Abstract
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare coronary artery anomaly and double right coronary artery (RCA) is a very rare coronary anomaly. Because patients with ALCAPA usually die within 1 year of being born due to myocardial infarction (MI) and heart failure, ALPACA is very rarely seen in adults. Here, we report an extremely rare asymptomatic case of MI, presumably caused by ALCAPA and double RCA, and provide a review of the literature. This is the first reported case of coronary artery anomaly that had both ALCAPA and double RCA. Keywords: Coronary vessel anomalies; Myocardial infarction; Pulmonary artery ì¤ì¬ ë¨ì´: ê´ìë맥 기í; ì¬ê·¼ ê²½ìì¦; íë맥
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