Erschienen in:
01.02.2014 | e-Herz: Case study
Pheochromocytoma crisis presenting with cardiogenic shock
verfasst von:
Y.S. Chatzizisis, MD, PhD, A. Ziakas, C. Feloukidis, D. Paramythiotis, S. Hadjimiltiades, A. Iliadis, G. Basdanis, I. Styliadis
Erschienen in:
Herz
|
Ausgabe 1/2014
Einloggen, um Zugang zu erhalten
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.