...
首页> 外文期刊>Journal of cardiac surgery. >ALCAPA in an adult with preserved left ventricular function.
【24h】

ALCAPA in an adult with preserved left ventricular function.

机译:成年人左心功能保留的ALCAPA。

获取原文
获取原文并翻译 | 示例
           

摘要

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is the most common congenital coronary artery defect. Left uncorrected, nearly 90% of patients will die within one year. Without surgical repair, surviving patients are subjected to risks of myocardial ischemia with global cardiomyopathy, chronic mitral regurgitation, and sudden death. We report a case of ALCAPA in a 23-year-old female with completely preserved left ventricular function. This article reviews the mechanism of this unusual presentation as well as the therapeutic options for adults presenting with ALCAPA.
机译:左冠状动脉异常起源于肺动脉(ALCAPA)是最常见的先天性冠状动脉缺损。如果不加以纠正,将近90%的患者会在一年内死亡。如果不进行手术修复,幸存的患者将面临发生心肌缺血,整体性心肌病,慢性二尖瓣关闭不全和猝死的危险。我们报告了一名23岁女性,完全保留左心室功能的ALCAPA病例。本文回顾了这种异常表现的机制,以及成年人ALCAPA的治疗选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号