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Enzinger and Weiss's Soft Tissue Tumors E-Book

Enzinger and Weiss's Soft Tissue Tumors E-Book

John R. Goldblum | Sharon W. Weiss | Andrew L. Folpe

(2013)

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Book Details

Abstract

Enzinger and Weiss's Soft Tissue Tumors is your essential medical reference on the diagnosis of tumors of the skeletal muscles, connective tissue, fat, and related structures. No other source matches Enzinger and Weiss’s scope and depth of coverage in this complex and challenging area of surgical pathology, and no other text contains as much practical information on differential diagnosis. Microscopic findings are correlated with the latest developments in molecular biology, cytogenetics, and immunohistochemistry, providing you with a comprehensive and integrated approach to the evaluation of soft tissue specimens.

  • Consult this title on your favorite e-reader, conduct rapid searches, and adjust font sizes for optimal readability.
  • Compare what you see under the microscope to nearly 2,000 superb images that capture the appearance of a complete range of pathological entities and help you relate their characteristics to their specific classifications.
  • Apply the latest knowledge on FNA biopsy, molecular biology, and cytogenetics.
  • Make rapid and effective decisions with the aid of extensive algorithms, and access information at a glance with abundant tables and graphs.
  • Take advantage of all of the essential clinical and prognostic data on soft tissue tumors that are necessary to formulate complete sign-out reports.
  • Navigate through the book quickly thanks to summary outlines at the beginning of each chapter, a color-coded page design, and a consistent approach to every entity.
  • Apply the latest advances in surgical pathology thanks to major updates on recently identified pathological entities such as soft tissue angiofibroma and CIC-related sarcomas; coverage of the newest molecular diagnostic techniques and immunohistochemical and molecular genetic features of soft tissue tumors; new chapters on GIST and soft tissue tumors showing melanocytic differentiation; and more.
  • Effortlessly find the information you need with a chapter organization based on the newest surgical pathology concepts and classifications of soft tissue tumors.

Table of Contents

Section Title Page Action Price
Front Cover cover
Inside Front Cover ifc1
Enzinger and Weiss's Soft Tissue Tumors, 6/e i
Copyright Page iv
Dedication v
Contributors vii
Preface to the Sixth Edition ix
Preface to the First Edition xi
Table Of Contents xiii
1 General Considerations 1
Chapter Contents 1
Incidence of Soft Tissue Tumors 1
Pathogenesis of Soft Tissue Tumors 1
Environmental Factors 2
Oncogenic Viruses 3
Immunologic Factors 3
Genetic Factors 3
Classification of Soft Tissue Tumors 3
Grading and Staging Soft Tissue Sarcomas 3
Grading Systems 3
Limitations of Grading 5
Staging Systems 6
AJCC Staging System 6
Musculoskeletal Tumor Society Staging System 7
Advantages and Disadvantages of Staging Systems 7
References 9
2 Clinical Evaluation and Treatment of Soft Tissue Tumors 11
Chapter Contents 11
Introduction 11
Clinical Evaluation 11
Clinical Presentation and Assessment 11
Pretreatment Evaluation 12
Biopsy 12
Staging 13
Prognostic Factors 14
Clinicopathologic Factors 14
Classification and Prognostic Significance of Surgical Margins 14
Nomograms for Assessment of Individual Patient Prognosis 14
Treatment of Localized Primary Extremity Sarcomas 15
Surgery 15
Combined Modality Limb-Sparing Treatment 16
Treatment by Surgery Alone—without Radiotherapy 16
Amputation 17
Management of Regional Lymph Nodes 17
Radiotherapy 17
Rationale for Combining Radiotherapy with Surgery 17
Sequencing of Radiotherapy and Surgery 17
Radiation Treatment Techniques 18
Chemotherapy 19
Chemotherapy Following Primary Surgical Resection 19
Adjuvant and Neoadjuvant Studies Since the 1997 Meta-Analysis 20
Preoperative (Neoadjuvant) Chemotherapy 20
Recent Analyses of Multicenter Data Regarding Adjuvant Therapy for STS 21
Treatment of Locally Advanced Disease 22
Hyperthermic Isolated Limb Perfusion 22
Radiation Alone 22
Management of Local Recurrence 22
Key Points 23
References 23
3 Radiologic Evaluation of Soft Tissue Tumors 25
Chapter Contents 25
Introduction 25
Imaging Modalities 25
Radiography 25
Ultrasonography 25
Computed Tomography 25
Positron Emission Tomography– Computed Tomography 26
Magnetic Resonance Imaging 26
Imaging Features of Common Benign Soft Tissue Tumors 26
Lipomas, Lipoma Variants, and Atypical Lipomatous Tumors/Well-Differentiated Liposarcomas 26
Benign Neurogenic Tumors 27
Benign Vascular Lesions 31
Low-Flow Vascular Malformations 32
High-Flow Vascular Malformations 33
Hemangiomas 34
Congenital Hemangioma 37
Desmoid Tumors 37
Myxomas 37
Uncommon Benign Soft Tissue Tumors 40
Desmoplastic Fibroblastomas 40
Leiomyomas 40
Glomus Tumors 41
Fibromas of Tendon Sheath 42
Myofibromas 43
Granular Cell Tumors 43
Soft Tissue Sarcomas 44
Uncommon Malignant Soft Tissue Tumors 52
Common Tumor-Like Conditions 54
Elastofibromas 54
Hematomas 57
Pigmented Villonodular Synovitis 58
Synovial Chondromatosis 59
Ganglia, Synovial Cysts, and Bursitis 60
Postoperative Collections 62
Abscesses 62
Heterotopic Ossification 62
Accessory or Hypertrophied Muscles 67
Uncommon Tumor-Like Conditions 67
Decubital Ischemic Fasciitis (Atypical Decubital Fibroplasia or Ischemic Fasciitis) 67
Nodular Fasciitis 71
Lipomatosis of Nerves 72
Subcutaneous Granuloma Annulare 72
References 74
4 Cytogenetic and Molecular Genetic Pathology of Soft Tissue Tumors 76
Chapter Contents 76
Introduction 76
General Concepts in Cancer Genetics 76
General Principles of Translocations 77
Diagnostic Methods 80
Chromosome, Fluorescence In Situ Hybridization, and Gene Nomenclature 80
Methodologic Considerations 81
Molecular Cytogenetics 81
Reverse-Transcriptase-Polymerase Chain Reaction 83
New Hybridization-Based Methods for Fusion Transcript Detection 84
Applications of Next-Generation Sequencing to Gene Fusion Discovery or Diagnosis 84
Immunohistochemical Markers of Genetic Alterations 84
Major Pathogenetic Classes of Sarcomas 85
Sarcomas with Chimeric Transcription Factors 85
Ewing Sarcoma/Peripheral Neuroectodermal Tumor 86
Undifferentiated Small Round Cell Sarcomas with CIC-DUX4 88
Undifferentiated Small Round Cell Sarcomas with BCOR-CCNB3 88
Alveolar Rhabdomyosarcoma 88
Spindle Cell Rhabdomyosarcoma 89
Desmoplastic Small Round Cell Tumor 89
Clear Cell Sarcoma 89
Angiomatoid Fibrous Histiocytoma 89
Myxoid Liposarcoma 89
Extraskeletal Myxoid Chondrosarcoma 90
Mesenchymal Chondrosarcoma 90
Synovial Sarcoma 90
Alveolar Soft Part Sarcoma 90
Low-Grade Fibromyxoid Sarcoma 90
Epithelioid Hemangioendothelioma 91
Myoepithelioma of Soft Tissue 91
Solitary Fibrous Tumor 91
Myopericytoma with a t(7;12) 91
Myxoinflammatory Fibroblastic Sarcoma/Hemosiderotic Fibrolipomatous Tumor 91
Ossifying Fibromyxoid Tumor 92
Sarcomas with Genetic Deregulation of Kinase Signaling 92
Inflammatory Myofibroblastic Tumor 92
Infantile Fibrosarcoma 92
Dermatofibrosarcoma Protuberans/Giant Cell Fibroblastoma 92
Tenosynovial Giant Cell Tumor 93
Gastrointestinal Stromal Tumors 93
Sarcomas with Complex Karyotypes 94
High-Grade Pleomorphic Sarcomas 95
Atypical Lipomatous Neoplasm (Well-Differentiated Liposarcoma) and Dedifferentiated Liposarcoma 95
Leiomyosarcoma 96
Embryonal Rhabdomyosarcoma 96
PEComas 96
Neuroblastoma 96
Chromosome Changes in Benign Mesenchymal Tumors 96
Genetics of Familial Sarcomas and Their Sporadic Counterparts 97
Neurofibromatosis Type 1 and Malignant Peripheral Nerve Sheath Tumor 98
Familial Adenomatous Polyposis and Desmoids 99
Sarcomas in Hereditary Nonpolyposis Colorectal Cancer 99
Familial Rhabdoid Predisposition Syndrome and Malignant Extrarenal Rhabdoid Tumors 99
Contributions of Pan-Genomic Studies to Sarcoma Diagnosis and Classification 99
Acknowledgments 100
References 100
5 Fine-Needle Aspiration Biopsy of Soft Tissue Tumors 110
Chapter Contents 110
Introduction 110
Advantages and Disadvantages of Fine-Needle Aspiration 110
Myxoid Sarcomas 111
Spindle Cell Sarcomas 113
Pleomorphic Sarcomas 117
Polygonal Cell Sarcomas 119
Round Cell Sarcomas 121
Miscellaneous Sarcomas 121
Accuracy of Fine-Needle Aspiration 123
Grading and Fine-Needle Aspiration 124
Conclusions 124
References 124
6 Approach to the Diagnosis of Soft Tissue Tumors 127
Chapter Contents 127
Clinical Information 127
Biopsy Diagnosis 127
Frozen Section Diagnosis 128
Evaluation of Resection Specimens 128
Microscopic Examination 129
Immunohistochemistry 132
Molecular Tests 133
Diagnostic Nomenclature 133
Standardized Reporting of Soft Tissue Sarcomas 134
References 136
7 Immunohistochemistry for Analysis of Soft Tissue Tumors 137
Chapter Contents 137
Intermediate Filaments 137
Vimentin 137
Cytokeratins 138
Sarcomas with True Epithelial Differentiation: Epithelioid Sarcoma and Synovial Sarcoma 139
Anomalous Cytokeratin Expression 139
Smooth Muscle Cells and Smooth Muscle Tumors 139
Melanomas 139
Angiosarcomas 139
Small Blue Round Cell Tumors 142
Cytokeratin Expression in Other Sarcomas 142
Epithelial Membrane Antigen 144
Markers of Muscle Differentiation 144
Desmin 145
Actin 147
Myogenic Transcription Factors 148
Myoglobin and Other Less Commonly Used Markers 149
Recommendations for the Use of Muscle Markers 149
Markers of Nerve Sheath Differentiation 150
S-100 Protein 150
Claudin-1 151
GLUT-1 151
p75NTR 154
Neuroectodermal Markers 154
CD99 154
CD56 (Neural Cell Adhesion Molecule) 155
NB-84 155
NKX2.2 155
Markers of Melanocytic Differentiation 155
HMB-45 155
Melan-A 157
Microphthalmia Transcription Factor 157
PNL2 158
Tyrosinase 159
SOX10 159
Markers of Endothelial Differentiation 159
von Willebrand Factor (Factor VIII-Related Antigen) 160
CD34 (Human Hematopoietic Progenitor Cell Antigen) 161
CD31 (Platelet Endothelial Cell Adhesion Molecule-1) 161
FLI-1 and ERG Proteins 161
Claudin-5 161
Putative Markers of Lymphatic Endothelial Differentiation: VEGFR-3, Podoplanin (D2-40), and Prox1 163
Podoplanin (D2-40) 163
Prox1 163
Human Herpesvirus 8 (HHV-8) Latency Associated Nuclear Antigen (LANA) 163
Type IV Collagen 163
Recommendations for the Use of Vascular Markers 163
Markers of Gastrointestinal Stromal Tumors 164
CD117 (C-KIT) 164
Protein Kinase C-θ 164
Anoctamin-1 (ANO1, DOG1, TMEM16A) 165
Use of Immunohistochemistry as a Surrogate for the Presence of Tumor-Specific Molecular Alterations 167
FLI-1 and ERG as Markers of EFT 168
WT-1 as a Marker of the t(11;22)(13;q24) Translocation of DSRCT 168
TFE3 as a Marker of the der(17)t(X;17)(p11;q25) Translocation of ASPS 168
SMARCB1 (INI1) Expression Loss as a Marker of Monosomy or Homozygous Deletions of the hSNF5/INI-1/SMARCB1/BAF47 Gene 168
Anaplastic Lymphoma Kinase 169
Other Markers 170
TLE1 170
MUC4 171
CD68 172
β-Catenin 173
MDM2 and cdk4 174
Bcl-2 174
Prognostic Markers 175
Ki-67 175
p53 175
p21WAF1 175
p16 AND p27kip 175
Application of Immunohistochemistry to Sarcoma Diagnosis: Clinical Scenarios 175
The Undifferentiated Round Cell Tumor 175
Monomorphic Spindle Cell Tumors 176
Poorly Differentiated Epithelioid Tumor 176
Orphan Sarcomas 177
Conclusion 177
References 177
8 Benign Fibroblastic/Myofibroblastic Proliferations, Including Superficial Fibromatoses 188
Chapter Contents 188
Benign Fibroblastic/Myofibroblastic Proliferations 190
Nodular Fasciitis 190
Clinical Findings 190
Gross Findings 190
Microscopic Findings 191
Ossifying Fasciitis 194
Intravascular Fasciitis 194
Cranial Fasciitis 195
Immunohistochemical Findings 196
Cytogenetic and Molecular Genetic Features 200
Differential Diagnosis 200
Discussion 201
Proliferative Fasciitis 201
Clinical Findings 201
Pathologic Findings 201
Proliferative Myositis 202
Clinical Findings 204
Pathologic Findings 204
Differential Diagnosis 204
Discussion 204
Organ-Associated Pseudosarcomatous Myofibroblastic Proliferations 207
Clinical Findings 207
Pathologic Findings 207
Immunohistochemical Findings 209
Differential Diagnosis 210
Discussion 210
Ischemic Fasciitis (Atypical Decubital Fibroplasia) 211
Pathologic Findings 211
Differential Diagnosis 214
Discussion 214
Fibroma of Tendon Sheath 214
Pathologic Findings 214
Immunohistochemical Findings 215
Differential Diagnosis 215
Discussion 215
Pleomorphic Fibroma of the Skin 216
Nuchal-Type Fibroma 218
Gardner-Associated Fibroma 218
Clinical Findings 219
Pathologic Findings 219
Immunohistochemical Findings 220
Discussion 220
Elastofibroma 220
Clinical Findings 221
Pathologic Findings 221
Differential Diagnosis 223
Discussion 223
Nasopharyngeal Angiofibroma 224
Clinical Findings 224
Pathologic Findings 225
Immunohistochemical Findings 225
Discussion 226
Keloid 226
Clinical Findings 226
Pathologic Findings 227
Differential Diagnosis 227
Discussion 229
Desmoplastic Fibroblastoma (Collagenous Fibroma) 229
Pathologic Findings 229
Differential Diagnosis 229
Discussion 230
Intranodal Palisaded Myofibroblastoma 231
Pathologic Findings 231
Discussion 231
Mammary-Type Myofibroblastoma 233
Clinical Findings 233
Pathologic Findings 233
Cytogenetic and Molecular Genetic Findings 234
Differential Diagnosis 235
Discussion 235
Superficial Acral Fibromyxoma (Digital Fibromyxoma) 235
Clinical Findings 235
Pathologic Findings 236
Immunohistochemical Findings 237
Differential Diagnosis 237
Discussion 237
Angiofibroma of Soft Tissue 237
Clinical Findings 237
Pathologic Findings 237
Immunohistochemical Findings 238
Cytogenetic and Molecular Genetic Findings 238
Differential Diagnosis 239
Discussion 239
Superficial Fibromatoses 239
Palmar Fibromatosis 239
Clinical Findings 240
Concurrence of Palmar Fibromatosis With Other Diseases 240
Pathologic Findings 241
Immunohistochemical Findings 242
Cytogenetic and Molecular Genetic Findings 242
Differential Diagnosis 242
Discussion 243
Plantar Fibromatosis 243
Clinical Findings 243
Pathologic Findings 244
Discussion 245
Penile Fibromatosis (Peyronie Disease) 245
Clinical Findings 245
Pathologic Findings 246
Discussion 247
Knuckle Pads 247
References 248
9 Fibrous Tumors of Infancy and Childhood 256
Chapter Contents 256
Fibrous Hamartoma of Infancy 256
Clinical Findings 256
Pathologic Findings 256
Immunohistochemical Findings 258
Differential Diagnosis 260
Discussion 260
Infantile Digital Fibromatosis 260
Clinical Findings 260
Pathologic Findings 260
Immunohistochemical Findings 262
Discussion 262
Myofibroma and Myofibromatosis 263
Clinical Findings 263
Pathologic Findings 264
Immunohistochemical Findings 265
Differential Diagnosis 265
Discussion 266
Juvenile Hyaline Fibromatosis/Infantile Systemic Hyalinosis 267
Clinical Findings 267
Pathologic Findings 267
Cytogenetic and Molecular Genetic Findings 269
Differential Diagnosis 269
Discussion 269
Gingival Fibromatosis 269
Clinical Findings 269
Pathologic Findings 270
Differential Diagnosis 270
Discussion 270
Fibromatosis Colli 270
Clinical Findings 270
Pathologic Findings 271
Discussion 272
Infantile Fibromatosis (Lipofibromatosis) 272
Clinical Findings 272
Pathologic Findings 272
Differential Diagnosis 274
Discussion 275
Calcifying Aponeurotic Fibroma 276
Clinical Findings 276
Pathologic Findings 276
Differential Diagnosis 277
Discussion 279
Congenital and Acquired Muscular Fibrosis 279
Clinical Findings 279
Pathologic Findings 280
Discussion 280
Cerebriform Fibrous Proliferation (Proteus Syndrome) 280
Calcifying Fibrous Pseudotumor 280
References 283
10 Borderline and Malignant Fibroblastic/Myofibroblastic Tumors 288
Chapter Contents 288
Deep (Desmoid-Type) Fibromatoses 288
Extra-Abdominal Fibromatosis 288
Clinical Findings 288
Anatomic Location 289
Multicentric Fibromatoses 289
Pathologic Findings 289
Differential Diagnosis 290
Discussion 293
Abdominal Fibromatosis 294
Clinical Findings 294
Pathologic Findings 294
Discussion 294
Intra-Abdominal Fibromatosis 294
Pelvic Fibromatosis 295
Mesenteric Fibromatosis 295
Pathologic Findings 295
Differential Diagnosis 295
Mesenteric Fibromatosis in FAP/Gardner Syndrome 297
Discussion 297
Immunohistochemical Findings in Deep Fibromatoses 297
Clinical Behavior of Deep Fibromatoses 299
Treatment of Deep Fibromatoses 299
Congenital/Infantile Fibrosarcoma 300
Clinical Findings 300
Pathologic Findings 300
Immunohistochemical Findings 301
Cytogenic and Molecular Genetic Findings 303
Differential Diagnosis 303
Discussion 303
Inflammatory Myofibroblastic Tumor 304
Clinical Findings 304
Pathologic Findings 304
Immunohistochemical Findings 307
Cytogenetic and Molecular Genetic Findings 308
Differential Diagnosis 308
Discussion 309
Adult-Type Fibrosarcoma 310
Clinical Findings 310
Pathologic Findings 311
Immunohistochemical Findings 311
Cytogenetic and Molecular Genetic Findings 314
Differential Diagnosis 314
Discussion 315
Fibrosarcoma Variants 316
Fibrosarcoma, Sclerosing Epithelioid Type (Sclerosing Epithelioid Fibrosarcoma) 316
Clinical Findings 316
Pathologic Findings 316
Immunohistochemical Findings 317
Cytogenetic and Molecular Genetic Findings 317
Differential Diagnosis 317
Discussion 318
Myxofibrosarcoma (Fibrosarcoma, Myxoid Type) 318
Clinical Findings 318
Pathologic Findings 318
Cytogenetic and Molecular Genetic Findings 319
Differential Diagnosis 319
Discussion 322
Fibrosarcoma, Fibromyxoid Type (Low-Grade Fibromyxoid Sarcoma/Hyalinizing Spindle Cell Tumor with Giant Rosettes) 324
Clinical Findings 324
Pathologic Findings 324
Immunohistochemical Findings 330
Cytogenetic and Molecular Genetic Findings 330
Differential Diagnosis 330
Discussion 331
Fibrosarcomatous Change Arising in Dermatofibrosarcoma Protuberans 332
Postradiation Fibrosarcoma 332
Fibrosarcoma Arising in Burn Scars 332
Low-Grade Myofibroblastic Sarcoma (Myofibrosarcoma) 332
Clinical Findings 332
Pathologic Findings 332
Immunohistochemical Findings 333
Cytogenetic and Molecular Genetic Findings 334
Differential Diagnosis 334
Discussion 334
References 335
11 Benign Fibrohistiocytic and Histiocytic Tumors 341
Chapter Contents 341
Fibrous Histiocytoma 341
Clinical Findings 341
Microscopic Findings 342
Immunohistochemical Findings 347
Differential Diagnosis 349
Discussion 350
Variants of Benign Fibrous Histiocytoma 352
Cellular Fibrous Histiocytoma 353
Epithelioid Fibrous Histiocytoma 354
Aneurysmal Fibrous Histiocytoma 354
Minor Histologic Variants 355
Atypical Fibrous Histiocytoma 355
Dermatomyofibroma 355
Cellular Neurothekeoma 359
Clinical Features 359
Pathologic Features 360
Immunohistochemistry 361
Outcome 361
Differential Diagnosis 363
Solitary (Juvenile) Xanthogranuloma 363
Clinical Findings and Gross Appearance 363
Microscopic Findings 364
Differential Diagnosis 366
Clinical Behavior 367
Solitary Reticulohistiocytoma 367
Multicentric Reticulohistiocytosis 369
Pathologic Findings 369
Discussion 369
Xanthoma 369
Clinical Findings and Gross Appearance 370
Microscopic Findings 371
Discussion 371
Miscellaneous Histiocytic Reactions Resembling a Neoplasm 372
Infectious Disease 372
Malacoplakia 374
Extranodal (Soft Tissue) Rosai-Dorfman Disease 375
Histiocytic Reactions to Endogenous and Exogenous Material 377
Silica Reaction 377
Polyvinylpyrrolidone Granuloma 378
Granular Cell Reaction 380
Crystal-Storing Histiocytosis Resembling Rhabdomyoma 380
Cellular Spindled Histiocytic Pseudotumor Complicating Fat Necrosis 380
References 383
12 Fibrohistiocytic Tumors of Intermediate Malignancy 387
Chapter Contents 387
Dermatofibrosarcoma Protuberans 387
Clinical Findings 387
Gross Findings 388
Microscopic Findings 388
Immunohistochemical and Ultrastructural Findings 394
Cytogenetic and Molecular Genetic Features 396
Differential Diagnosis 397
Discussion 398
Sarcoma Arising in Dermatofibrosarcoma Protuberans (Fibrosarcomatous Variant of Dermatofibrosarcoma Protuberans) 398
Bednar Tumor (Pigmented Dermatofibrosarcoma Protuberans, Storiform Neurofibroma) 399
Giant Cell Fibroblastoma 400
Clinical Findings 401
Pathologic Findings 401
Differential Diagnosis 404
Discussion 404
Angiomatoid Fibrous Histiocytoma 404
Clinical Findings 404
Gross and Microscopic Findings 404
Immunohistochemical Features 408
Cytogenetic and Molecular Genetic Features 410
Discussion 411
Plexiform Fibrohistiocytic Tumor 411
Clinical Findings 411
Gross and Microscopic Findings 411
Ancillary Studies 414
Differential Diagnosis 414
Discussion 415
Soft Tissue Giant Cell Tumor of Low Malignant Potential 415
Clinical and Pathologic Features 415
Differential Diagnosis 417
Clinical Behavior 417
References 417
13 Undifferentiated Pleomorphic Sarcoma 421
Chapter Contents 421
Pleomorphic Sarcoma with a Specific Line of Differentiation 421
Atypical Fibroxanthoma (Undifferentiated Pleomorphic Sarcoma of the Skin) 422
Clinical Findings 422
Pathologic Findings 422
Differential Diagnosis 423
Discussion 425
Undifferentiated Pleomorphic Sarcoma 425
Clinical Findings 425
Etiologic Factors 426
Gross Findings 426
Microscopic Findings 426
Immunohistochemical Findings 430
Cytogenetic and Molecular Genetic Findings 434
Differential Diagnosis 434
Discussion 438
References 440
14 Benign Lipomatous Tumors 443
Chapter Contents 443
White Fat 443
Brown Fat 443
Molecular Biology of Benign Lipomatous Tumors 444
Immunohistochemistry of Benign Lipomatous Tumors 444
Classification of Benign Lipomatous Tumors 444
Lipoma 445
Age and Gender Incidence 445
Localization 445
Clinical Findings 445
Gross Findings 445
Microscopic Findings 445
Cytogenetic and Molecular Findings 447
Behavior and Treatment 447
Discussion 447
Multiple Lipomas 449
Angiolipoma 449
Myolipoma 452
Chondroid Lipoma 452
Clinical Findings 454
Pathologic Findings 454
Cytogenetic and Molecular Genetic Findings 454
Differential Diagnosis 454
Discussion 455
Spindle Cell/Pleomorphic Lipoma 456
Clinical Findings 456
Pathologic Findings 456
Immunohistochemical Findings 459
Cytogenetic and Molecular Genetic Findings 460
Differential Diagnosis 460
Discussion 463
Benign Lipoblastoma and Lipoblastomatosis 463
Clinical Findings 463
Pathologic Findings 464
Cytogenetic and Molecular Genetic Findings 465
Differential Diagnosis 465
Discussion 466
Angiomyolipoma 466
Myelolipoma 466
Intramuscular and Intermuscular Lipomas 468
Lipomas of Tendon Sheaths and Joints 469
Lumbosacral Lipoma 470
Neural Fibrolipoma (Lipofibromatous Hamartoma of Nerves) 470
Diffuse Lipomatosis 471
Symmetric Lipomatosis 472
Pelvic Lipomatosis 473
Steroid Lipomatosis 474
Nevus Lipomatosus Cutaneous Superficialis 474
Hibernoma 475
Clinical Findings 475
Pathologic Findings 475
Immunohistochemical Findings 477
Cytogenetic and Molecular Genetic Findings 478
Differential Diagnosis 478
Discussion 479
References 479
15 Liposarcoma 484
Chapter Contents 484
Criteria and Importance of Lipoblasts 485
Atypical Lipomatous Neoplasm (ALN)/Well-Differentiated Liposarcoma (WDL) 486
Clinical Findings 486
Gross and Microscopic Features 490
Differential Diagnosis 494
Cytogenetic and Molecular Findings 497
Immunohistochemical and Molecular Diagnosis of ALN/WDL and DL 498
Clinical Behavior 499
Dedifferentiated Liposarcoma 500
Clinical Features 500
Gross and Microscopic Features 500
Differential Diagnosis 502
Cytogenetic and Molecular Findings 505
Clinical Behavior 506
Myxoid Liposarcoma 506
Clinical Features 506
Gross and Microscopic Features 506
Differential Diagnosis 514
Cytogenetic and Molecular Findings 515
Clinical Course 515
Pleomorphic Liposarcoma 516
Spindle Cell Liposarcoma 518
Liposarcoma of Mixed or Unclassifiable Type 520
Liposarcoma in Children 521
So-Called Multicentric Liposarcoma 521
References 521
16 Benign Tumors of Smooth Muscle 524
Chapter Contents 524
Structure and Function of Smooth Muscle Cells 524
Cutaneous Leiomyoma (Leiomyoma Cutis) 525
Leiomyoma of Pilar Arrector Origin 525
Genital Leiomyomas 527
Angiomyoma (Vascular Leiomyoma) 527
Leiomyoma of Deep Soft Tissue 528
Leiomyomatosis Peritonealis Disseminata 534
Microscopic Findings 534
Ultrastructural Findings 535
Behavior and Treatment 537
Benign Genital Stromal Tumors 537
Angiomyofibroblastoma 537
Cellular Angiofibroma (Angiomyofibroblastoma-Like Tumor of the Male Genital Tract) 539
Aggressive Angiomyxoma 540
Clinical Findings 540
Pathologic Findings 540
Immunohistochemical and Ultrastructural Findings 543
Genetic Findings 543
Clinical Behavior and Outcome 543
Differential Diagnosis of Benign Genital Stromal Tumors 543
Miscellaneous Lesions Confused with Leiomyomas 546
References 546
17 Leiomyosarcoma 549
Chapter Contents 549
Retroperitoneal/Abdominal Leiomyosarcomas 549
Gross and Microscopic Findings 549
Histologic Variants of Leiomyosarcoma 553
Ultrastructural and Immunohistochemical Findings 556
Criteria of Malignancy 558
Differential Diagnosis 558
Genetic Findings 558
Clinical Behavior 559
Leiomyosarcomas of Somatic Soft Tissue 559
Cutaneous Leiomyosarcomas 559
Gross and Microscopic Findings 560
Clinical Behavior 560
Leiomyosarcomas of Vascular Origin 561
Clinical Findings 561
Inferior Vena Cava Leiomyosarcoma 561
Leiomyosarcomas of Other Veins 561
Pulmonary Artery Leiomyosarcoma 561
Gross and Microscopic Findings 562
Behavior and Treatment 562
Miscellaneous Sarcomas of Vascular Origin 562
Epstein-Barr Virus-Associated Smooth Muscle Tumors 563
References 566
18 GIST and EGIST 569
Chapter Contents 569
Epidemiology and Clinical Findings for Gastrointestinal Stromal Tumors 569
Macroscopic Findings for Gastrointestinal Stromal Tumors 570
Microscopic Findings for Gastrointestinal Stromal Tumors 570
Immunohistochemical Findings for Gastrointestinal Stromal Tumors 574
Ultrastructural Findings for Gastrointestinal Autonomic Nerve Tumors 579
Genetics of Gastrointestinal Stromal Tumors 579
Succinate Dehydrogenase Deficient Gastrointestinal Stromal Tumors 582
Pediatric Gastrointestinal Stromal Tumors 584
Gastrointestinal Stromal Tumor Syndromes 584
Behavior of Gastrointestinal Stromal Tumors 584
Treatment of Gastrointestinal Stromal Tumors 586
Histologic Assessment of Treated Gastrointestinal Stromal Tumors 588
References 588
19 Rhabdomyoma 591
Chapter Contents 591
Striated Muscle Tissue: Development and Structure 591
Classification of Rhabdomyomas 591
Cardiac Rhabdomyoma 591
Adult Rhabdomyoma 592
Pathologic Findings 593
Differential Diagnosis 594
Prognosis and Therapy 595
Fetal Rhabdomyoma 595
Clinical Features 595
Pathologic Findings 595
Differential Diagnosis 596
Prognosis and Therapy 596
Genital Rhabdomyoma 596
Rhabdomyomatous Mesenchymal Hamartoma of the Skin 598
Miscellaneous Lesions Mimicking Benign Striated Muscle Tumors 599
References 599
20 Rhabdomyosarcoma 601
Chapter Contents 601
Incidence of Rhabdomyosarcoma 601
Histologic Classification of Rhabdomyosarcoma 601
Age and Gender Distribution of Rhabdomyosarcoma 603
Clinical Features of Rhabdomyosarcoma 603
Gross Findings of Rhabdomyosarcoma 604
Rhabdomyosarcoma Subtypes 604
Embryonal Rhabdomyosarcoma 604
Cytogenetic and Molecular Genetic Findings 610
Spindle Cell Rhabdomyosarcoma 610
Embryonal Rhabdomyosarcoma, Botryoid Type 612
Alveolar Rhabdomyosarcoma 613
Pleomorphic Rhabdomyosarcoma 619
Sclerosing Rhabdomyosarcoma 622
Epithelioid Rhabdomyosarcoma 625
Special Diagnostic Procedures for Rhabdomyosarcoma 627
Special Stains 627
Immunohistochemical Findings 627
Differential Diagnosis of Rhabdomyosarcoma 630
Prognosis of Rhabdomyosarcoma 631
Recurrence of Rhabdomyosarcoma 633
Metastasis of Rhabdomyosarcoma 633
References 634
21 Benign Vascular Tumors and Malformations 639
Chapter Contents 639
Hemangiomas 639
Cherry Angioma (Senile Angioma, Campbell de Morgan Spots) 639
Infantile Hemangioma 640
Congenital Nonprogressive Hemangioma 643
Pyogenic Granuloma 644
Pregnancy-Related Pyogenic Granuloma (Granuloma Gravidarum) 648
Intravenous Pyogenic Granuloma 648
Epithelioid Hemangioma (Angiolymphoid Hyperplasia with Eosinophilia) 649
Vascular MalformationS 654
Cutaneous Capillovenous Malformation 654
Venous Malformation (Venous Hemangioma) 655
Arteriovenous Malformation (Arteriovenous Hemangioma) 656
Intramuscular Hemangioma 659
Angiomatosis 660
Miscellaneous Hemangiomas and Malformations 662
Verrucous Hemangioma (Hyperkeratotic Vascular Stain) 662
Hobnail Hemangioma (Targetoid Hemosiderotic Hemangioma) 664
Sinusoidal Hemangioma 664
Anastomosing Hemangioma 666
Acquired Tufted Angioma (Angioblastoma of Nakagawa) 666
Spindle Cell Hemangioma 667
Synovial Hemangioma 668
Hemangioma of Peripheral Nerves 671
Reactive Vascular Proliferations 671
Papillary Endothelial Hyperplasia 671
Vascular Transformation of Lymph Nodes 674
Glomeruloid Hemangioma 675
Bacillary (Epithelioid) Angiomatosis 675
Florid Vascular Proliferation of the Colon Secondary to Intussusception and Prolapse 677
References 679
22 Hemangioendothelioma: Vascular Tumors of Intermediate Malignancy 681
Chapter Contents 681
Vascular Tumor of Intermediate Malignancy 681
Epithelioid Hemangioendothelioma 681
Microscopic Features 681
Differential Diagnosis 681
Behavior and Treatment 685
Epithelioid Hemangioendotheliomas in Other Sites 687
Kaposiform Hemangioendothelioma 688
Hobnail (Dabska-Retiform) Hemangioendothelioma 693
Clinical Features 693
Microscopic Features 694
Immunohistochemical Findings 697
Discussion 698
Epithelioid Sarcoma-Like Hemangioendothelioma 698
Composite Hemangioendothelioma 698
References 701
23 Malignant Vascular Tumors 703
Chapter Contents 703
Angiosarcoma 703
Incidence 703
Etiologic Factors 703
Molecular-Genetic Findings 704
Clinical Subtypes 704
Primary Cutaneous Angiosarcoma 704
Ultrastructural Findings 711
Immunohistochemical Findings 711
Clinical Behavior 713
Angiosarcoma Associated with Lymphedema 713
Clinical Findings 713
Microscopic Findings 714
Angiosarcoma of the Breast 714
Differential Diagnosis 715
Angiosarcoma of Soft Tissue 715
Radiation-Induced Angiosarcoma 716
Prognostic Factors and Clinical Behavior 717
Atypical Vascular Lesion 717
Kaposi Sarcoma 723
Clinical Findings 723
Classic Kaposi Sarcoma 723
Endemic (African) Kaposi Sarcoma 723
Iatrogenic (Transplantation-Associated) Kaposi Sarcoma 724
AIDS-Related Kaposi Sarcoma 724
Microscopic Findings 724
Immunohistochemical Findings 728
Ultrastructural Observations 728
Differential Diagnosis 729
Behavior and Treatment 730
References 731
24 Tumors and Malformations of Lymphatic Vessels 733
Chapter Contents 733
Lymphatic Malformations (Lymphangioma, Cystic Hygroma) 733
Clinical Findings 734
Lymphatic Malformations of the Head and Neck 735
Intra-Abdominal Lymphatic Malformations 735
Cutaneous Lymphatic Malformations 736
Gross and Microscopic Findings 737
Behavior and Treatment 742
Lymphangiomatosis 742
Localized Massive Lymphedema 745
References 747
25 Perivascular Tumors 749
Chapter Contents 749
Classic (Sporadic) Glomus Tumor 749
Clinical Findings 750
Gross Findings 750
Ultrastructural and Immunohistochemical Findings 752
Behavior and Treatment 755
Glomuvenous Malformation (Glomangioma, Familial Glomangioma) 755
Glomangiomyoma 756
Glomangiomatosis (Diffuse Glomus Tumor) 756
Atypical and Malignant Glomus Tumors 759
Malignant Glomus Tumor 760
Glomus Tumor of Uncertain Malignant Potential 760
Symplastic Glomus Tumor 762
Myopericytoma 762
Hemangiopericytoma-Like Tumor of Nasal Passages 763
References 764
26 Benign Tumors and Tumor-Like Lesions of Synovial Tissue 766
Chapter Contents 766
Giant Cell Tumor of Tendon Sheath, Localized Type (Tenosynovial Giant Cell Tumor, Localized Type) 766
Clinical Findings 767
Gross Findings 767
Microscopic Findings 767
Differential Diagnosis 771
Immunohistochemical Findings 772
Cytogenetic and Molecular Genetic Findings 772
Discussion 772
Giant Cell Tumor of Tendon Sheath, Diffuse Type (Tenosynovial Giant Cell Tumor, Diffuse Type; Extra-Articular Pigmented Villonodular Synovitis) 773
Behavior and Treatment 777
Malignant Giant Cell Tumor of the Tendon Sheath/Pigmented Villonodular Synovitis 777
Miscellaneous Conditions Resembling Diffuse Giant Cell Tumor 779
References 782
27 Benign Tumors of Peripheral Nerves 784
Chapter Contents 784
Normal Anatomy 784
Traumatic (Amputation) Neuroma 786
Mucosal Neuroma 786
Pacinian Neuroma 787
Palisaded Encapsulated Neuroma 790
Morton Neuroma (Morton Metatarsalgia) 790
Ganglioneuroma 791
Nerve Sheath Ganglion 792
Neuromuscular Hamartoma (Neuromuscular Choristoma, Benign Triton Tumor) 796
Neurofibroma 796
Localized (Sporadic) Neurofibroma 797
Clinical Findings 797
Microscopic Findings 798
Neurofibromatosis 1 (NF1) 800
Clinical Findings 800
Variants of NF1 802
Pathologic Findings 802
Localized Neurofibroma 802
Plexiform Neurofibroma 803
Diffuse Neurofibroma 804
Pigmented Neurofibroma 804
Malignant Change in Neurofibromas 809
Discussion 813
Schwannoma 813
Clinical Findings 813
Gross Findings 814
Microscopic Findings 815
Ultrastructural and Immunohistochemical Findings 820
Discussion 823
Schwannoma with Degenerative Change (Ancient Schwannoma) 823
Cellular Schwannoma 824
Plexiform Schwannoma 828
Epithelioid Schwannoma 828
Neurofibromatosis 2 (Nf2; Bilateral Vestibular Schwannomas) 829
Schwannomatosis 831
Perineurioma 831
Intraneural Perineurioma 831
Soft Tissue (Extraneural) Perineurioma 833
Sclerosing Perineurioma 836
Reticular Perineurioma 837
Perineurial MPNST (Malignant Perineurioma) 837
Granular Cell Tumor 838
Pathologic Findings 838
Differential Diagnosis 842
Discussion 843
Malignant Granular Cell Tumor 843
Congenital (Gingival) Granular Cell Tumor 845
Nerve Sheath Myxoma 845
Extracranial Meningioma 847
Glial Heterotopias 850
References 851
28 Malignant Peripheral Nerve Sheath Tumors 855
Chapter Contents 855
Malignant Peripheral Nerve Sheath Tumor 855
Clinical Findings 855
Gross Findings 856
Microscopic Findings 857
Immunohistochemical Findings 863
Differential Diagnosis 866
Molecular and Cytogenetic Findings 866
Clinical Behavior 867
Malignant Peripheral Nerve Sheath Tumor with Rhabdomyoblastic Differentiation (Malignant Triton Tumor) 868
Malignant Peripheral Nerve Sheath Tumor with Glands (Glandular Malignant Schwannoma) 868
Malignant Peripheral Nerve Sheath Tumor with Angiosarcoma 871
Epithelioid Malignant Peripheral Nerve Sheath Tumor 871
Extraspinal (Soft Tissue) Ependymoma 876
References 877
29 Soft Tissue Tumors Showing Melanocytic Differentiation 880
Chapter Contents 880
(Malignant) Melanotic Schwannoma 880
Melanotic Neuroectodermal Tumor of Infancy (Retinal Anlage Tumor, Melanotic Progonoma) 884
Clinical Findings 884
Gross and Microscopic Findings 884
Discussion 885
Clear Cell Sarcoma of Tendon and Aponeurosis 886
Clinical Findings 886
Pathologic Findings 886
Differential Diagnosis 890
Discussion 891
Clear Cell Sarcoma-Like Tumor of Gastrointestinal Tract (Malignant Gastrointestinal Neuroectodermal Tumor) 894
Clinical Features 894
Pathologic Features 894
Cytogenetic and Molecular Genetic Features 894
Discussion 894
Differential Diagnosis 897
Perivascular Epithelioid Cell Family of Tumors 897
Angiomyolipoma 897
Clinical Findings 897
Pathologic Findings 897
Cytogenetic Findings 898
Differential Diagnosis 901
Discussion 901
Lymphangiomyoma and Lymphangiomyomatosis 901
Clinical Findings 902
Pathologic Findings 902
Differential Diagnosis 903
Discussion 903
PEComa (Excluding AML, LAM, and Pulmonary CCST) 903
Clinical Findings 907
Pathologic Findings 907
Immunohistochemical and Ultrastructural Findings 907
Cytogenetic Findings 911
Differential Diagnosis 911
Discussion 911
References 912
30 Cartilaginous and Osseous Soft Tissue Tumors 917
Chapter Contents 917
Extraskeletal Chondroma (Chondroma of Soft Parts) 918
Clinical Findings 918
Pathologic Findings 918
Differential Diagnosis 920
Discussion 922
Extraskeletal Mesenchymal Chondrosarcoma 922
Clinical Findings 923
Pathologic Findings 923
Cytogenetic and Molecular Genetic Findings 925
Differential Diagnosis 925
Discussion 926
Non-Neoplastic Heterotopic Ossifications 926
Myositis Ossificans 926
Clinical Findings 926
Pathologic Findings 927
Malignant Transformation of Myositis Ossificans 929
Differential Diagnosis 929
Discussion 930
Fibro-Osseous Pseudotumor of the Digits 930
Fibrodysplasia (Myositis) Ossificans Progressiva 932
Clinical Findings 932
Pathologic Findings 934
Genetic Aspects of Fibrodysplasia Ossificans Progressiva 935
Discussion 935
Extraskeletal Osteosarcoma 936
Clinical Findings 937
Pathogenesis 937
Radiation-Induced Extraskeletal Osteosarcoma 937
Pathologic Findings 938
Immunohistochemical Findings 943
Differential Diagnosis 943
Discussion 943
References 944
31 Miscellaneous Benign Soft Tissue Tumors and Pseudotumors 947
Chapter Contents 947
Tumoral Calcinosis 947
Clinical Findings 947
Pathologic Findings 948
Differential Diagnosis 949
Discussion 950
Intramuscular Myxoma 951
Clinical Findings 951
Multiple Intramuscular Myxomas and Fibrous Dysplasia 952
Pathologic Findings 953
Differential Diagnosis 953
Discussion 958
Juxta-Articular Myxoma 958
Cutaneous Myxoma (Superficial Angiomyxoma) 958
Pathologic Findings 959
Differential Diagnosis 960
Discussion 962
Carney Complex 962
Ganglion (Ganglion Cyst) 963
Amyloid Tumor (Amyloidoma) 963
References 966
32 Soft Tissue Tumors of Intermediate Malignancy of Uncertain Type 969
Chapter Contents 969
Ossifying Fibromyxoid Tumor of Soft Tissue 969
Clinical Findings 969
Pathologic Findings 969
Immunohistochemical and Ultrastructural Findings 973
Cytogenetic and Molecular Genetic Findings 973
Differential Diagnosis 977
Discussion 977
Line of Differentiation 978
Myxoinflammatory Fibroblastic Sarcoma (Inflammatory Myxohyaline Tumor of the Distal Extremities with Virocyte or Reed-Sternberg-Like Cells, Acral Myxoinflammatory Fibroblastic Sarcoma) 978
Clinical Findings 979
Pathologic Findings 979
Immunohistochemical and Ultrastructural Findings 980
Genetic Findings 985
Differential Diagnosis 986
Discussion 986
Pleomorphic Hyalinizing Angiectatic Tumor of Soft Parts 986
Clinical Findings 987
Pathologic Findings 987
Immunohistochemical and Ultrastructural Findings 990
Genetic Findings 990
Differential Diagnosis 991
Discussion 991
Myxoinflammatory Fibroblastic Sarcoma, Hemosiderotic Fibrolipomatous Tumor and Pleomorphic Hyalinizing Angiectatic Tumor: A Family of Related Neoplasms? 992
Myoepithelioma/Mixed Tumor of Soft Tissue (Parachordoma) 993
Clinical Findings 993
Pathologic Findings 993
Immunohistochemical and Ultrastructural Findings 995
Cytogenetic and Molecular Genetic Findings 1000
Differential Diagnosis 1000
Discussion 1002
Solitary Fibrous Tumor (Hemangiopericytoma) 1002
Clinical Features 1002
Pathologic Findings 1003
Immunohistochemical and Ultrastructural Findings 1010
Differential Diagnosis 1012
Cytogenetic Findings 1012
Discussion 1012
Variants of Solitary Fibrous Tumor 1014
Lipomatous Solitary Fibrous Tumor 1014
Meningeal (Cranial and Intraspinal) Hemangiopericytoma-Solitary Fibrous Tumor 1014
Solitary Fibrous Tumor with Giant Cells (Giant Cell Angiofibroma) 1014
Infantile Hemangiopericytoma 1017
Phosphaturic Mesenchymal Tumor 1018
Clinical Features 1019
Pathologic Findings 1019
Immunohistochemical and Ultrastructural Features 1019
Genetic Findings 1023
Differential Diagnosis 1023
References 1023
33 Malignant Soft Tissue Tumors of Uncertain Type 1028
Chapter Contents 1028
Ewing Family of Tumors (Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor) 1028
Clinical Features 1028
Pathologic Findings 1029
Ultrastructural Features 1037
Immunohistochemical Findings 1037
Cytogenetic and Molecular Genetic Findings 1039
Differential Diagnosis 1040
Clinical Behavior and Therapy 1045
Extraskeletal Myxoid Chondrosarcoma 1045
Clinical Findings 1045
Pathologic Findings 1046
Immunohistochemical Findings 1050
Cytogenetic and Molecular Genetic Findings 1050
Differential Diagnosis 1050
Discussion 1051
Synovial Sarcoma 1052
Clinical Findings 1052
Age and Gender Incidence 1052
Clinical Complaints 1052
Trauma 1052
Anatomic Location 1053
Radiographic Findings 1053
Gross Findings 1053
Microscopic Findings 1055
Biphasic Synovial Sarcoma 1055
Monophasic Fibrous Synovial Sarcoma 1060
Monophasic Epithelial Synovial Sarcoma (Epithelial-Predominant Synovial Sarcoma) 1062
Poorly Differentiated Synovial Sarcoma 1062
Special Staining Procedures 1064
Immunohistochemical Findings 1065
Ultrastructural Findings 1067
Cytogenetic and Molecular Genetic Findings 1067
Differential Diagnosis 1067
Differential Diagnosis of Biphasic Synovial Sarcoma 1067
Differential Diagnosis of Monophasic Fibrous Synovial Sarcoma 1068
Differential Diagnosis of Monophasic Epithelial (Epithelial-Predominant) Synovial Sarcoma 1068
Differential Diagnosis of Poorly Differentiated Synovial Sarcoma 1068
Discussion 1069
Recurrence and Metastasis 1069
Prognosis 1069
Therapy 1070
Line of Differentiation 1070
Alveolar Soft Part Sarcoma 1070
Clinical Findings 1070
Pathologic Findings 1071
Immunohistochemical Findings 1074
Ultrastructural Findings 1076
Cytogenetic and Molecular Genetic Findings 1076
Differential Diagnosis 1077
Clinical Behavior and Therapy 1077
Discussion 1078
Desmoplastic Small Round Cell Tumor 1079
Clinical Findings 1079
Pathologic Findings 1079
Immunohistochemical Findings 1079
Cytogenetic and Molecular Genetic Findings 1082
Differential Diagnosis 1083
Discussion 1083
CIC-Rearranged Family of Tumors 1084
Clinical Findings 1084
Pathologic Findings 1084
Cytogenetic and Molecular Genetic Findings 1084
Discussion 1085
Epithelioid Sarcoma 1086
Clinical Findings 1086
Pathologic Findings 1087
Differential Diagnosis 1092
Proximal-Type Epithelioid Sarcoma 1093
Immunohistochemical Findings 1095
Cytogenetic and Molecular Genetic Findings 1096
Clinical Course and Therapy 1096
Discussion 1097
Malignant Extrarenal Rhabdoid Tumor 1098
Pathologic Findings 1098
Immunohistochemical and Ultrastructural Findings 1101
Cytogenetic and Molecular Findings 1102
Discussion 1102
References 1103
Index 1113
A 1113
B 1116
C 1116
D 1120
E 1121
F 1124
G 1127
H 1129
I 1131
J 1133
K 1133
L 1133
M 1136
N 1141
O 1142
P 1143
Q 1146
R 1146
S 1148
T 1152
U 1153
V 1153
W 1154
X 1154
Z 1155
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