Anomalous left coronary artery from the pulmonary arteryin an adult
John D Vossler1, Daniel W Entrikin, Michael D Quartermain
1Division of Cardiothoracic Surgery, Wake Forest Baptist Health, Winston-Salem, North Carolina, USA.
Abstract:
Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart defect that usually presents before the age of 1 year. Several surgical options exist for the correction of ALCAPA; however, debate continues regarding the optimal repair technique in adult populations. We report the case of successful surgical repair of ALCAPA with a direct aortic implantation technique in a 44-year-old mother of 4 children.
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