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...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Cukurova University
2015-09-01
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Series: | Çukurova Üniversitesi Tıp Fakültesi Dergisi |
Subjects: | |
Online Access: | http://www.scopemed.org/fulltextpdf.php?mno=175980 |