Diagnostic Pathology: Familial Cancer Syndromes, 3rd Edition
Author :
Vania Nosé
Date of Publication: 08/2025
This item will be released on 11/08/2025. Pre-order now and we will deliver on the release date.
The new edition of Diagnostic Pathology: Familial Cancer Syndromes (DP3: Familial Cancers) is designed to help pathologists and oncologists distinguish familial tumors from their sporadic counterparts and advise patients regarding their possible risk ...view more
The new edition of Diagnostic Pathology: Familial Cancer Syndromes (DP3: Familial Cancers) is designed to help pathologists and oncologists distinguish familial tumors from their sporadic counterparts and advise patients regarding their possible risk of developing other tumors. The specific clinical, gross, microscopic, imaging, and molecular findings that form the backbone of DP3: Familial Cancers help physicians who diagnose and treat cancer accomplish this, ensuring that a possible syndromic association is not missed. Amid growing interest in hereditary/familial cancer syndromes within all pathology subspecialties, DP3: Familial Cancers is structured to present a significant number of its 180+ chapters by organ and organs involved by syndrome. The graphics-rich environment of DP3: Familial Cancers features thousands of images (including classic radiologic images to broaden the perspective), as well as informative, full-color medical illustrations and flowcharts. The book also contains hundreds of tables organized by body part and/or organ system that include selected existing genetic and familial cancers and identified associated genes, clinical features, recognized manifestations, and staging images/microscopic examples to bolster the information. The book addresses a wide range of inherited tumor syndromes to increase understanding of the gross and histologic features of syndromic-associated neoplasms as well as associated manifestations.
The new edition of Diagnostic Pathology: Familial Cancer Syndromes (DP3: Familial Cancers) is designed to help pathologists and oncologists distinguish familial tumors from their sporadic counterparts and advise patients regarding their possible risk of developing other tumors. The specific clinical, gross, microscopic, imaging, and molecular findings that form the backbone of DP3: Familial Cancers help physicians who diagnose and treat cancer accomplish this, ensuring that a possible syndromic association is not missed. Amid growing interest in hereditary/familial cancer syndromes within all pathology subspecialties, DP3: Familial Cancers is structured to present a significant number of its 180+ chapters by organ and organs involved by syndrome. The graphics-rich environment of DP3: Familial Cancers features thousands of images (including classic radiologic images to broaden the perspective), as well as informative, full-color medical illustrations and flowcharts. The book also contains hundreds of tables organized by body part and/or organ system that include selected existing genetic and familial cancers and identified associated genes, clinical features, recognized manifestations, and staging images/microscopic examples to bolster the information. The book addresses a wide range of inherited tumor syndromes to increase understanding of the gross and histologic features of syndromic-associated neoplasms as well as associated manifestations.
Key Features
Thoroughly up-to-date with more than 12 new chapters and updates to nearly a third of the book’s 180 existing chapters, as well as new or updated images, illustrations, and references
Hundreds of tables organized by body part and/or organ system that include selected existing genetic and familial cancers and identified associated genes, clinical features, recognized manifestations, and staging images/microscopic examples
An intuitive structure, an easy-to-navigate bulleted text format, and an image-rich layout that together allow for quick reference and comprehensive review of clinically relevant information
Author Information
By Vania Nosé, MD, PhD, Professor of Pathology, Harvard Medical School, Pathologist and Consultant in Endocrine Pathology and Familial Syndromes, Massachusetts General Hospital, Boston, Massachusetts, USA
Pathology of Familial Tumor Syndromes Clinical Diagnosis and Management of Familial/Hereditary Tumor Syndromes Molecular Aspects of Familial/Hereditary Tumor Syndromes
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
https://www.eu.elsevierhealth.com/diagnostic-pathology-familial-cancer-syndromes-9780443286407.html328333Diagnostic Pathology: Familial Cancer Syndromeshttps://www.eu.elsevierhealth.com/media/catalog/product/9/7/9780443286407_1.jpg264.59293.99EURInStock/Medicine and Surgery/Pathology9837174549828The new edition of <i>Diagnostic Pathology: Familial Cancer Syndromes </i>(DP3: Familial Cancers) is designed to help pathologists and oncologists distinguish familial tumors from their sporadic counterparts and advise patients regarding their possible risk of developing other tumors. The specific clinical, gross, microscopic, imaging, and molecular findings that form the backbone of DP3: Familial Cancers help physicians who diagnose and treat cancer accomplish this, ensuring that a possible syndromic association is not missed. Amid growing interest in hereditary/familial cancer syndromes within all pathology subspecialties, DP3: Familial Cancers is structured to present a significant number of its 180+ chapters by organ and organs involved by syndrome. The graphics-rich environment of DP3: Familial Cancers features thousands of images (including classic radiologic images to broaden the perspective), as well as informative, full-color medical illustrations and flowcharts. The book also contains hundreds of tables organized by body part and/or organ system that include selected existing genetic and familial cancers and identified associated genes, clinical features, recognized manifestations, and staging images/microscopic examples to bolster the information. The book addresses a wide range of inherited tumor syndromes to increase understanding of the gross and histologic features of syndromic-associated neoplasms as well as associated manifestations. The new edition of <i>Diagnostic Pathology: Familial Cancer Syndromes </i>(DP3: Familial Cancers) is designed to help pathologists and oncologists distinguish familial tumors from their sporadic counterparts and advise patients regarding their possible risk of developing other tumors. The specific clinical, gross, microscopic, imaging, and molecular findings that form the backbone of DP3: Familial Cancers help physicians who diagnose and treat cancer accomplish this, ensuring that a possible syndromic association is not missed. Amid growing interest in hereditary/familial cancer syndromes within all pathology subspecialties, DP3: Familial Cancers is structured to present a significant number of its 180+ chapters by organ and organs involved by syndrome. The graphics-rich environment of DP3: Familial Cancers features thousands of images (including classic radiologic images to broaden the perspective), as well as informative, full-color medical illustrations and flowcharts. The book also contains hundreds of tables organized by body part and/or organ system that include selected existing genetic and familial cancers and identified associated genes, clinical features, recognized manifestations, and staging images/microscopic examples to bolster the information. The book addresses a wide range of inherited tumor syndromes to increase understanding of the gross and histologic features of syndromic-associated neoplasms as well as associated manifestations.00add-to-cart97804432864072025ProfessionalBy Vania Nosé, MD, PhD20263Book210w x 297h (8.25" x 11.68")2,294 full-color imagesElsevier100811 Aug 2025NOT YET PUBLISHED Expected Release Date:%1By <STRONG>Vania Nosé</STRONG>, MD, PhD, Professor of Pathology, Harvard Medical School, Pathologist and Consultant in Endocrine Pathology and Familial Syndromes, Massachusetts General Hospital, Boston, Massachusetts, USABooksDiagnostic PathologyNoNoNoNoPlease SelectPlease SelectPlease Select
