| Literature DB >> 7554549 |
A S Nanda1, A Feldman, C S Liang.
Abstract
Pheochromocytoma is a rare neuroendocrine tumor. We report a case of pheochromocytoma-induced cardiomyopathy in an 18-year old white female. A review of the literature indicated that this is the most dramatic reversal of pheochromocytoma cardiomyopathy reported. With aggressive medical management, there was complete recovery of the hemodynamic, echocardiographic, and electrocardiographic abnormalities within 14 days. This case emphasizes the importance of aggressive and appropriate medical therapy in pheochromocytoma heart disease.Entities:
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Year: 1995 PMID: 7554549 DOI: 10.1002/clc.4960180712
Source DB: PubMed Journal: Clin Cardiol ISSN: 0160-9289 Impact factor: 2.882