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陶西格-宾氏畸形:经肺动脉闭合室间隔缺损的完全修复术。

Taussig-Bing anomaly: total repair with closure of ventricular septal defect through the pulmonary artery.

作者信息

Ottino G, Kugler J D, McNamara D G, Hallman G L

出版信息

Ann Thorac Surg. 1980 Feb;29(2):170-6. doi: 10.1016/s0003-4975(10)61658-x.

Abstract

Total surgical repair of a Taussig-Bing malformation in an 8-year-old boy was accomplished successfully after previous palliative procedures. The child had undergone a Rashkind septostomy when he was 10 days old, banding of the pulmonary artery and division of a patent ductus arteriosus when he was 2 weeks old, and a Blalock-Hanlon septectomy when he was 1 year old. Complete repair involved patching the ventricular septal defect (VSD), debanding and patching the pulmonary artery, and rerouting the venous return by performing a Mustard procedure. Because of its high location, the VSD could not be reached properly through the tricuspid valve and was approached through the pulmonary arteriotomy. Excellent exposure was obtained by retracting the pulmonary valve, and patch closure of the defect was achieved without difficulties. We believe this approach to the VSD is preferable because no incision is necessary in the right ventricle. This is important since the right ventricle becomes the systemic ventricle after the Mustard operation.

摘要

一名8岁男孩在先前进行姑息手术后成功完成了陶西格-宾畸形的全手术修复。该患儿10日龄时接受了拉什金德房间隔造口术,2周龄时接受了肺动脉束带术和动脉导管未闭结扎术,1岁时接受了布莱洛克-汉隆房间隔切除术。完全修复包括修补室间隔缺损(VSD)、解除肺动脉束带并进行修补,以及通过实施马斯塔德手术重新引导静脉回流。由于室间隔缺损位置较高,无法通过三尖瓣适当到达,因此通过肺动脉切开术进行处理。通过牵拉肺动脉瓣获得了极佳的视野,缺损的补片闭合顺利完成。我们认为这种处理室间隔缺损的方法更可取,因为无需在右心室做切口。这很重要,因为在马斯塔德手术后右心室成为体循环心室。

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