Vol 20, No 1 (2013)
Case Reports
Published online: 2013-02-07
Long-term survivor diagnosed with arrhythmogenic right ventricular cardiomyopathy/dysplasia
DOI: 10.5603/CJ.2013.0013
Cardiol J 2013;20(1):83-86.
Abstract
The subject was a 70 year-old man who survived for 31 years after being diagnosed with right
ventricular cardiomyopathy, having undergone right ventricular (RV) aneurysmectomy at the
age of 39. His arrhythmia and syncopal attacks were effectively abolished after the original
aneurysmectomy. Although he frequently suffered from right heart failure, hemodialysis improved
his status. However, the patient died due to worsening anasarca caused by RV low
output syndrome. Autopsy results indicated extensive replacement of the RV myocardium with
fibrous and fatty tissues. This case suggests that patients with arrhythmogenic RV cardiomyopathy,
but without left ventricular abnormalities and rapid ventricular arrhythmia, have
a relatively favorable prognosis, although RV abnormalities may be progressive.
Keywords: right ventricular cardiomyopathyprognosisaneurysmectomy