肥厚型心肌病患者的家族性完全性房室传导阻滞
[Familial complete atrioventricular block in patients with hypertrophic cardiomyopathy].
作者信息
Albanesi Filho F M, Ginefra P, Castier M B, da Rocha P J, de Albuquerque D C
机构信息
Hospital Universitário Pedro Ernesto, UERJ.
出版信息
Arq Bras Cardiol. 1992 Sep;59(3):209-13.
The association of spontaneous complete heart block and hypertrophic cardiomyopathy is rare. We have studied three patients of the same family, two brothers and one nephew, ages 19-41 years, with hypertrophic cardiomyopathy confirmed by hemodynamic and angiographic studies. All patients were treated with permanent cardiac pacemaker implant. They are asymptomatic, aging 33 to 55 years, with follow-up of 157 to 176 months after the onset of the heart block.
自发性完全性心脏传导阻滞与肥厚型心肌病的关联较为罕见。我们研究了同一家族的三名患者，两名兄弟和一名侄子，年龄在19至41岁之间，经血流动力学和血管造影研究确诊为肥厚型心肌病。所有患者均接受了永久性心脏起搏器植入治疗。他们目前无症状，年龄在33至55岁之间，自心脏传导阻滞发病后随访了157至176个月。
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