Diagnostic Pathology: Familial Cancer Syndromes
by Vania Nosé
3rd Edition
Publisher: Elsevier Health Sciences
Book Details
| Print ISBN | 9780443286407 |
| eText ISBN | 9780443286414 |
| Publisher | Elsevier Health Sciences |
| Publishing Year | 2025 |
| Edition | 3rd Edition |
| Language | English |
Diagnostic Pathology: Familial Cancer Syndromes, 3rd Edition, written by Vania Nosé, is a comprehensive reference work detailing the diagnostic pathology of hereditary cancer conditions. Published by Elsevier as part of the Diagnostic Pathology series, the volume provides systematic coverage of syndromic-associated neoplasms to support accurate histopathologic identification, differential diagnosis, and disease management across anatomical sites.
The text follows a structured three-part organization to connect organ-specific findings with underlying genetic etiology. Part I features nearly 100 chapters detailing specific diagnoses grouped by organ and body system. Part II includes more than 80 chapters that examine major inherited syndromes and cross-reference them directly with corresponding clinical and pathologic diagnoses. Part III supplies an updated Molecular Factors Index describing known genes associated with familial cancer syndromes.
Updated throughout, this edition incorporates modern classifications based on the 2025 WHO Classification of Tumours: Genetic Tumour Syndromes. The text provides structured guidance for practicing pathologists, pathology residents, fellows, oncologists, and medical students examining inherited tumor syndromes in daily clinical practice and academic study.
Table of Contents
Chapter Section 1: Blood and Bone Marrow
- • Acute Lymphoblastic Leukemia and Non-Hodgkin Lymphoma
- • Blood and Bone Marrow Table
Chapter Section 2: Bone and Soft Tissue
- • Chondrosarcoma
- • Chordoma
- • Malignant Peripheral Nerve Sheath Tumor
- • Osteosarcoma
- • Rhabdomyosarcoma
- • Schwannoma
- • Bone and Soft Tissue Table
Chapter Section 3: Breast
- • Breast Carcinoma
- • Breast Table
Chapter Section 4: Endocrine
- • ADRENAL CORTEX
- • Adrenal Cortical Adenoma
- • Adrenal Cortical Carcinoma
- • Adrenal Cortical Neoplasms in Children
- • Adrenocortical Hyperplasia and Adrenocortical Nodular Disease
- • Primary Pigmented Nodular Adrenocortical Disease
- • Adrenal Cortex Table
- • ADRENAL MEDULLA AND PARAGANGLIA
- • Adrenal Medullary Hyperplasia
- • Pheochromocytoma and Paraganglioma
- • Neuroblastic Tumors of Adrenal Gland
- • Adrenal Medulla and Paraganglia Table
- • PANCREAS
- • Pancreatic Neuroendocrine Neoplasms
- • Endocrine Pancreas Table
- • PARATHYROID
- • Atypical Parathyroid Tumor
- • Parathyroid Adenoma
- • Parathyroid Carcinoma
- • Primary Multiglandular Parathyroid Disease
- • Parathyroid Table
- • PITUITARY
- • Pituitary Blastoma
- • Pituitary Neuroendocrine Tumor/Pituitary Adenoma (PitNET)
- • Pituitary Table
- • THYROID, MEDULLARY
- • C-Cell Hyperplasia
- • Medullary Thyroid Carcinoma
- • Thyroid, Medullary Carcinoma Table
- • THYROID, NONMEDULLARY
- • Thyroid Follicular Nodular Disease
- • Follicular Thyroid Adenoma With Papillary Architecture
- • Thyroblastoma
- • Kinase Fusion-Related Thyroid Carcinomas
- • Nonsyndromic Familial Follicular Cell-Derived Thyroid Carcinoma
- • Syndromic Familial Follicular Cell-Derived Thyroid Carcinoma
- • Cribriform Morular Thyroid Carcinoma
- • Follicular Cell-Derived Thyroid Carcinoma, High Grade
- • Follicular Thyroid Carcinoma
- • Thyroid, Nonmedullary Carcinoma Table
Chapter Section 5: Gastrointestinal
- • HEPATOBILIARY AND PANCREAS
- • Hepatoblastoma
- • Hepatocellular Carcinoma
- • Pancreatic Adenocarcinoma
- • TUBULAR GUT
- • Colonic Adenomas
- • Esophageal Adenocarcinoma
- • Esophageal Squamous Cell Carcinoma
- • Gastric Adenocarcinoma
- • Gastrointestinal Stromal Tumor
- • Hamartomatous Polyposis Syndromes
- • Small Bowel Adenocarcinoma
- • Colon/Rectum Table
- • Esophagus/Stomach/Small Bowel Table
Chapter Section 6: Genitourinary
- • BLADDER
- • Bladder Urothelial Carcinoma
- • Bladder Table
- • KIDNEY
- • Angiomyolipoma
- • Clear Cell Renal Cell Carcinoma
- • Cystic Nephroma
- • Papillary Renal Cell Carcinoma
- • Renal Oncocytoma, Chromophobe, and Hybrid Tumors
- • Succinate Dehydrogenase-Deficient Renal Cell Carcinoma
- • Wilms Tumor
- • Kidney Table
- • PROSTATE
- • Prostate Carcinoma
- • Prostate Table
- • RENAL PELVIS AND URETER
- • Renal Urothelial Carcinoma
- • Ureter Urothelial Carcinoma
- • Renal Pelvis and Ureter Table
- • TESTICLE
- • Germ Cell Tumor
- • Sertoli Cell Neoplasms
- • Testicle Table
Chapter Section 7: Gynecology
- • Cervical Carcinoma
- • Fallopian Tube Carcinoma
- • Ovarian Tumors
- • Endometrial Carcinoma
- • Gynecologic Tumors
Chapter Section 8: Head and Neck
- • Endolymphatic Sac Tumor
- • Head and Neck Squamous Cell Carcinoma
- • Head and Neck Table
- • Salivary Glands Table
Chapter Section 9: Nervous System
- • Central Nervous System Table
- • Eye Table
- • Peripheral Nervous System Table
Chapter Section 10: Pulmonary
- • Adenocarcinoma, Lung
- • Adenocarcinoma With Lepidic (Bronchioloalveolar) Predominant Pattern
- • Lymphangioleiomyomatosis
- • Neuroendocrine Tumor, Lung
- • Pleuropulmonary Blastoma
- • Lung Table
Chapter Section 11: Skin
- • BAP1-Inactivated Melanocytic Tumor
- • Basal Cell Carcinoma
- • Cutaneous Melanoma
- • Cutaneous Squamous Cell Carcinoma
- • Sebaceous Carcinoma
- • Skin Table
Chapter Section 1: Introduction
- • Pathology of Familial Tumor Syndromes
- • Clinical Diagnosis and Management of Familial/Hereditary Tumor Syndromes
- • Molecular Aspects of Familial/Hereditary Tumor Syndromes
Chapter Section 2: Syndromes
- • Ataxia-Telangiectasia
- • BAP1 Tumor Predisposition Syndrome
- • Basal Cell Nevus Syndrome/Gorlin Syndrome
- • Beckwith-Wiedemann Syndrome
- • Birt-Hogg-Dubé Syndrome
- • Bloom Syndrome
- • Breast/Ovarian Cancer Syndrome: BRCA1
- • Breast/Ovarian Cancer Syndrome: BRCA2
- • Brooke-Spiegler Syndrome
- • Carney Complex
- • Colonic Carcinoma Syndromes
- • Costello Syndrome
- • Denys-Drash Syndrome
- • Diamond-Blackfan Anemia
- • DICER1 Syndrome
- • Down Syndrome
- • Dyskeratosis Congenita
- • Epidermodysplasia Verruciformis
- • Hematologic Neoplasm With Germline Predisposition
- • Familial Adenomatous Polyposis
- • Familial Cancer Syndromes in Colorectal Carcinoma
- • Familial Chordoma
- • Familial Gastrointestinal Stromal Tumor
- • Familial and Hereditary Papillary Renal Cell Carcinoma
- • Familial and Hereditary Prostate Cancer
- • Familial Infantile Myofibromatosis
- • Familial Isolated Hyperparathyroidism
- • Familial Thyroid Carcinoma
- • Familial Pheochromocytoma and Paraganglioma Syndrome
- • Familial Testicular Tumor
- • Familial Uveal Melanoma
- • Familial Wilms Tumor
- • Fanconi Anemia
- • Glucagon Cell Hyperplasia and Neoplasia
- • Hereditary Gastric and Breast Cancer Syndrome
- • Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome
- • Hereditary Mixed Polyposis Syndrome
- • Hereditary Neuroblastoma
- • Hereditary Pancreatic Cancer Syndrome
- • Hereditary Paraganglioma/Pheochromocytoma Syndromes
- • Hereditary Renal Epithelial Tumors, Others
- • Hereditary Retinoblastoma
- • Hereditary SWI/SNF Complex Deficiency Syndromes
- • HLRCC Syndrome-Associated Renal Cell Carcinoma
- • Howel-Evans Syndrome/Keratosis Palmares and Plantares With Esophageal Cancer
- • Hyperparathyroidism-Jaw Tumor Syndrome
- • Juvenile Polyposis Syndrome
- • Li-Fraumeni Syndrome
- • Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer Syndrome)
- • MAFA-Related Familial Insulinomatosis
- • McCune-Albright Syndrome
- • Melanoma/Pancreatic Carcinoma Syndrome
- • Multiple Endocrine Neoplasia Type 1 (MEN1)
- • Multiple Endocrine Neoplasia Type 2 (MEN2)
- • Multiple Endocrine Neoplasia Type 4 (MEN4)
- • Multiple Endocrine Neoplasia Type 5, MAX-Related
- • Multiple Osteochondromas
- • MUTYH-Associated Polyposis
- • Neurofibromatosis Type 1
- • NF2-Related Schwannomatosis
- • Nijmegen Breakage Syndrome
- • Pancreatic Neuroendocrine Tumor Syndromes
- • Hamartomatous Polyps, Peutz-Jeghers Syndrome
- • PTEN-Hamartoma Tumor Syndromes
- • PTEN-Hamartoma Tumor Syndrome: Gastrointestinal Involvement
- • RASopathies: Noonan Syndrome
- • Rhabdoid Predisposition Syndrome
- • Schwannomatosis
- • Serrated Polyposis
- • Shwachman-Diamond Syndrome
- • Steatocystoma Multiplex
- • Tuberous Sclerosis Complex
- • Tumor Syndromes Predisposing to Osteosarcoma
- • von Hippel-Lindau Syndrome
- • Werner Syndrome/Progeria
- • Wilms Tumor-Associated Syndromes
- • Wiskott-Aldrich Syndrome
- • Xeroderma Pigmentosum
Chapter Section 1: Molecular Factors
- • Molecular Factors Index
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