作者: Paul J. Michaels , Jon A. Kobashigavpa , John S. Child , Michael C. Fishbein
DOI: 10.1053/HP.2000.6704
关键词:
摘要: Arrhythmogenic right ventricular dysplasia (ARVD) is a cause of heart failure and has been implicated in some cases sudden death young adults. It well known that large majority patients with ARVD have histological evidence suggestive inflammation. Here we report unique case chronic myocarditis limited to the ventricle side interventricular septum which presented clinically as ARVD. The fact sided can mimic genetic disease classic arrhythmogenic therapeutic implications for patient relatives.