家族性扩张型心肌病合并左心室动脉瘤。

Familial dilated cardiomyopathy complicated by left ventricular aneurysm.

作者信息

Hirakawa Y, Koyanagi S, Matsumoto T, Itaya R, Takeshita A, Nakamura M

机构信息

Research Institute of Angiocardiology and Cardiovascular Clinic, Kyushu University School of Medicine, Fukuoka, Japan.

出版信息

Jpn Heart J. 1990 Mar;31(2):245-9. doi: 10.1536/ihj.31.245.

DOI:10.1536/ihj.31.245

PMID:2355459

Abstract

Two siblings presented with symptoms of left ventricular dysfunction and ventricular arrhythmias. Echocardiography and left ventriculography revealed dilatation, diffuse hypokinesis and apical aneurysm of the left ventricle in both cases. Myocardial infarction was unlikely by history and examinations. We diagnosed them as cases of familial dilated cardiomyopathy complicated by left ventricular aneurysm.

摘要

两名兄弟姐妹出现左心室功能障碍和室性心律失常症状。超声心动图和左心室造影显示，两例患者均存在左心室扩张、弥漫性运动减弱和心尖部室壁瘤。根据病史和检查结果，心肌梗死的可能性不大。我们将他们诊断为家族性扩张型心肌病并发左心室室壁瘤病例。