Nanda A S, Feldman A, Liang C S
Department of Internal Medicine, University of Rochester School of Medicine and Dentistry, New York, USA.
Clin Cardiol. 1995 Jul;18(7):421-3. doi: 10.1002/clc.4960180712.
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.
嗜铬细胞瘤是一种罕见的神经内分泌肿瘤。我们报告一例18岁白人女性因嗜铬细胞瘤诱发心肌病的病例。文献回顾表明,这是所报道的嗜铬细胞瘤心肌病最显著的逆转情况。通过积极的药物治疗,血流动力学、超声心动图及心电图异常在14天内完全恢复。该病例强调了积极且恰当的药物治疗在嗜铬细胞瘤性心脏病中的重要性。