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Torsades de Pointes: a rare complication of an extra-adrenal pheochromocytoma.

Abstract
Pheochromocytoma 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.
AuthorsHeiko Methe, Martin Hinterseer, Ute Wilbert-Lampen, Britt M Beckmann, Gerhard Steinbeck, Stefan Kääb
JournalHypertension research : official journal of the Japanese Society of Hypertension (Hypertens Res) Vol. 30 Issue 12 Pg. 1263-6 (Dec 2007) ISSN: 0916-9636 [Print] England
PMID18344633 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Anti-Arrhythmia Agents
  • Sotalol
Topics
  • Adrenal Gland Neoplasms (complications)
  • Adult
  • Anti-Arrhythmia Agents (adverse effects)
  • Electrocardiography
  • Female
  • Humans
  • Pheochromocytoma (complications)
  • Risk Factors
  • Sotalol (adverse effects)
  • Torsades de Pointes (chemically induced, diagnosis, etiology)

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