Adult type anomalous origin of the left coronary artery from the pulmonary artery

被引：0
|
作者：
Hallioglu, O [1 ]
Karagöz, T [1 ]
Çeliker, A [1 ]
机构：
[1] Hacettepe Univ, Fac Med, Pediat Cardiol Unit, Dept Pediat, TR-06100 Ankara, Turkey
来源：
TURKISH JOURNAL OF PEDIATRICS | 2004年 / 46卷 / 01期
关键词：
anomalous origin of the left coronary artery from the pulmonary artery; adult type; coronary anomalies;
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a clinical entity characterized by myocardial necrosis which becomes symptomatic shortly after birth; survival beyond infancy is uncommon because of severe left heart failure. To our knowledge, it is rare for an ALCAPA patient to survive to adulthood. Here we present a case of a 17-year-old girl with ALCAPA who was referred to our hospital because of palpitation and dyspnea.
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页码：92 / 94
页数：3
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