Diagnostic Pathology: Familial Cancer Syndromes
1. SECTION 1: INTRODUCTION - p. 473 2. Chapter 92: Pathology of Familial Tumor Syndromes - p. 473 3. Chapter 93: Clinical Diagnosis and Management of Familial/Hereditary Tumor Syndromes - p. 483 4. Chapter 94: Molecular Aspects of Familial/Hereditary Tumor Syndromes - p. 493 5. SECTION 2: SYNDROMES - p. 499 6. Chapter 95: Ataxia Telangiectasia - p. 499 7. Chapter 96: BAP1 Tumor Predisposition Syndrome - p. 503 8. Chapter 97: Basal Cell Nevus Syndrome/Gorlin Syndrome - p. 505 9. Chapter 98: Beckwith-Wiedemann Syndrome - p. 509 10. Chapter 99: Birt-Hogg-Dubé Syndrome - p. 517 11. Chapter 100: Bloom Syndrome - p. 521 12. Chapter 101: Brooke-Spiegler Syndrome - p. 523 13. Chapter 102: Carney Complex - p. 527 14. Chapter 103: Colonic Carcinoma Syndromes - p. 535 15. Chapter 104: Costello Syndrome - p. 539 16. Chapter 105: Denys-Drash Syndrome - p. 541 17. Chapter 106: Diamond-Blackfan Anemia - p. 545 18. Chapter 107: DICER1 Syndrome - p. 547 19. Chapter 108: Down Syndrome - p. 555 20. Chapter 109: Dyskeratosis Congenita - p. 559 21. Chapter 110: Familial Acute Myeloid Leukemia and Myelodysplastic Syndrome - p. 563 22. Chapter 111: Familial Adenomatous Polyposis - p. 567 23. Chapter 112: Familial Chordoma - p. 575 24. Chapter 113: Familial Gastrointestinal Stromal Tumor - p. 577 25. Chapter 114: Familial Infantile Myofibromatosis - p. 583 26. Chapter 115: Familial Isolated Hyperparathyroidism - p. 585 27. Chapter 116: Familial Nonmedullary Thyroid Carcinoma - p. 589 28. Chapter 117: Familial Paraganglioma Pheochromocytoma Syndrome - p. 595 29. Chapter 118: Familial Testicular Tumor - p. 599 30. Chapter 119: Familial Uveal Melanoma - p. 601 31. Chapter 120: Familial Wilms Tumor - p. 603 32. Chapter 121: Fanconi Anemia - p. 605 33. Chapter 122: Glucagon Cell Hyperplasia and Neoplasia - p. 607 34. Chapter 123: Breast/Ovarian Cancer Syndrome: BRCA1 - p. 609 35. Chapter 124: Breast/Ovarian Cancer Syndrome: BRCA2 - p. 615 36. Chapter 125: Hereditary Diffuse Gastric Cancer - p. 619 37. Chapter 126: Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome - p. 623 38. Chapter 127: Hereditary Mixed Polyposis Syndrome - p. 627 39. Chapter 128: Multiple Osteochondromas - p. 629 40. Chapter 129: Hereditary Neuroblastoma - p. 631 41. Chapter 130: Hereditary Pancreatic Cancer Syndrome - p. 635 42. Chapter 131: Hereditary Papillary Renal Cell Carcinoma - p. 639 43. Chapter 132: Hereditary Paraganglioma/Pheochromocytoma Syndromes - p. 641 44. Chapter 133: Hereditary Prostate Cancer - p. 649 45. Chapter 134: Hereditary Renal Epithelial Tumors, Others - p. 651 46. Chapter 135: Hereditary Retinoblastoma - p. 655 47. Chapter 136: Hereditary SWI/SNF Complex Deficiency Syndromes - p. 657 48. Chapter 137: Howel-Evans Syndrome/Keratosis Palmares and Plantares With Esophageal Cancer - p. 659 49. Chapter 138: Hyperparathyroidism-Jaw Tumor Syndrome - p. 661 50. Chapter 139: Juvenile Polyposis Syndrome - p. 667 51. Chapter 140: Li-Fraumeni Syndrome - p. 673 52. Chapter 141: Lynch Syndrome - p. 679 53. Chapter 142: McCune-Albright Syndrome - p. 685 54. Chapter 143: Melanoma/Pancreatic Carcinoma Syndrome - p. 691 55. Chapter 144: Multiple Endocrine Neoplasia Type 1 (MEN1) - p. 695 56. Chapter 145: Multiple Endocrine Neoplasia Type 2 (MEN2) - p. 703 57. Chapter 146: Multiple Endocrine Neoplasia Type 4 (MEN4) - p. 711 58. Chapter 147: MUTYH-Associated Polyposis - p. 717 59. Chapter 148: Neurofibromatosis Type 1 - p. 719 60. Chapter 149: Neurofibromatosis Type 2 - p. 727 61. Chapter 150: Nijmegen Breakage Syndrome - p. 733 62. Chapter 151: Pancreatic Neuroendocrine Tumor Syndromes - p. 735 63. Chapter 152: Hamartomatous Polyps, Peutz-Jeghers - p. 743 64. Chapter 153: PTEN-Hamartoma Tumor Syndromes - p. 749 65. Chapter 154: RASopathies: Noonan Syndrome - p. 757 66. Chapter 155: Rhabdoid Predisposition Syndrome - p. 761 67. Chapter 156: Schwannomatosis - p. 765 68. Chapter 157: Shwachman-Diamond Syndrome - p. 769 69. Chapter 158: Steatocystoma Multiplex - p. 771 70. Chapter 159: Tuberous Sclerosis Complex - p. 773 71. Chapter 160: Tumor Syndromes Predisposing to Osteosarcoma - p. 779 72. Chapter 161: von Hippel-Lindau Syndrome - p. 781 73. Chapter 162: Werner Syndrome/Progeria - p. 789 74. Chapter 163: Wilms Tumor-Associated Syndromes - p. 793 75. Chapter 164: Wiskott-Aldrich Syndrome - p. 795 76. Chapter 165: Xeroderma Pigmentosum - p. 797 77. Part III: Reference - p. 801 78. SECTION 1: MOLECULAR FACTORS - p. 801 79. Chapter 166: Molecular Factors Index - p. 801 80. INDEX - p. 823
Diagnostic Pathology: Familial Cancer Syndromes
1. SECTION 1: INTRODUCTION - p. 473 2. Chapter 92: Pathology of Familial Tumor Syndromes - p. 473 3. Chapter 93: Clinical Diagnosis and Management of Familial/Hereditary Tumor Syndromes - p. 483 4. Chapter 94: Molecular Aspects of Familial/Hereditary Tumor Syndromes - p. 493 5. SECTION 2: SYNDROMES - p. 499 6. Chapter 95: Ataxia Telangiectasia - p. 499 7. Chapter 96: BAP1 Tumor Predisposition Syndrome - p. 503 8. Chapter 97: Basal Cell Nevus Syndrome/Gorlin Syndrome - p. 505 9. Chapter 98: Beckwith-Wiedemann Syndrome - p. 509 10. Chapter 99: Birt-Hogg-Dubé Syndrome - p. 517 11. Chapter 100: Bloom Syndrome - p. 521 12. Chapter 101: Brooke-Spiegler Syndrome - p. 523 13. Chapter 102: Carney Complex - p. 527 14. Chapter 103: Colonic Carcinoma Syndromes - p. 535 15. Chapter 104: Costello Syndrome - p. 539 16. Chapter 105: Denys-Drash Syndrome - p. 541 17. Chapter 106: Diamond-Blackfan Anemia - p. 545 18. Chapter 107: DICER1 Syndrome - p. 547 19. Chapter 108: Down Syndrome - p. 555 20. Chapter 109: Dyskeratosis Congenita - p. 559 21. Chapter 110: Familial Acute Myeloid Leukemia and Myelodysplastic Syndrome - p. 563 22. Chapter 111: Familial Adenomatous Polyposis - p. 567 23. Chapter 112: Familial Chordoma - p. 575 24. Chapter 113: Familial Gastrointestinal Stromal Tumor - p. 577 25. Chapter 114: Familial Infantile Myofibromatosis - p. 583 26. Chapter 115: Familial Isolated Hyperparathyroidism - p. 585 27. Chapter 116: Familial Nonmedullary Thyroid Carcinoma - p. 589 28. Chapter 117: Familial Paraganglioma Pheochromocytoma Syndrome - p. 595 29. Chapter 118: Familial Testicular Tumor - p. 599 30. Chapter 119: Familial Uveal Melanoma - p. 601 31. Chapter 120: Familial Wilms Tumor - p. 603 32. Chapter 121: Fanconi Anemia - p. 605 33. Chapter 122: Glucagon Cell Hyperplasia and Neoplasia - p. 607 34. Chapter 123: Breast/Ovarian Cancer Syndrome: BRCA1 - p. 609 35. Chapter 124: Breast/Ovarian Cancer Syndrome: BRCA2 - p. 615 36. Chapter 125: Hereditary Diffuse Gastric Cancer - p. 619 37. Chapter 126: Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome - p. 623 38. Chapter 127: Hereditary Mixed Polyposis Syndrome - p. 627 39. Chapter 128: Multiple Osteochondromas - p. 629 40. Chapter 129: Hereditary Neuroblastoma - p. 631 41. Chapter 130: Hereditary Pancreatic Cancer Syndrome - p. 635 42. Chapter 131: Hereditary Papillary Renal Cell Carcinoma - p. 639 43. Chapter 132: Hereditary Paraganglioma/Pheochromocytoma Syndromes - p. 641 44. Chapter 133: Hereditary Prostate Cancer - p. 649 45. Chapter 134: Hereditary Renal Epithelial Tumors, Others - p. 651 46. Chapter 135: Hereditary Retinoblastoma - p. 655 47. Chapter 136: Hereditary SWI/SNF Complex Deficiency Syndromes - p. 657 48. Chapter 137: Howel-Evans Syndrome/Keratosis Palmares and Plantares With Esophageal Cancer - p. 659 49. Chapter 138: Hyperparathyroidism-Jaw Tumor Syndrome - p. 661 50. Chapter 139: Juvenile Polyposis Syndrome - p. 667 51. Chapter 140: Li-Fraumeni Syndrome - p. 673 52. Chapter 141: Lynch Syndrome - p. 679 53. Chapter 142: McCune-Albright Syndrome - p. 685 54. Chapter 143: Melanoma/Pancreatic Carcinoma Syndrome - p. 691 55. Chapter 144: Multiple Endocrine Neoplasia Type 1 (MEN1) - p. 695 56. Chapter 145: Multiple Endocrine Neoplasia Type 2 (MEN2) - p. 703 57. Chapter 146: Multiple Endocrine Neoplasia Type 4 (MEN4) - p. 711 58. Chapter 147: MUTYH-Associated Polyposis - p. 717 59. Chapter 148: Neurofibromatosis Type 1 - p. 719 60. Chapter 149: Neurofibromatosis Type 2 - p. 727 61. Chapter 150: Nijmegen Breakage Syndrome - p. 733 62. Chapter 151: Pancreatic Neuroendocrine Tumor Syndromes - p. 735 63. Chapter 152: Hamartomatous Polyps, Peutz-Jeghers - p. 743 64. Chapter 153: PTEN-Hamartoma Tumor Syndromes - p. 749 65. Chapter 154: RASopathies: Noonan Syndrome - p. 757 66. Chapter 155: Rhabdoid Predisposition Syndrome - p. 761 67. Chapter 156: Schwannomatosis - p. 765 68. Chapter 157: Shwachman-Diamond Syndrome - p. 769 69. Chapter 158: Steatocystoma Multiplex - p. 771 70. Chapter 159: Tuberous Sclerosis Complex - p. 773 71. Chapter 160: Tumor Syndromes Predisposing to Osteosarcoma - p. 779 72. Chapter 161: von Hippel-Lindau Syndrome - p. 781 73. Chapter 162: Werner Syndrome/Progeria - p. 789 74. Chapter 163: Wilms Tumor-Associated Syndromes - p. 793 75. Chapter 164: Wiskott-Aldrich Syndrome - p. 795 76. Chapter 165: Xeroderma Pigmentosum - p. 797 77. Part III: Reference - p. 801 78. SECTION 1: MOLECULAR FACTORS - p. 801 79. Chapter 166: Molecular Factors Index - p. 801 80. INDEX - p. 823
