Pheochromocytoma crisis presenting with cardiogenic shock

Y. S. Chatzizisis, A. Ziakas, C. Feloukidis, D. Paramythiotis, S. Hadjimiltiades, A. Iliadis, G. Basdanis, I. Styliadis

Research output: Contribution to journalArticle

2 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)156-160
Number of pages5
JournalHerz
Volume39
Issue number1
DOIs
StatePublished - Feb 2014

Keywords

  • Adrenergic blockers
  • Cardiogenic shock
  • Catecholamines
  • Pheochromocytoma
  • Surgery

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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  • Cite this

    Chatzizisis, Y. S., Ziakas, A., Feloukidis, C., Paramythiotis, D., Hadjimiltiades, S., Iliadis, A., Basdanis, G., & Styliadis, I. (2014). Pheochromocytoma crisis presenting with cardiogenic shock. Herz, 39(1), 156-160. https://doi.org/10.1007/s00059-013-3778-2