Nosé | Diagnostic Pathology: Familial Cancer Syndromes | Buch | 978-0-443-28640-7 | sack.de

Buch, Englisch, 1008 Seiten, Format (B × H): 210 mm x 297 mm, Gewicht: 450 g

Nosé

Diagnostic Pathology: Familial Cancer Syndromes


3rd Auflage
ISBN: 978-0-443-28640-7
Verlag: Elsevier Health Sciences

Buch, Englisch, 1008 Seiten, Format (B × H): 210 mm x 297 mm, Gewicht: 450 g

ISBN: 978-0-443-28640-7
Verlag: Elsevier Health Sciences


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. - 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

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Autoren/Hrsg.


Weitere Infos & Material


PART I: DIAGNOSES ASSOCIATED WITH SYNDROMES BY ORGAN
Section 1: Blood and Bone Marrow
Section 2: Bone and Soft Tissue
Section 3: Breast
Section 4: Endocrine
ADRENAL CORTEX
ADRENAL MEDULLA AND PARAGANGLIA
PANCREAS
PARATHYROID
PITUITARY
THYROID, MEDULLARY
THYROID, NONMEDULLARY
Section 5: Gastrointestinal
HEPATOBILIARY AND PANCREAS
TUBULAR GUT
Section 6: Genitourinary
BLADDER
KIDNEY
PROSTATE
RENAL PELVIS AND URETER
TESTICLE
Section 7: Gynecology
Section 8: Head and Neck
Section 9: Nervous System
Section 10: Pulmonary
Section 11: Skin

PART II: OVERVIEW OF SYNDROMES
Section 1: Introduction
Section 2: Syndromes

PART III: REFERENCE
Section 1: Molecular Factors


Nosé, Vania
Vania Nosé, MD, PhD, Professor of Pathology, Harvard Medical School, Pathologist and Consultant in Endocrine Pathology and Familial Syndromes, Massachusetts General Hospital, Boston, Massachusetts



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