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Diagnostic Pathology: Familial Cancer Syndromes, 3rd Edition

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Diagnostic Pathology: Familial Cancer Syndromes, 3rd Edition

Ürün kodu: 9780443286407

Yayınevi: Elsevier

Durum: BU KİTAP İÇİN ÖN SİPARİŞ ALINMAKTADIR. TESLİM SÜRESİ 6 - 8 HAFTADIR. BİLGİ ALMAK İÇİN MAĞAZAMIZI ARAYINIZ

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Description: 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.
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
Table Of Contents:
Part I: Diagnoses Associated With Syndromes by Organ Section 1: Blood and Bone Marrow Acute Lymphoblastic Leukemia and Non-Hodgkin Lymphoma Blood and Bone Marrow Table Section 2: Bone and Soft Tissue Chondrosarcoma Chordoma Malignant Peripheral Nerve Sheath Tumor Osteosarcoma Rhabdomyosarcoma Schwannoma Bone and Soft Tissue Table Section 3: Breast Breast Carcinoma Breast Table Section 4: Endocrine ADRENAL CORTEX Multiple Endocrine Neoplasia Type 5, MAX-Related Adrenal Cortical Adenoma Adrenal Cortical Carcinoma Adrenal Cortical Neoplasms in Children Primary Pigmented Nodular Adrenocortical Disease Adrenal Cortex Table ADRENAL MEDULLA AND PARAGANGLIA Adrenal Medullary Hyperplasia Neuroblastic Tumors of Adrenal Gland SDH-Deficient Pheochromocytoma and Paraganglioma Adrenal Medulla and Paraganglia Table PANCREAS MAFA-Related Familial Insulinomatosis Pancreatic Neuroendocrine Neoplasms Endocrine Pancreas Table PARATHYROID Primary Multiglandular Parathyroid Disease Atypical Parathyroid Tumor Parathyroid Adenoma Parathyroid Carcinoma Primary Parathyroid Hyperplasia Parathyroid Table PITUITARY Pituitary Blastoma Pituitary Adenoma Primary Pituitary Hyperplasia Pituitary Table THYROID, MEDULLARY Thyroid Follicular Nodular Disease Follicular Thyroid Adenoma with Papillary Architecture Thyroblastoma Kinase Fusion-Related Thyroid Carcinomas Follicular Cell-Derived Thyroid Carcinoma, High Grade Cribriform Morular Thyroid Carcinoma Syndromic Familial Follicular Cell-Derived Thyroid Tumors Nonsyndromic Familial Follicular Cell-Derived Thyroid Tumors C-Cell Hyperplasia Medullary Thyroid Carcinoma Thyroid, Medullary Carcinoma Table THYROID, NONMEDULLARY Follicular Thyroid Carcinoma Thyroid, Nonmedullary Carcinoma Table Section 5: Gastrointestinal HEPATOBILIARY AND PANCREAS Hepatoblastoma Hepatocellular Carcinoma Pancreatic Adenocarcinoma Biliary Tract/Liver/Pancreas Table 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 Section 6: Genitourinary BLADDER Bladder Urothelial Carcinoma Bladder Table KIDNEY Angiomyolipoma Clear Cell Renal Cell Carcinoma Cystic Nephroma HLRCC Syndrome-Associated Renal Cell Carcinoma 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 Section 7: Gynecology Cervical Carcinoma Fallopian Tube Carcinoma Ovarian Tumors Endometrial Carcinoma Gynecologic Tumors Section 8: Head and Neck Endolymphatic Sac Tumor Head and Neck Squamous Cell Carcinoma Head and Neck Table Salivary Glands Table Section 9: Nervous System Central Nervous System Eye Peripheral Nervous System Section 10: Pulmonary Adenocarcinoma, Lung Adenocarcinoma with Lepidic (Bronchioloalveolar) Predominant Pattern Lymphangioleiomyomatosis Neuroendocrine Tumor, Lung Pleuropulmonary Blastoma Lung Table Section 11: Skin BAP1-Inactivated Melanocytic Tumor Basal Cell Carcinoma Cutaneous Melanoma Cutaneous Squamous Cell Carcinoma Sebaceous Carcinoma Skin Table Part II: Overview of Syndromes Section 1: Introduction 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 Brooke-Spiegler Syndrome Carney Complex Colonic Carcinoma Syndromes Costello Syndrome Gastrointestinal Involvement in PTEN-Hamartoma Tumor Syndrome Denys-Drash Syndrome Diamond-Blackfan Anemia DICER1 Syndrome Down Syndrome Dyskeratosis Congenita Familial Acute Myeloid Leukemia and Myelodysplastic Syndrome Familial Adenomatous Polyposis Familial Cancer Syndromes in Colorectal Carcinoma Familial Chordoma Familial Gastrointestinal Stromal Tumor Familial Infantile Myofibromatosis Familial Isolated Hyperparathyroidism Familial Nonmedullary Thyroid Carcinoma Familial Paraganglioma Pheochromocytoma Syndrome Familial Testicular Tumor Familial Uveal Melanoma Familial Wilms Tumor Fanconi Anemia Glucagon Cell Hyperplasia and Neoplasia Breast/Ovarian Cancer Syndrome: BRCA1 Breast/Ovarian Cancer Syndrome: BRCA2 Hamartomatous Polyps, Cronkhite-Canada Juvenile Polyposis Syndrome Hamartomatous Polyps, Peutz-Jeghers Hereditary Diffuse Gastric Cancer Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome Hereditary Mixed Polyposis Syndrome Multiple Osteochondromas Hereditary Neuroblastoma Hereditary Pancreatic Cancer Syndrome Hereditary Papillary Renal Cell Carcinoma Hereditary Paraganglioma/Pheochromocytoma Syndromes Hereditary Prostate Cancer Hereditary Renal Epithelial Tumors, Others Hereditary Retinoblastoma Hereditary SWI/SNF Complex Deficiency Syndromes 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) 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) MUTYH-Associated Polyposis Neurofibromatosis Type 1 Neurofibromatosis Type 2 Nijmegen Breakage Syndrome Pancreatic Neuroendocrine Tumor Syndromes Hamartomatous Polyps, Peutz-Jeghers PTEN Hamartoma Tumor Syndromes RASopathies: Noonan Syndrome Rhabdoid Predisposition Syndrome Schwannomatosis Serrated Polyposis Shwachman-Diamond Syndrome Tumor Syndromes Predisposing to Osteosarcoma von Hippel-Lindau Syndrome Werner Syndrome/Progeria Wilms Tumor-Associated Syndromes Wiskott-Aldrich Syndrome Xeroderma Pigmentosum Epidermodysplasia Verruciformis Steatocystoma Multiplex Tuberous Sclerosis Complex Part III: Reference Section 1: Molecular Factors

ISBN	9780443286407
Basım Yılı	2025
Sayfa Sayısı	994
Yazar(lar)	Vania Nosé

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