Pheochromocytoma: Diagnosis, Localization, and Treatment
Karel Pacak, Graeme Eisenhofer, Jacques LendersBooks.org participates in affiliate programs including Bookshop.org and the Amazon Services LLC Associates Program. We may earn a commission from qualifying purchases made through links on this page, at no additional cost to you.
Synopsis
Pheochromocytomas are rare but treacherous catecholamine-producing tumors, which if missed or not properly treated, will almost invariably prove fatal. Prompt diagnosis is, therefore, essential for effective treatment, usually by surgical resection. The manifestations are diverse and the tumor can mimic a variety of conditions, often resulting in either erroneous diagnoses or a delayed diagnosis.
Reflecting the recent leaps in understanding this condition, Pheochromocytoma: Diagnosis, Localization, and Treatment provides a comprehensive update on the improvements in the diagnosis, localization, management and treatment of pheochromocytomas – providing you with the latest cutting edge science alongside best clinical practice. Written by the leading names in the field, the text details the significant developments in understanding the genetics and biology of the tumors, coupled with technological advances in the fields of analytical chemistry, genomics, molecular biology and nuclear medicine.
Doody Review Services
Reviewer:Irena Duka, MD(University of Chicago Medical Center)
Description:This overview of pheochromocytoma includes recent advances in genetics and future therapeutic modalities.
Purpose:It is intended as an up-to-date review of the recent advances in genetics, diagnosis, localization and treatment of pheochromocytoma. The authors have achieved this goal by describing the topic from both basic science and clinical perspectives.
Audience:Although written for endocrinologists and general practitioners, the book can be used by trainees as well.
Features:It covers pheochromocytoma in detail, including clinical presentation, diagnosis, and treatment. There is a thorough description of the physiology of the adrenergic system and the biochemical diagnosis of pheochromocytoma. All the important points are illustrated by tables, figures, and algorithms that make the book easy to read.
Assessment:The information in this book is up to date and useful. It can be used as a reference by any practitioner who wants to know more about pheochromocytoma.