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致心律失常性右室发育不良伴左心室广泛受累。

Arrhythmogenic right ventricular dysplasia with massive involvement of the left ventricle.

作者信息

Shoji T, Kaneko M, Onodera K, Konnno A, Hasegawa T, Ikeda T, Minase T, Uchiyama S, Iwamoto M

机构信息

Department of Emergency and Critical Care Medicine, Sapporo Medical College, Japan.

出版信息

Can J Cardiol. 1991 Sep;7(7):303-7.

PMID:1933637
Abstract

A 30-year-old male died suddenly after two years of clinically progressive episodes of recurrent ventricular tachycardia. In spite of recurrent episodes of palpitation, the patient had never shown signs or symptoms of heart failure before death. Post mortem examination revealed massive left ventricular involvement in addition to complete absence of myocardial tissue in the right ventricle, replaced by adipose tissue. This case illustrates that patients with arrhythmogenic right ventricular dysplasia may die of arrhythmia before failure of the left ventricle.

摘要

一名30岁男性在经历了两年临床症状逐渐加重的反复发作室性心动过速后突然死亡。尽管有心悸反复发作,但该患者在死亡前从未表现出心力衰竭的体征或症状。尸检显示除右心室完全没有心肌组织,被脂肪组织取代外,左心室也有大面积受累。该病例表明,致心律失常性右心室发育不良患者可能在左心室衰竭之前死于心律失常。

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