Department of Cardiac Surgery, Montreal Heart Institute, Montreal, Québec, Canada.
Department of Cardiology, Montreal Heart Institute, Montreal, Québec, Canada.
Can J Cardiol. 2016 Dec;32(12):1576.e1-1576.e3. doi: 10.1016/j.cjca.2015.12.017. Epub 2015 Dec 28.
Late presentation of an anomalous left coronary artery from the pulmonary artery (ALCAPA) is uncommon because patients rarely survive past infancy. We present a case of symptomatic ALCAPA associated with decreased myocardial contractility in a 68-year-old woman. The patient underwent reimplantation of the left coronary artery in the aortic root.
左冠状动脉异常起源于肺动脉(ALCAPA)的迟发表现较为少见,因为此类患者很少能存活到婴儿期以后。我们报告了一例与心肌收缩力降低相关的有症状性 ALCAPA 病例,患者为 68 岁女性。该患者接受了左冠状动脉在主动脉根部的再植入手术。