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Abnormal single coronary artery from pulmonary artery (ASCAPA) associated with ventricular septal defect and pulmonary valve stenosis in young infant presented with heart failure: Case report

机译:肺动脉(ASCAPA)异常冠状动脉(ASCAPA)与心室间隔缺损和心力衰竭患者患有心力衰竭的年轻婴儿的肺瓣狭窄:案例报告

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摘要

Abnormal single coronary artery from pulmonary artery (ASCAPA) is a very rare anomaly; it is rarer than anomalous left coronary artery from pulmonary artery (ALCAPA). The incidence of ASCAPA is unknown because of little number of reported cases; it may be isolated or associated with other congenital heart diseases and is usually associated with significant myocardial ischemia and dysfunction timed with the physiological decrease of pulmonary vascular resistance (PVR) after birth. We are reporting a case of ASCAPA associated with peri-membranous ventricular septal (VSD) defect and valvular pulmonary stenosis in an infant that presented with heart failure.
机译:来自肺动脉(Ascapa)的异常冠状动脉(ascapa)是一个非常罕见的异常; 肺动脉(Alcapa)的异常左冠状动脉稀有。 由于少数报道的病例,阿昔巴的发病率未知; 它可以与其他先天性心脏病分离或相关,并且通常与出生后肺血管抗性(PVR)的生理降低相比,与显着的心肌缺血和功能障碍有关。 我们报告了与患有心力衰竭的婴儿患有肝脏室间隔(VSD)缺陷和瓣膜肺狭窄相关的ASCAPA的案例。

著录项

  • 来源
    《Progress in pediatric cardiology》 |2019年第2019期|共1页
  • 作者

    Gaser Abdelmohsen;

  • 作者单位

    Pediatric Cardiology Division Department of Pediatrics Cairo University Cairo Egypt;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 儿科学;
  • 关键词

  • 入库时间 2022-08-20 06:37:41

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