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Pheochromocytomas, Paragangliomas and Disorders of the Sympathoadrenal System: Clinical Features, Diagnosis and Management / edited by Lewis Landsberg.

Contributor(s): Landsberg, Lewis., editor literario | SpringerLink (Online service)
Material type: materialTypeLabelE-bookSeries: (Medicine (Springer-11650)).Publisher: Cham : Springer International Publishing Springer International Publishing, 2018Description: 1 recurso en línea (XII, 220 páginas 47 ilustraciones, 17 ilustraciones a color).ISBN: 9783319770482.Subject: EndocrinologíaOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
Catecholamines -- Pathology of Pheochromocytoma and Paraganglioma -- Clinical Features of Pheochromocytoma and Paraganglioma -- Heritable and Syndromic Pheochromocytoma and Paraganglioma -- Pheochromocytoma and Paraganglioma in the Pediatric Population -- Diagnosis of Pheochromocytoma and Paraganglioma -- Localization of Pheochromocytoma and Paraganglioma -- Medical Management of Pheochromocytoma -- Anesthetic Management of Pheochromocytoma and Paraganglioma -- Surgery for Pheochromocytoma -- Pheochromocytoma in Pregnancy -- Pure Autonomic Failure: Diagnosis, Differential Diagnosis and Natural History -- Hypoglycemia-Associated Autonomic Failure in Diabetes -- The Sympathetic Nervous System in Hypertension.
Abstract: Providing a comprehensive review of the most up-to-date evidence, this book presents the latest biology, diagnosis and management for pheochromocytomas, paragangliomas and related disorders of the sympathoadrenal system. Many new areas, including genetic syndromes, have evolved, and these are insufficiently appreciated among practitioners. A discussion of the basics of catecholamine biology sets the stage for presentations of the pathology, clinical features, and diagnosis of these tumors, including localization and imaging. Medical, anesthetic and surgical management of pheochromocytomas and paragangliomas follow, including case material. Additional chapters discuss pheochromocytoma in pediatrics and in pregnancy, both pure and hypoglycemia-associated autonomic failure, and the role of the sympathetic nervous system in hypertension. These diseases are relatively rare, but many, if not most, go undiagnosed during life: If promptly diagnosed and appropriately treated, they are usually completely curable; if undiagnosed or mistreated, they are typically terminal. Bringing the most current knowledge to bear, Pheochromocytomas, Paragangliomas and Disorders of the Sympathoadrenal System will be a valuable resource for practicing endocrinologists, endocrine surgeons, internists and endocrine fellows faced with diagnosing and managing these conditions.
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Holdings
Item type Current library Collection Call number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC280.A3 P44 2018 EB (Browse shelf(Opens below)) Acceso electrónico eBook.08112176
Total holds: 0

Catecholamines -- Pathology of Pheochromocytoma and Paraganglioma -- Clinical Features of Pheochromocytoma and Paraganglioma -- Heritable and Syndromic Pheochromocytoma and Paraganglioma -- Pheochromocytoma and Paraganglioma in the Pediatric Population -- Diagnosis of Pheochromocytoma and Paraganglioma -- Localization of Pheochromocytoma and Paraganglioma -- Medical Management of Pheochromocytoma -- Anesthetic Management of Pheochromocytoma and Paraganglioma -- Surgery for Pheochromocytoma -- Pheochromocytoma in Pregnancy -- Pure Autonomic Failure: Diagnosis, Differential Diagnosis and Natural History -- Hypoglycemia-Associated Autonomic Failure in Diabetes -- The Sympathetic Nervous System in Hypertension.

Providing a comprehensive review of the most up-to-date evidence, this book presents the latest biology, diagnosis and management for pheochromocytomas, paragangliomas and related disorders of the sympathoadrenal system. Many new areas, including genetic syndromes, have evolved, and these are insufficiently appreciated among practitioners. A discussion of the basics of catecholamine biology sets the stage for presentations of the pathology, clinical features, and diagnosis of these tumors, including localization and imaging. Medical, anesthetic and surgical management of pheochromocytomas and paragangliomas follow, including case material. Additional chapters discuss pheochromocytoma in pediatrics and in pregnancy, both pure and hypoglycemia-associated autonomic failure, and the role of the sympathetic nervous system in hypertension. These diseases are relatively rare, but many, if not most, go undiagnosed during life: If promptly diagnosed and appropriately treated, they are usually completely curable; if undiagnosed or mistreated, they are typically terminal. Bringing the most current knowledge to bear, Pheochromocytomas, Paragangliomas and Disorders of the Sympathoadrenal System will be a valuable resource for practicing endocrinologists, endocrine surgeons, internists and endocrine fellows faced with diagnosing and managing these conditions.

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