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Diagnostic Pathology: Familial Cancer Syndromes

Diagnostic Pathology: Familial Cancer Syndromes

9780323712040
1 345,63 zł
1 143,79 zł Zniżka 201,84 zł Brutto
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Opis

This expert volume in the Diagnostic Pathology series is an excellent point-of-care resource for practitioners at all levels of experience and training. Physicians should have the knowledge derived from morphological findings to identify the likelihood of a cancer patient having an additional underlying familial syndrome- and to decide if that patient should undergo molecular genetic evaluation. This volume is specifically designed to help pathologists, oncologists, and other physicians who diagnose and treat cancer to recognize syndromes and syndrome- associated neoplasms and advise patients and their families on the possibility of a familial syndrome and their risk of developing other tumors. Diagnostic Pathology:: Familial Cancer Syndromes, second edition, is an easy-to-use, one-stop reference for information on hereditary cancer syndromes, including differential diagnosis and management, that offers a templated, highly formatted design; concise, bulleted text; and superior color images throughout.

Szczegóły produktu
Elsevier
63241
9780323712040
9780323712040

Opis

Rok wydania
2020
Numer wydania
2
Oprawa
twarda
Liczba stron
896
Wymiary (mm)
216 x 276
Waga (g)
2720
  • I. Diagnosis Associated With Syndromes by Organ

    Breast

    Breast Carcinoma, Female

    Breast Carcinoma, Male

    Breast Table

    Blood and Bone Marrow

    Acute Lymphoblastic Leukemia and Non-Hodgkin Lymphoma

    Acute Myeloid Leukemia and Myelodysplastic Syndrome

    Blood and Bone Marrow Table

    Bone and Soft Tissue

    Chondrosarcoma

    Chordoma

    Malignant Peripheral Nerve Sheath Tumor

    Osteosarcoma

    Rhabdomyosarcoma

    Schwannoma

    Bone and Soft Tissue Table

    Head and Neck

    Endolymphatic Sac Tumor

    Squamous Cell Carcinoma

    Head and Neck Table

    Salivary Glands Table

    Endocrine

    Adrenal Cortex

    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

    Neuroblastoma

    Pheochromocytoma and Paraganglioma

    Adrenal Medulla and Paraganglia Table

    Pancreas

    Pancreatic Neuroendocrine Neoplasms

    Pancreas Table

    Parathyroid

    Parathyroid Adenoma

    Parathyroid Carcinoma

    Parathyroid Hyperplasia

    Parathyroid Table

    Pituitary

    Pituitary Adenoma

    Pituitary Hyperplasia

    Pituitary Table

    Thyroid, Medullary

    C-Cell Hyperplasia

    Medullary Thyroid Carcinoma

    Thyroid, Medullary Table

    Thyroid, Nonmedullary

    Familial Thyroid Carcinoma

    Follicular Thyroid Carcinoma

    Thyroid, Nonmedullary Table

    Gastrointestinal

    Tubular Gut

    Colon Adenoma

    Esophageal Adenocarcinoma

    Esophageal Squamous Cell Carcinoma

    Gastric Adenocarcinoma

    Gastrointestinal Stromal Tumor

    Hamartomatous Polyps of GI Tract

    Small Bowel Adenocarcinoma

    Colon/Rectum Table

    Esophagus/Stomach/Small Bowel Table

    Tubular Gut Table

    Hepatobiliary and Pancreas

    Biliary Tract Neoplasia

    Hepatoblastoma

    Hepatocellular Carcinoma

    Pancreatic Adenocarcinoma

    Biliary Tract/Liver/Pancreas Table

    Hepatobiliary and Pancreas Table

    Genitourinary

    Bladder

    Bladder Table

    Kidney

    Angiomyolipoma

    Clear Cell Renal Cell Carcinoma

    HLRCC Syndrome-Associated Renal Cell Carcinoma

    Papillary Renal Cell Carcinoma

    Renal Oncocytoma, Chromophobe, and Hybrid Tumors

    Wilms Tumor

    Kidney Table

    Prostate

    Prostate Table

    Renal Pelvis and Ureter

    Renal Pelvis and Ureter Table

    Testicle

    Germ Cell Tumor

    Sertoli Cell Neoplasms

    Testicle Table

    Gynecology

    Cervical Tumors

    Fallopian Tube Tumors

    Ovarian Tumors

    Uterine Tumors

    Cervix

    Endometrium

    Fallopian Tube

    Ovary

    Nervous System

    Central Nervous System

    Eye

    Peripheral Nervous System

    Pulmonary

    Adenocarcinoma, Lung

    Adenocarcinoma With Lepidic (Bronchioloalveolar) Predominant Pattern

    Lymphangioleiomyomatosis

    Neuroendocrine Carcinoma, Lung

    Pleuropulmonary Blastoma

    Lung Table

    Skin

    BAP1-Inactivated Melanocytic Tumor

    Basal Cell Carcinoma

    Cutaneous Melanoma

    Cutaneous Squamous Cell Carcinoma

    Sebaceous Carcinoma

    Skin Table

    II. Overview of Syndromes

    Introduction

    Pathology of Familial Tumor Syndromes

    Clinical Diagnosis and Management of Familial/Hereditary Tumor Syndromes

    Molecular Aspects of Familial/Hereditary Tumor Syndromes

    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

    Costello Syndrome

    Cystic Nephroma Syndrome

    Denys-Drash Syndrome

    Diamond-Blackfan Anemia

    DICER1 Syndrome

    Down Syndrome

    Dyskeratosis Congenita

    Familial Acute Myeloid Leukemia and Myelodysplastic Syndrome

    Familial Adenomatous Polyposis

    Familial Chordoma

    Familial Gastrointestinal Stromal Tumor

    Familial Infantile Myofibromatosis

    Familial Isolated Hyperparathyroidism

    Familial Medullary Thyroid Carcinoma

    Familial Nonmedullary Thyroid Carcinoma

    Familial Paraganglioma-Pheochromocytoma Syndrome

    Familial Testicular Tumor

    Familial Uveal Melanoma

    Familial Wilms Tumor

    Fanconi Anemia

    GATA2 Spectrum Disorders

    Glucagon Cell Hyperplasia and Neoplasia

    Hereditary Breast/Ovarian Cancer Syndrome: BRCA1

    Hereditary Breast/Ovarian Cancer Syndrome: BRCA2

    Hereditary Diffuse Gastric Cancer

    Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome (HLRCC)

    Hereditary Multiple Exostosis

    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

    Heritable Gastrointestinal Stromal Tumors Syndromes

    Howel-Evans Syndrome/Keratosis Palmares and Plantares With Esophageal Cancer

    Hyperparathyroidism-Jaw Tumor Syndrome

    Juvenile Polyposis Syndrome

    Li-Fraumeni Syndrome/Li-Fraumeni-Like Syndrome

    Lynch 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)

    MYH-Associated Polyposis

    Neurofibromatosis Type 1

    Neurofibromatosis Type 2

    Nijmegen Breakage Syndrome

    Pancreatic Neuroendocrine Tumor Syndromes

    *PDGFRA*-Mutant Syndrome

    Peutz-Jeghers Syndrome

    PTEN Hamartoma Tumor Syndromes

    RASopathies: Noonan Syndrome

    Rhabdoid Predisposition Syndrome

    Schwannomatosis

    Shwachman-Diamond Syndrome

    Steatocystoma Multiplex

    Succinate Dehydrogenase (SDH)-Deficient Renal Cell Carcinoma

    Tuberous Sclerosis Complex

    Tumor Syndromes Predisposing to Osteosarcoma

    von Hippel-Lindau Syndrome

    Werner Syndrome/Progeria

    Wilms Tumor-Associated Syndrome

    Wiskott-Aldrich Syndrome

    Xeroderma Pigmentosum

    Reference

    Molecular Factors

    Molecular Factors Index

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