Carcinoma 144
Clinical features 144
Pathological features (Figs. 6.47–6.48) 144
Differential diagnosis 145
Behavior and prognostic factors 145
Large Cell Neuroendocrine Carcinoma (Figs. 6.49–6.52) 145
Differential diagnosis 146
References 146
Typical and atypical carcinoid tumors 146
Small cell (neuroendocrine) carcinoma 146
Large cell neuroendocrine carcinoma 147
Metastatic adenocarcinomas (see Chapter 10) 147
6 Abstracts and Keywords e6
Abstract: e6
Keywords: e6
7 Non-neoplastic Lesions of the Uterine Corpus 148
Changes Related to Menses and Atrophy 149
Menses-related Changes (Figs. 7.1 and 7.5) 149
Atrophy-related Changes 149
References 149
Curettage-Related Changes (Figs. 7.2–7.4) 151
Epithelial Metaplasias 151
Syncytial Papillary Change (Fig. 7.5) 152
Squamous and Morular Metaplasia (Figs. 7.6–7.7 and 7.19) 152
Mucinous (including Intestinal) Metaplasia (Fig. 7.8) 153
Ciliated (Tubal) Metaplasia (Figs. 7.9–7.10) 154
Eosinophilic and Oncocytic Metaplasia (Fig. 7.11) 154
Hobnail Cell Metaplasia 155
Clear Cell Metaplasia (Fig. 7.12) 155
Mesonephric-like Metaplasia 155
References 155
General 155
Syncytial papillary change 155
Squamous and morular metaplasia 155
Mucinous and intestinal metaplasia 156
Other types 156
Pregnancy-Related and Hormonal Changes 156
Arias-Stella Reaction (Fig. 7.13) 156
Clear Cell Change 156
Optically Clear Nuclei (Fig. 7.14) 156
Decidua (Figs. 7.15–7.16) 157
Effects of Exogenous Hormones (Figs. 7.17–7.20) 157
Heterotopic Tissues (Fig. 7.21) 159
References 159
Inflammatory and Reparative Lesions 160
Chronic Endometritis (Figs. 7.22–7.24) 160
Microscopic findings 160
Clinicopathologic correlation and differential diagnosis 161
Focal Necrotizing Endometritis (Fig. 7.25) 161
Florid Reactive Lymphoid Hyperplasia (Lymphoma-like Lesion) (Fig. 7.26) 161
Granulomatous Endometritis, including Effects of Thermal Ablation (Figs. 7.27–7.28) 162
Xanthogranulomatous Endometritis and Myometrial Xanthomatosis (Fig. 7.29) 162
Malacoplakia (Fig. 7.30) 163
Histiocytic Nodules (Fig. 7.31) 163
Eosinophilic Infiltrates 164
Mast Cell Infiltrates 164
Ligneous Endometritis 164
Pneumopolycystic Endometritis 164
Postoperative Spindle Cell Nodule 164
Intrauterine Device-related Changes, including Actinomycosis (Figs. 7.32–7.33) 164
Radiation-induced Changes (Fig. 7.34) 165
Arteritis 165
Viral Lesions 165
References 165
Chronic endometritis 165
Focal necrotizing endometritis 166
Florid reactive lymphoid hyperplasia (lymphoma-like lesion) 166
Granulomatous endometritis, including effects of thermal ablation 166
Xanthogranulomatous endometritis and myometrial xanthomatosis 166
Malacoplakia 166
Histiocytic nodules 166
Eosinophilic infiltrates 166
Mast cell infiltrates 166
Ligneous endometritis 166
Pneumopolycystic endometritis 166
Postoperative spindle cell nodule 166
Intrauterine device-related changes, including actinomycosis 166
Radiation-induced changes 166
Viral infections 166
Endometrial Polyps (Figs. 7.35–7.40, 7.46) 167
Clinical and gross features 167
Microscopic features 168
Differential diagnosis 169
7 Abstracts and Keywords e7
Abstract: e7
Keywords: e7
8 Endometrial Hyperplasia and Carcinoma 176
Endometrial Hyperplasia 176
Classification 176
Clinical features 177
Pathological features (Figs. 8.1–8.4) 177
Behavior 178
Differential diagnosis (Fig. 8.5) 179
References 180
General 180
Immunohistochemistry, molecular findings, and EIN 180
Endometrial Carcinoma 181
Classification 181
Gross features (Fig. 8.6) 181
Endometrioid Carcinoma, Usual Type 181
Clinical and general features 181
Typical microscopic features (Figs. 8.7–8.12) 182
Squamous differentiation (Figs. 8.13–8.15) 183
Unusual patterns including microglandular, sertoliform, and CHEC (Figs. 8.16–8.18) 185
Unusual cell types including ciliated, oxyphilic, clear, and spindle (Figs. 8.19–8.22) 186
Patterns of myometrial invasion (Figs. 8.23–8.28) 186
Findings often over-interpreted as myometrial invasion (Fig. 8.29–8.30) 189
Grading 190
Patterns of cervical involvement (Fig. 8.31) 190
Carcinomas arising in unusual locations 191
Carcinomas related to Lynch syndrome and other disorders with mismatch repair protein defects (Fig. 8.32) 192
Effects of treatment 192
Immunohistochemical and molecular findings 193
Markers helpful in distinction from endocervical adenocarcinoma 193
Markers helpful in the distinction from serous carcinomas (see corresponding heading) 193
Markers of potential prognostic and therapeutic significance 193
Findings in recurrences 194
Differential diagnosis 194
Prognostic factors 194
Endometrioid Carcinoma, Unusual Types 195
Secretory Carcinoma (Figs. 8.33–8.34) 195
Villoglandular Endometrioid Carcinoma (Figs. 8.35–8.36) 196
Endometrioid Carcinoma with Small Nonvillous Papillae (Fig. 8.37) 197
Ciliated Carcinoma 197
Serous Carcinoma 197
Clinical features 197
Pathological features (Figs. 8.38–8.46) 198
Immunohistochemical findings 200
Molecular findings 200
Behavior and prognostic factors 201
Differential diagnosis (Table 8.3) 201
Clear Cell Carcinoma 202
Clinical features 202
Pathologic features (Figs. 8.47–8.48) 202
Behavior and prognostic features 203
Differential diagnosis (Table 8.4) 203
Mucinous carcinoma 203
Clinical features 203
Pathologic features (Figs. 8.49–8.51) 204
Behavior 204
Differential diagnosis 204
Squamous Cell Carcinoma 205
Clinical features 205
Criteria for diagnosis 205
Pathological features (Figs. 8.52–8.53) 205
8 Abstracts and Keywords e8
Abstract: e8
Keywords: e8
9 Mesenchymal and Mixed Epithelial–Mesenchymal Tumors of the Uterine Corpus and Cervix 218
Smooth Muscle Tumors 219
Leiomyoma, Usual Type 219
Clinical features 219
Usual gross features (Fig. 9.1) 219
Usual microscopic features (Figs. 9.2–9.5) 219
Hormonal and pregnancy-related changes 221
Changes secondary to uterine artery embolization and antifibrinolytic agents (Fig. 9.6) 221
Leiomyoma Variants 221
Cellular Leiomyoma and Highly Cellular Leiomyoma (Figs. 9.7–9.10) 221
Leiomyomas with Bizarre Nuclei (LBNs) (Figs. 9.11–9.12) 223
Mitotically Active Leiomyoma 224
Hydropic Leiomyoma (Figs. 9.13–9.16) 224
Myxoid Leiomyoma (Fig. 9.17) 225
Apoplectic Leiomyoma (Fig. 9.18) 226
Leiomyomas with Rare Findings (Fig. 9.19) 226
Leiomyosarcoma 227
Leiomyosarcoma of Usual Type 227
Clinical features 227
Gross features (Fig. 9.20) 227
Typical microscopic features (Figs. 9.21–9.22) 227
Rare microscopic features 229
Immunohistochemical and molecular features 229
Behavior and prognosis 229
Differential diagnosis 230
Myxoid Leiomyosarcoma (Figs. 9.23–9.25) 230
Epithelioid Leiomyosarcoma (see Epithelioid Smooth Muscle Tumors) 231
Smooth Muscle Tumors of Uncertain Malignant Potential 231
Epithelioid Smooth Muscle Tumors 232
General features 232
Pathological features (Figs. 9.26–9.30) 232
Criteria for epithelioid leiomyosarcoma and its behavior 233
Differential diagnosis 233
Tumors of Perivascular Epithelioid Cell Origin 233
Perivascular Epithelioid Cell Tumors of Usual Type (PEComas) (Figs. 9.31–9.32) 233
Differential diagnosis 235
Angiomyolipoma 235
Lymphangioleiomyomatosis (Fig. 9.33) 235
Benign-Appearing Smooth Muscle Tumors with Unusual Growth Patterns or Behavior 235
Low-grade Smooth Muscle Tumor of Probable Multicentric Origin 235
Diffuse Uterine Leiomyomatosis 236
Dissecting Leiomyoma, including the Cotyledonoid Variant (Fig. 9.34) 236
Leiomyoma with Vascular Invasion 237
Intravenous Leiomyomatosis 237
Clinical features 237
Pathological features (Figs. 9.35–9.37) 237
Differential diagnosis (Fig. 9.38) 237
Behavior 238
Benign Metastasizing Leiomyoma (Fig. 9.39) 239
‘Parasitic’ Leiomyoma 239
Disseminated Peritoneal Leiomyomatosis (see Chapter 19) 239
References 239
Leiomyomas: general features 239
Leiomyomas: treatment-related findings 239
Cellular leiomyoma and highly cellular leiomyoma 240
Leiomyomas with bizarre nuclei (LBNs) 240
Mitotically active leiomyoma 240
Hydropic leiomyoma 240
Myxoid leiomyoma 240
Apoplectic leiomyoma 240
Leiomyomas with rare findings 240
Leiomyosarcoma: usual findings 241
Leiomyosarcoma: immunohistochemical and molecular findings 241
Leiomyosarcoma: unusual findings 241
Myxoid leiomyosarcoma 241
Smooth muscle tumors of uncertain malignant potential 241
Epithelioid smooth muscle tumors 242
Perivascular epithelioid cell tumors 242
Low-grade smooth muscle tumors of probable multicentric origin 242
Diffuse uterine leiomyomatosis 242
Dissecting leiomyoma, including the cotyledonoid variant 242
Leiomyoma with vascular invasion 242
Intravenous leiomyomatoisis 242
Benign metastasizing leiomyoma 243
‘Parasitic’ leiomyoma 243
Endometrial Stromal and Related Tumors 243
Endometrial Stromal Nodule and Endometrial Stromal Tumor with Limited Infiltration 243
Clinical and usual pathological features (Figs. 9.40–9.43) 243
Differential diagnosis 244
Low-Grade Endometrial Stromal Sarcoma 245
Clinical features 245
Usual pathological features (Figs. 9.44–9.48) 245
Usual immunohistochemical findings 245
Cytogenetic findings 246
Unusual pathological features of endometrial stromal tumors (Figs. 9.49–9.60) 246
Fibrous and myxoid change 246
Smooth muscle differentiation 248
Sex-cord-like elements 249
Glands 249
Papillae and pseudopapillae 249
Epithelioid cells 249
Associated high-grade component 249
YWHAE-FAM22 ESSs 250
Other Rare Findings 250
Differential diagnosis 250
Behavior and prognostic features 250
Undifferentiated Endometrial Sarcoma (Fig. 9.61) 251
Differential diagnosis 251
Endocervical Stromal Sarcoma 252
References 252
Endometrial stromal nodule and endometrial stromal tumor with limited infiltration 252
Endometrial stromal sarcomas: general features 252
Endometrial stromal sarcomas: usual immunohistochemical and molecular findings 252
Endometrial stromal tumors with unusual features 252
Undifferentiated endometrial sarcoma 253
Endocervical stromal sarcoma 253
Mixed Epithelial and Mesenchymal Tumors 253
Malignant Müllerian Mixed Tumor 253
Nomenclature and histogenesis 253
Clinical features 253
Gross appearance (Fig. 9.62) 254
Microscopic appearance (Figs. 9.63–9.64) 254
Immunohistochemical and molecular findings 255
Differential diagnosis 255
Behavior and prognostic factors 255
Müllerian Adenofibroma (Fig. 9.65) 255
Müllerian Adenosarcoma 256
Typical 256
Clinical features 256
Gross appearance (Fig. 9.66) 256
Microscopic appearance (Figs. 9.67–9.71) 256
Differential diagnosis 258
Behavior 259
With Sarcomatous Overgrowth (Fig. 9.72) 259
Müllerian Carcinofibroma and Carcinomesenchymoma 259
Adenomyomas 259
Of Endocervical Type (see Chapter 4) 259
Of Typical Endometrioid Type (Figs. 9.73–9.74) 259
Atypical Polypoid Adenomyoma 260
Clinical and gross findings (Fig. 9.75) 260
Microscopic findings (Figs. 9.76–9.77) 261
Differential diagnosis 262
Behavior 262
Uterine Tumors Resembling Ovarian Sex-Cord Tumors 262
Clinical features 262
Pathological features (Figs. 9.78–9.83) 262
Differential diagnosis 264
Behavior 264
References 264
MMMTs: usual features 264
MMMTs: unusual pathologic features 264
MMMTs: immunohistochemistry and molecular studies 265
Müllerian adenofibroma 265
Müllerian adenosarcoma 265
Müllerian carcinofibroma and carcinomesenchymoma 265
Adenomyoma of typical endometrioid type 265
Atypical polypoid adenomyoma 266
Uterine tumors resembling ovarian sex-cord tumors 266
Rare Sarcomas 266
Homologous Sarcomas 266
Vascular Tumors 266
Malignant Fibrous Histiocytoma and Giant Cell Tumors 266
Malignant Peripheral Nerve Sheath Tumors (Fig. 9.84) 267
Heterologous Sarcomas 267
Embryonal Rhabdomyosarcoma (including Sarcoma Botryoides) (Figs. 9.85–9.86) 267
Differential diagnosis 268
Rare Heterologous Sarcomas 268
Extragastrointestinal Stromal Tumors 268
Sarcomas of Uncertain Histogenesis 268
Alveolar Soft Part Sarcoma 268
Malignant Rhabdoid Tumor 268
Epithelioid Sarcoma 268
References 269
Vascular tumors 269
Malignant fibrous histiocytoma and giant cell tumors 269
Malignant peripheral nerve sheath tumors 269
Embryonal rhabdomyosarcoma 269
Rare heterologous sarcomas 269
Extragastrointestinal stromal tumors 269
Alveolar soft part sarcoma 269
Malignant rhabdoid tumor 269
Epithelioid sarcoma 269
Benign Mesenchymal Tumors of Soft Tissue Type 270
Inflammatory Myofibroblastic Tumor (Fig. 9.87) 270
Others 270
References 270
Inflammatory myofibroblastic tumor 270
Other benign mesenchymal tumors of soft tissue type 270
Acknowledgment 270
9 Abstracts and Keywords e9
Abstract: e9
Keywords: e9
10 Trophoblastic Lesions, Miscellaneous Primary Uterine Neoplasms, Hematopoietic Neoplasms, and Metastatic Neoplasms to the Uterus 271
Trophoblastic Lesions 272
Hydatidiform Moles 272
Complete Hydatidiform Mole 272
Clinical and cytogenetic features 272
Pathological features (Figs.10.2–10.5) 273
Differential diagnosis 274
Behavior 275
Partial Hydatidiform Mole 276
Clinical and cytogenetic features 276
Pathological features (Figs.10.6–10.7) 276
Differential diagnosis 277
Behavior 277
Hydropic Abortus (Fig. 10.8) 277
Choriocarcinoma 278
Clinical features 278
Pathological features (Figs. 10.9–10.10) 278
Differential diagnosis 279
Behavior 279
Lesions of Intermediate Trophoblast 279
Normal Intermediate Trophoblast (Fig. 10.11) 279
Exaggerated Placental Site (Figs. 10.12–10.13) 280
Placental Site Nodules and Plaques 280
Clinical findings 280
Pathological findings (Figs. 10.14–10.17) 281
Differential diagnosis 281
Placental Site Trophoblastic Tumor (Figs. 10.18–10.20) 282
Clinical features 282
Gross features 283
Microscopic and molecular features 283
Differential diagnosis 283
Behavior 284
Epithelioid Trophoblastic Tumor (Figs. 10.21–10.22) 284
Differential diagnosis 284
Tumor-Like Abnormalities of Placentation 285
Placental Polyps (Fig. 10.23) 285
Placenta Accreta, Increta, and Percreta 285
References 285
Hydatidiform moles 285
Choriocarcinoma 286
Exaggerated placental site 286
Placental site nodule 286
Placental site trophoblastic tumor 286
Epithelioid trophoblastic tumor 286
Placenta accreta, increta, and percreta 287
Miscellaneous Primary Tumors 287
Adenomatoid Tumor 287
General features 287
Pathological features (Figs. 10.24–10.26) 287
Differential diagnosis 288
Germ Cell Tumors 288
Yolk Sac Tumor 288
Teratomas 288
Neuroectodermal Tumors 289
Primitive Neuroectodermal Tumor (PNETs) 289
Differential diagnosis 289
Pigmented Neuroectodermal Tumor of Infancy 289
Uterine Glioma 289
Other Neuroectodermal Tumors 289
Wilms’ Tumor 289
Malignant Melanoma 290
Clinical features 290
Pathological findings 290
Differential diagnosis 290
Brenner Tumor 290
References 290
Adenomatoid tumor 290
Yolk sac tumor 290
Teratomas 290
Primitive neuroectodermal tumor 290
Pigmented neuroectodermal tumor of infancy 291
Uterine glioma 291
Other neuroectodermal tumors 291
Wilms’ tumor 291
Malignant melanoma 291
Brenner tumor 291
HematopoIetic and Histiocytic Disorders 291
Lymphoma 291
Lymphoma Presenting in the Uterus (Figs. 10.27–10.30) 291
Clinical features 291
Gross features 292
Microscopic features 292
Differential diagnosis 292
Behavior 293
Uterine Involvement in Patients with Disseminated Lymphoma 293
Uterine Involvement by Leukemia (Fig. 10.31) 293
Leukemia Presenting in the Uterus 293
Uterine Involvement in Patients with Recognized Leukemia 294
Plasmacytoma 294
Uterine Involvement by Histiocytic Disorders (Figs. 10.32–10.33) 294
References 294
Uterine involvement by lymphoma 294
Uterine involvement by leukemia 295
Plasmacytoma 295
Uterine involvement by histiocytic disorders 295
Metastatic Carcinomas to the Uterus 295
From Genital Tract Carcinomas 295
From Extragenital Carcinomas (Figs. 10.34–10.36) 295
References 297
10 Abstracts and Keywords e10
Abstract: e10
Keywords: e10
11 The Fallopian Tube and Broad Ligament 298
Tumor-Like Lesions of the Fallopian Tube 299
Inflammatory Lesions 299
Usual Bacterial Salpingitis (Figs. 11.1–11.5) 299
Actinomycotic Salpingitis 300
Tuberculous Salpingitis (Fig. 11.6) 300
Other Causes of Granulomatous and Histiocytic Salpingitis (Figs. 11.7–11.10) 300
Ligneous Salpingitis 301
Arteritis (Fig. 11.11) 301
Epithelial Hyperplasia 301
Usual Type (Figs. 11.12–11.13) 301
Differential diagnosis 301
Papillary Tubal Hyperplasia including Secretory Cell Outgrowths (SCOUTs) (Fig. 11.14) 302
Pregnancy-Related CHANGES 302
Ectopic Pregnancy (Figs. 11.15–11.16) 302
Hydatidiform Mole 303
Placental Site Nodule 303
Arias-Stella Reaction (Fig. 11.17) 303
Clear Cell Change of Pregnancy 303
Ectopic Decidua (Fig. 11.18) 303
Metaplasias and Ectopias 303
Endometriosis (Fig. 11.19) 303
Mucinous Metaplasia (Fig. 11.20) 304
Transitional Cell and Squamous Metaplasia (Fig. 11.21) 304
Metaplastic Papillary ‘Tumor’ (Fig. 11.22) 305
Rare Ectopic Tissues (Figs. 11.23–11.24) 305
Miscellaneous Tumor-Like Lesions 305
Salpingitis Isthmica Nodosa (Fig. 11.25) 305
Torsion 306
Microcalcification 306
Artifacts (Figs. 11.26–11.27) 306
Prolapse (see Chapter 3) 306
References 306
Salpingitis: general features 306
Ligneous salpingitis 306
Arteritis 306
Epithelial hyperplasia: usual type 306
Papillary tubal hyperplasia including secretory cell outgrowths (SCOUTs) 307
Ectopic pregnancy 307
Hydatidiform mole 307
Placental site nodule 307
Arias-Stella reaction 307
Clear cell change of pregnancy 307
Ectopic decidua 307
Endometriosis 307
Mucinous metaplasia 307
Transitional cell and squamous metaplasia 307
Metaplastic papillary ‘tumor’ 307
Rare ectopic tissues 307
Salpingitis isthmica nodosa 307
Torsion 307
Microcalcification 307
Artifacts 307
Tumors of the Fallopian Tube 308
Benign and Borderline Epithelial Tumors 308
Endometrioid Polyp 308
Papilloma, Adenoma, and Cystadenoma 308
Adenofibroma and Cystadenofibroma (Fig. 11.28) 308
Borderline Tumors 308
Carcinomas 308
General and Pathologic Features 308
Clinical features 308
Gross features (Fig. 11.29) 309
Microscopic features (Figs. 11.30–11.34) 309
Differential diagnosis 311
Behavior 311
BRCA-related Tubal Carcinomas and Precursor Lesions (Figs. 11.35–11.36) 311
Serous tubal intraepithelial carcinoma (STIC) 312
Potential precursors of STIC (Fig. 11.37) 313
Differential diagnosis of STIC 314
Malignant Mixed Epithelial–Mesenchymal Tumors 314
Malignant Müllerian Mixed Tumors (MMMTs) 314
Adenosarcoma 314
Pure Mesenchymal Tumors 314
Benign Tumors 314
Sarcomas 314
Adenomatoid Tumor 315
General features 315
Pathological features (Fig. 11.38) 315
Differential diagnosis 315
Germ Cell Tumors 315
Trophoblastic Tumors 315
Choriocarcinoma 315
Placental Site Trophoblastic Tumor and Epithelioid Trophoblastic Tumor 315
Malignant Lymphoma and Leukemia 315
Secondary Tumors 315
From Other Female Genital Tract Sites (Fig. 11.39) 315
From Extragenital Sites 316
References 316
Benign and borderline epithelial tumors 316
Carcinomas: general and pathologic features 316
BRCA-related carcinomas and precursor lesions 316
Malignant müllerian mixed tumors (MMMTs) 317
Adenosarcoma 317
Benign mesenchymal tumors 317
Sarcomas 317
Adenomatoid tumors 317
Germ cell tumors 318
Choriocarcinoma 318
Placental site trophoblastic tumor and epithelioid trophoblastic tumor 318
Malignant lymphoma and leukemia 318
Metastatic tumors 318
Tumor-Like Lesions of the Broad Ligament 318
Embryonic Rests (Figs. 11.40–11.41) 318
Cysts (Fig.11.42) 318
Other Tumor-Like Lesions 319
References 319
Tumors of the Broad Ligament 319
Epithelial Tumors of Müllerian Type (Fig. 11.43) 319
Epithelial Tumors of Definite or Probable Wolffian Origin 319
Papillary Cystadenoma 319
Female Adnexal Tumor of Probable Wolffian Origin (Fig. 11.44) 320
Ependymoma and Primitive Neuroectodermal Tumors 320
Mixed Epithelial–Mesenchymal Tumors (Fig. 11.45) 321
Soft Tissue Tumors 321
Benign 321
Malignant 321
Miscellaneous and Secondary Tumors 321
References 321
Epithelial tumors of müllerian type 321
Papillary cystadenoma 322
Female adnexal tumor of probable wolffian origin 322
Ependymoma and primitive neuroectodermal tumors 322
Mixed epithelial–mesenchymal tumors 322
Benign soft tissue tumors 322
Malignant soft tissue tumors 322
Miscellaneous and secondary tumors 322
11 Abstracts and Keywords e11
Abstract: e11
Keywords: e11
12 Tumor-like Lesions of the Ovary 323
Follicular and Stromal Lesions 324
Follicle Cyst 324
Clinical features 324
Pathological features (Figs. 12.1–12.3) 324
Differential diagnosis with unilocular granulosa cell tumor 324
Corpus Luteum Cyst (Figs. 12.4–12.5) 325
Polycystic Ovarian Syndrome (Stein–Leventhal Syndrome) 325
Clinical features 325
Pathological features (Figs. 12.6–12.8) 325
Differential diagnosis 326
Stromal Hyperthecosis 326
Clinical features 326
Pathological features (Figs. 12.9–12.11) 326
12 Abstracts and Keywords e12
Abstract: e12
Keywords: e12
13 Surface Epithelial–Stromal Tumors: 343
General Features of Surface Epithelial–Stromal Tumors 343
Classification 343
Grading of Ovarian Carcinomas 344
Clinical Features and Prognostic Factors 344
Hereditary Ovarian Cancer 345
BRCA-related Ovarian Carcinomas 345
HNPPC-related Ovarian Carcinomas 345
References 346
Grading 346
Hereditary ovarian cancer 346
Serous Tumors 346
Benign Serous Tumors 346
Gross features (Figs. 13.1–13.2) 346
Microscopic features (Figs. 13.3–13.4) 346
Differential diagnosis 347
Borderline Serous Tumors 347
Gross features (Fig. 13.5) 348
Usual microscopic features of primary tumors (Figs. 13.6–13.9) 348
Unusual microscopic features of primary tumors (Figs. 13.10–13.17) 349
Microscopic features of implants of serous borderline tumors (Figs. 13.18–13.22) 352
Immunohistochemical and molecular findings 354
Lymph node involvement by serous borderline tumor (Figs. 13.23–13.24) 354
Lymph node involvement by low-grade serous carcinoma in patients with serous borderline tumors 355
Differential diagnosis 355
Prognostic factors in serous borderline tumors 356
Operative findings 356
Features of primary tumors 356
Features of implants, metastases, and recurrences 356
High-grade Serous Carcinomas 357
Clinical features 357
Gross features (Fig. 13.25–13.26) 357
Microscopic features of usual high-grade serous carcinomas (Figs. 13.27–13.34) 358
Microscopic features of BRCA-related high-grade serous carcinomas 360
Immunohistochemistry and molecular findings of low- and high-grade serous carcinomas 360
Differential diagnosis 360
Behavior and prognostic factors 361
Low-grade Serous Carcinomas (Figs. 13.35–13.40) 362
Clinical features 362
Pathological features 362
Behavior 363
References 363
Serous borderline tumors: general features 363
Serous borderline tumors: unusual features, including micropapillary tumors, microinvasion, autoimplants, lymph node involvement, and associated high-grade component 364
High-grade serous carcinoma: general and histological features 365
Serous carcinomas: immunohistochemical and molecular findings 365
Low-grade serous carcinomas 366
Mucinous Tumors 366
General features and histogenesis 366
Clinical features 367
Intestinal-type Mucinous Tumors of Usual Type 367
Gross features (and sampling) of intestinal-type mucinous tumors (Figs. 13.41–13.43) 367
Microscopic features of benign tumors of intestinal type (Figs. 13.44–13.46) 368
Microscopic features of intestinal mucinous borderline tumors (usual type, with intraepithelial carcinoma, and with microinvasion) (Figs. 13.47–13.55) 369
Microscopic features of intestinal-type mucinous carcinomas (Figs. 13.56–13.59) 371
Immunohistochemical and molecular findings in intestinal-type mucinous tumors 372
Differential diagnosis of intestinal-type mucinous tumors 373
Behavior and prognosis of intestinal-type mucinous tumors 373
Teratoma-associated Mucinous Tumors (Fig. 13.60) 374
Endocervical-like Mucinous Borderline Tumors (Figs. 13.61–13.64) 374
Differential diagnosis 376
Endocervical-like Mucinous Carcinomas 376
Mural Nodules in Mucinous Tumors (Figs. 13.65–13.66) 376
References 377
Mucinous tumors: general features 377
Mucinous tumors: immunohistochemistry and molecular findings 378
Teratoma-associated mucinous tumors 378
Endocervical-like mucinous borderline tumors 378
Endocervical-like mucinous carcinomas 378
Mural nodules in mucinous tumors 378
13 Abstracts and Keywords e13
Abstract: e13
Keywords: e13
14 Surface Epithelial–Stromal Tumors: 380
Endometrioid Epithelial Tumors 380
General features 380
Gross features (Fig. 14.1) 381
Microscopic features of benign tumors (Figs. 14.2–14.4) 381
Microscopic features and behavior of borderline endometrioid tumors (Fig. 14.5) 382
Typical microscopic features of endometrioid carcinomas (Figs. 14.6–14.10) 382
Uncommon findings (Figs. 14.11–14.15) 384
Immunohistochemical and molecular findings 385
Differential diagnosis 385
Behavior 387
References 387
Endometrioid carcinomas: general features 387
Endometrioid carcinomas: unusual findings and subtypes 387
Synchronous uterine and ovarian endometrioid carcinomas 388
Malignant Mesodermal Mixed Tumor 388
General and gross features 388
Microscopic features (Fig. 14.16) 388
Differential diagnosis 388
Spread and prognosis 389
References 389
Adenosarcoma (Figs. 14.17–14.19) 389
Clinical and pathological features 389
Differential diagnosis 390
Spread and prognosis 390
References 390
Endometrioid Stromal Sarcoma 390
General features 390
Pathological features (Fig. 14.20) 390
Differential diagnosis 391
Spread and prognosis 391
References 391
Clear Cell Tumors 392
General features 392
Gross features (Fig. 14.21) 392
Microscopic features of benign and borderline clear cell tumors (Figs. 14.22–14.23) 392
Microscopic features of clear cell carcinomas (Figs. 14.24–14.30) 393
Immunohistochemical and molecular findings in clear cell carcinomas 395
Differential diagnosis 395
Behavior and prognostic factors 396
References 397
Clear cell carcinomas: morphologic, immunohistochemical, and molecular findings 397
Clear cell carcinomas: clinical and prognostic features, including grading 397
Transitional Cell Tumors (Figs. 14.31–14.39) 398
General features 398
Gross features of benign Brenner tumor (Fig. 14.31) 399
Gross features of other transitional cell tumors (Fig. 14.34) 400
Microscopic features of benign Brenner tumor (Figs. 14.32–14.33) 400
Microscopic features of borderline Brenner tumor (Fig. 14.35) 400
Microscopic features of malignant Brenner tumor (Fig. 14.36) 400
Microscopic features of transitional cell carcinoma (Figs. 14.37–14.39) 400
Immunohistochemical and molecular findings 400
Differential diagnosis 401
Spread and prognosis 401
References 401
Squamous Cell Tumors 402
14 Abstracts and Keywords e14
Abstract: e14
Keywords: e14
15 Germ Cell Tumors of the Ovary 408
General Features 408
Primitive Germ Cell Tumors (Nonteratomatous) 409
Dysgerminoma 409
Clinical features 409
Gross pathological findings (Fig. 15.1) 409
Microscopic findings (Figs. 15.2–15.8) 409
Differential diagnosis 411
Prognosis 412
Yolk Sac Tumor 412
Clinical features 412
Gross features (Figs. 15.9–15.10) 412
Typical microscopic features (Figs. 15.11–15.15) 412
Microscopic features of variant patterns (Figs. 15.16–15.20) 414
Polyvesicular vitelline 414
Hepatoid 415
Glandular 415
Differential diagnosis 415
Prognosis 415
Embryonal Carcinoma 415
Clinical features 415
Pathological features (Figs. 15.21–15.22) 416
Differential diagnosis 416
Prognosis 416
Polyembryoma (Figs. 15.23–15.24) 416
Nongestational Choriocarcinoma (Figs. 15.25–15.26) 417
Differential diagnosis 418
Prognosis 418
Mixed Primitive Germ Cell Tumors 418
References 418
Dysgerminoma 418
Yolk sac tumor 418
Embryonal carcinoma 419
Polyembryoma 419
Choriocarcinoma 419
Mixed primitive germ cell tumors 419
Teratomas (other than Monodermal) 419
Dermoid Cyst (Mature Cystic Teratoma) 419
Clinical features 419
Gross pathological features (Figs. 15.27–15.28) 419
Microscopic pathological features (Figs.15.29–15.33) 420
Differential diagnosis 420
Mature Solid Teratoma 421
Fetiform Teratoma (Homunculus) 422
Immature Teratoma 422
Clinical features 422
Pathological features (Figs. 15.34–15.38) 422
Differential diagnosis 423
Prognosis 424
References 424
Mature cystic teratoma (dermoid cyst) 424
Mature solid teratoma 424
Fetiform teratoma (homunculus) 424
Immature teratoma 424
Monodermal Teratomas 425
Struma Ovarii 425
Clinical features 425
Pathological features (Figs. 15.39–15.47) 425
Differential diagnosis 427
Struma-derived Carcinomas (Figs. 15.48–15.49) 427
Insular Carcinoid 428
Clinical features 428
Pathological features (Figs. 15.50–15.52) 428
Differential diagnosis 429
Behavior 429
Trabecular Carcinoid 429
Clinical features and behavior 429
Pathological features 430
Differential diagnosis 430
Strumal Carcinoid 430
Clinical features and behavior 430
Pathological features (Figs. 15.53–15.54) 430
15 Abstracts and Keywords e15
Abstract: e15
Keywords: e15
16 Sex Cord−Stromal and Steroid Cell Tumors of the Ovary 439
Sex Cord−Stromal Tumors 439
Granulosa Cell Tumors 439
Adult Granulosa Cell Tumor 439
General features 439
Gross features (Fig. 16.1) 440
Typical microscopic features (Figs. 16.2–16.6) 440
Uncommon or rare features (Fig. 16.7) 440
Immunohistochemical and molecular findings 442
Differential diagnosis 442
Behavior 444
Prognostic factors 444
Juvenile Granulosa Cell Tumor 445
General features 445
Pathologic features (Figs. 16.8–16.13) 445
Differential diagnosis 446
Behavior 447
Tumors in the Fibroma–Thecoma Group 447
Fibroma and Cellular Fibroma 447
Clinical features 447
Gross features (Fig. 16.14) 447
Microscopic features (Figs. 16.15–16.19) 447
16 Abstracts and Keywords e16
Abstract: e16
Keywords: e16
17 Miscellaneous Primary Ovarian Tumors 470
Small Cell Carcinoma of Hypercalcemic Type 470
Clinical features 470
Gross and microscopic features (Figs. 17.1–17.7) 471
Immunohistochemical, ultrastructural, and flow cytometric findings 472
Differential diagnosis (Table 17.1) 472
Behavior and prognosis 473
References 473
Tumors of Probable Wolffian Origin 473
Clinical features 473
Pathological findings 474
Differential diagnosis 474
Prognosis 474
References 474
Tumors of the Rete 474
Clinical features 474
Pathological findings (Fig. 17.8) 474
17 Abstracts and Keywords e17
Abstract: e17
Keywords: e17
18 Metastatic Tumors of the Ovary (including Pseudomyxoma Peritonei, Hematolymphoid Neoplasms, and Tumors with Functioning Stroma) 482
General Features (Figs. 18.1–18.8) 483
18 Abstracts and Keywords e18
Abstract: e18
Keywords: e18
19 Endometriosis and Lesions of the Secondary Müllerian System 513
References 514
Endometriosis 514
Clinical features 514
Gross findings (Figs. 19.1–19.3) 514
Typical microscopic findings (Figs. 19.4–19.14) 515
Microscopic findings causing diagnostic problems including underdiagnosis (Figs. 19.15–19.28) 518
Differential diagnosis 522
Atypical endometriosis and endometriosis-associated tumors (Figs. 19.29–19.30) 522
References 524
General 524
Atypical endometriosis and endometriosis-related tumors 524
Peritoneal endometrioid tumors unrelated to endometriosis 525
Peritoneal Serous Lesions 525
Endosalpingiosis (Fig. 19.31) 525
Clinical features 525
Pathologic findings 526
Differential diagnosis 526
Peritoneal Serous Borderline Tumors (Figs. 19.32–19.33) 526
Clinical features 527
Pathological features 527
Behavior 527
Low-grade Peritoneal Serous Carcinomas, including Psammocarcinomas (Fig. 19.34) 527
High-grade Peritoneal Serous Carcinomas 528
Differential diagnosis 528
References 528
Endosalpingiosis 528
Peritoneal serous borderline tumors 529
Low-grade peritoneal serous carcinomas, including psammocarcinomas 529
High-grade peritoneal serous carcinomas 529
Peritoneal Mucinous Lesions 529
Endocervicosis (including Müllerianosis) (Figs. 19.35–19.36) 529
Differential diagnosis 529
Retroperitoneal Mucinous Tumors (Figs. 19.37–19.38) 530
References 530
Endocervicosis 530
Retroperitoneal mucinous tumors 531
Peritoneal Transitional, Squamous, Clear Cell, and Other Rare Lesions (Figs. 19.39–19.41) 531
References 531
Subperitoneal Mesenchymal Lesions 532
Peritoneal Decidual Reaction 532
Clinical and operative findings 532
Microscopic findings (Figs. 19.42–19.43) 532
Disseminated Peritoneal Leiomyomatosis 532
Clinical findings 532
Pathological features (Figs. 19.44–19.46) 533
Behavior 533
Histogenesis 533
References 533
Ectopic decidua 533
Disseminated peritoneal leiomyomatosis 533
Retroperitoneal Lymph Node Lesions 534
Benign Glands of Müllerian Type 534
Clinical features 534
Pathologic findings (Figs. 19.47–19.48) 534
Differential diagnosis 535
Primary Intranodal Serous Borderline Tumors and Low-grade Serous Carcinoma (see Chapter 13) 535
Decidua (Fig. 19.49) 535
Leiomyomatosis (Fig. 19.50) 535
19 Abstracts and Keywords e19
Abstract: e19
Keywords: e19
20 Tumor-like Lesions and Tumors of the Peritoneum (Excluding Müllerian Lesions) 537
Tumor-Like Lesions 537
Inflammatory and Reparative Lesions 537
Granulomatous Peritonitis (Figs. 20.1–20.4) 537
Nongranulomatous Histiocytic Lesions (Figs. 20.5–20.8) 538
Peritoneal Fibrosis (Figs. 20.9–20.10) 539
Mesothelial Lesions 541
Mesothelial Hyperplasia (Figs. 20.11–20.17) 541
Differential diagnosis 542
Peritoneal Inclusion Cysts (Figs. 20.18–20.22) 542
Unilocular PICs 542
Multilocular PICs 543
Miscellaneous Lesions 544
Splenosis (Fig. 20.23) 544
Trophoblastic Implants (Fig. 20.24) 544
Infarcted Appendix Epiploica (Fig. 20.25) 544
Other Tumor-like Lesions 545
References 545
Inflammatory and reparative lesions 545
Mesothelial hyperplasia 545
Multilocular PICs 546
Splenosis 546
Trophoblastic implants 546
Infarcted appendix epiploica 546
Other tumor-like lesions 546
Tumors 546
Mesotheliomas 546
Adenomatoid Tumor 546
Well-differentiated Papillary Mesothelioma (Fig. 20.26) 546
Malignant Mesothelioma 547
Clinical features 547
Typical pathological findings (Figs. 20.27–20.32) 547
Unusual histologic variants and findings (Figs. 20.28–20.34) 548
Differential diagnosis 549
Behavior and prognostic factors 550
Intra-Abdominal Desmoplastic Small Round-Cell Tumor 550
Clinical features 550
Pathological features (Figs. 20.35–20.37) 550
Immunohistochemical and ultrastructural features 551
Differential diagnosis 551
Mesenchymal Tumors 551
Solitary Fibrous Tumor 551
Inflammatory Myofibroblastic Tumor 551
Calcifying Fibrous Tumor 552
Omental–Mesenteric Myxoid Hamartoma 552
Sarcomas 552
Rare Primary Tumors 552
Metastatic Tumors (Figs. 20.38–20.39) 552
References 553
Well-differentiated papillary mesothelioma 553
Malignant mesothelioma: general features 553
Malignant mesothelioma: immunohistochemistry 553
Intra-abdominal desmoplastic small round cell tumor 554
Solitary fibrous tumor 554
Inflammatory myofibroblastic tumor 554
Calcifying fibrous tumor 554
Omental–mesenteric myxoid hamartoma 554
Sarcomas 554
Rare primary tumors 554
Metastatic tumors 554
20 Abstracts and Keywords e20
Abstract: e20
Keywords: e20
INDEX 555
A 555
B 556
C 556
D 557
E 557
F 559
G 559
H 560
I 560
J 560
K 560
L 560
M 561
N 562
O 562
P 563
R 564
S 564
T 566
U 566
V 567
W 568
X 568
Y 568
Z 568