A Rare Case Presenting with Symptoms of Familial Pheochromacytoma

Pheochromocytoma is a rare tumor in which seen an incidence of 1 per 100.000 in the general population. Pheochromocytoma is a catecholamine producing neuroendocrine tumor arising from adrenal medulla. A 46-year-old man experienced headache, sweating and palpitation referred to our hospital. Familial...

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Bibliographic Details
Main Authors: Mehtap Evran, Gamze Akkus, Murat Sert, Tamer Tetiker
Format: Article
Language:English
Published: Cukurova University 2015-09-01
Series:Çukurova Üniversitesi Tıp Fakültesi Dergisi
Subjects:
Online Access:http://www.scopemed.org/fulltextpdf.php?mno=175980