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- Heiko Methe, Martin Hinterseer, Ute Wilbert-Lampen, Britt M Beckmann, Gerhard Steinbeck, and Stefan Kääb.
- Department of Cardiology, Ludwig-Maximilians-University, Munich, Germany. heiko.methe@med.uni-muenchen.de
- Hypertens. Res. 2007 Dec 1;30(12):1263-6.
AbstractPheochromocytoma is an infrequent secondary cause of arterial hypertension, often associated with paroxysmal headache, sweating, weight loss, and palpitations. Cardiovascular complications of pheochromocytoma include sudden death, heart failure due to toxic cardiomyopathy, and hypertensive encephalopathy. Here we report the case of a female with an acquired long-QT-syndrome as a rare complication of an extra-adrenal pheochromocytoma. Diagnosis was made after sotalol-induced Torsades de Pointes.
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