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完全性房室间隔缺损合并肺动脉闭锁伴主要体肺侧支动脉的一期确定性修复术。

One-stage definitive repair of complete atrioventricular septal defect and pulmonary atresia with major aortopulmonary collateral arteries.

作者信息

Ide Yujiro, Murata Masaya, Ito Hiroki, Sakamoto Kisaburo

机构信息

Department of Cardiovascular Surgery, Mt. Fuji Shizuoka Children's Hospital, Shizuoka, Japan.

出版信息

Interact Cardiovasc Thorac Surg. 2018 Feb 1;26(2):343-345. doi: 10.1093/icvts/ivx333.

Abstract

Pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries is considered the most severe end of the tetralogy of Fallot spectrum, whereas complete atrioventricular septal defect associated with tetralogy of Fallot is a rare congenital defect. However, the combination of pulmonary atresia, major aortopulmonary collateral artery and complete atrioventricular septal defect is extremely rare, and surgical repair has not been reported. We describe a successful, 1-stage correction in a 7-month-old boy with this condition, who had an additional complication of a single aortic outlet from the right ventricle and significant atrioventricular valve regurgitation.

摘要

肺动脉闭锁合并室间隔缺损及主要体肺侧支动脉被认为是法洛四联症谱系中最严重的类型,而合并法洛四联症的完全性房室间隔缺损是一种罕见的先天性缺陷。然而,肺动脉闭锁、主要体肺侧支动脉与完全性房室间隔缺损同时存在的情况极为罕见,且尚未见手术修复的报道。我们描述了一名患有此病症的7个月大男童成功接受一期矫治的病例,该患儿还伴有右心室单一主动脉出口及严重房室瓣反流的并发症。

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