Arrhythmogenic right ventricular dysplasia: clinical features, diagnostic techniques, and current management.
Arrhythmogenic right ventricular dysplasia: clinical features, diagnostic techniques, and current management.
复制标题
致心律失常性右心室发育不良:临床特征、诊断技术和当前治疗。
DOI:
10.1016/0002-8703(82)90282-4
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发表时间:
1982
影响因子:
4.8
通讯作者:
Robert J. Hall
中科院分区:
文献类型:
--
作者:
Peter A. Rossi;Peter A. Rossi;Ali Massumi;Ali Massumi;Paul C. Gillette;Paul C. Gillette;Robert J. Hall;Robert J. Hall
In 1978, Frank et al1 reported four cases of recurrent ventricular tachycardia (VT) associated with an isolated right ventricular (RV) cardiomyopathy. These patients had been initially evaluated because of recurrent VT occurring in the absence of previously known heart disease. Electrophysiologic studies (EPS) demonstrated VT originating in the RV that was inducible with programmed stimulation. During sinus rhythm, decreased conduction velocity through the RV myocardium was observed. Angiography revealed hypokinesis of the RV with localized dyskinetic zones. They named the syndrome arrhythmogenic right ventricular dysplasia (ARVD). Since their initial description, 34 more cases have been reported in adults2 As exemplified by the patient described herein, the purpose of the present report is to delineate the clinical features of this newly identified entity with emphasis on the techniques of diagnosis and the current management of ARVD.
影响因子:
2.4
作者:
Prystowsky,EN;Heger,JJ;Lloyd,EA;Zipes,DP
通讯作者:
Zipes,DP