Acute heart failure with incidentally found cystic adrenal mass

Salman Zahoor Bhat, Roberto Salvatori, Amir H. Hamrahian, Yubo Wu, Misop Han

Research output: Contribution to journalArticlepeer-review

Abstract

Pheochromocytomas are rare adrenal tumors characterized by excessive catecholamine secretion. Symptoms and signs associated with pheochromocytomas are usually intermittent and chronic but can rarely develop into life-threatening crises. We describe a case of acute severe congestive heart failure in a previously healthy female, who recovered rapidly (4 days after admission) with acute medical therapy. The etiology on evaluation was a spontaneous bleed in a previously undiagnosed pheochromocytoma, resulting in a pheochromocytoma crisis and transient stress cardiomyopathy, followed by quick recovery of cardiac function. Our aim is to describe pheochromocytoma as a rare cause of stress cardiomyopathy. We discuss the evaluation of pheochromocytoma during critical illness and triggers/treatment strategies for pheochromocytoma crises.

Original languageEnglish (US)
Article number23-0051
JournalEndocrinology, Diabetes and Metabolism Case Reports
Volume2023
Issue number4
DOIs
StatePublished - Oct 2023

Keywords

  • 2023
  • Adrenal
  • Adult
  • Cardiovascular endocrinology
  • Female
  • October
  • Unique/unexpected symptoms or presentations of a disease
  • United States
  • White

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism

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