Author/Authors
Evran, Mehtap Cukurova University - Medical Faculty - Department of Internal Medicine, Division of Endocrinology, Turkey , Akkuş, Gamze Cukurova University - Medical Faculty - Department of Internal Medicine, Division of Endocrinology, Turkey , Sert, Murat Cukurova University - Medical Faculty - Department of Internal Medicine, Division of Endocrinology, Turkey , Tetiker, Tamer Cukurova University - Medical Faculty - Department of Internal Medicine, Division of Endocrinology, Turkey
Title Of Article
A Rare Case Presenting with Symptoms of Familial Pheochromacytoma
شماره ركورد
24070
Abstract
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 pheocromocytoma was detected. We presented this case as whole family members had suffered from morbidities and deaths due to this disorder.
From Page
593
NaturalLanguageKeyword
Pheocromocytoma , familial disorder , hypertension
JournalTitle
Cukurova Medical Journal
To Page
596
JournalTitle
Cukurova Medical Journal
Link To Document