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法洛四联症合并肺动脉瓣缺如综合征、右位主动脉弓及左肺动脉离断

Tetralogy of Fallot with absent pulmonary valve syndrome, right aortic arch, and disconnected left pulmonary artery.

作者信息

Solana-Gracia Ruth, Crossland David, Mitchell Leslie, Wren Christopher, Griselli Massimo

机构信息

Department of Paediatric Cardiology, Freeman Hospital, High Heaton, Newcastle upon Tyne, UK.

出版信息

World J Pediatr Congenit Heart Surg. 2013 Apr;4(2):206-9. doi: 10.1177/2150135112470960.

Abstract

We present a rare case of a two-week-old infant with tetralogy of Fallot , absent pulmonary valve syndrome , right aortic arch, and disconnected left pulmonary artery (LPA) whose origin was from ductal ligament adjacent to the left subclavian artery. One-stage surgical correction, including closure of ventricular septal defect (VSD), LPA reconstruction and reconnection to the pulmonary trunk, reduction in size of the right pulmonary artery (RPA), and right ventricular outflow tract reconstruction with valved conduit, was successfully performed with good clinical mid-term outcome.

摘要

我们报告了一例罕见的两周大婴儿,患有法洛四联症、肺动脉瓣缺如综合征、右位主动脉弓以及左肺动脉离断,其左肺动脉起源于左锁骨下动脉附近的动脉导管韧带。成功实施了一期手术矫正,包括室间隔缺损(VSD)闭合、左肺动脉重建并与肺动脉干重新连接、右肺动脉(RPA)缩窄以及使用带瓣管道进行右心室流出道重建,中期临床效果良好。

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