| Literature DB >> 23483222 |
Y S Chatzizisis1, A Ziakas, C Feloukidis, D Paramythiotis, S Hadjimiltiades, A Iliadis, G Basdanis, I Styliadis.
Abstract
Pheochromocytoma is a catecholamine-secreting tumor of the adrenal glands whose typical presentation includes the triad of headache, palpitations, and diaphoresis. Pheochromocytoma crisis is an urgent medical condition whose diagnosis and management constitute a challenge for physicians. We present the case of a 55-year-old man who developed cardiogenic shock in the setting of a pheochromocytoma crisis. After stabilizing blood pressure with combined administration of α- and β-blockers, the tumor was surgically removed. Our diagnostic and therapeutic challenges are discussed.Entities:
Mesh:
Year: 2013 PMID: 23483222 DOI: 10.1007/s00059-013-3778-2
Source DB: PubMed Journal: Herz ISSN: 0340-9937 Impact factor: 1.443