Ergenoglu Mehmet U, Yerebakan Halit, Ozveren Olcay, Koner Ozge, Kalangos Afksendiyos, Demirsoy Ergun
Department of Cardiovascular Surgery, Yeditepe University Hospital, Istanbul, Turkey.
Heart Surg Forum. 2011 Oct;14(5):E326-7. doi: 10.1532/HSF98.20111046.
Congenitally corrected transposition of the great arteries, which is characterized by atrioventricular and ventriculoarterial discordance, is a rare congenital heart disease. Most of the cases are diagnosed in childhood, owing to associated cardiac anomalies, such as ventricular septal defect, pulmonary stenosis or pulmonary atresia, and Ebstein-like malformation of the tricuspid valve. We present a patient with congenitally corrected transposition of the great arteries who underwent surgical replacement of the tricuspid valve with a bioprosthesis and reconstruction of the left ventricular outflow tract with bovine conduit.
先天性矫正型大动脉转位是一种罕见的先天性心脏病，其特征为房室和心室动脉不一致。由于存在相关心脏异常，如室间隔缺损、肺动脉狭窄或肺动脉闭锁以及三尖瓣埃布斯坦样畸形，大多数病例在儿童期被诊断出来。我们报告一例先天性矫正型大动脉转位患者，该患者接受了生物瓣置换三尖瓣及用牛心包补片重建左心室流出道的手术。
