非法洛特型缺瓣肺动脉综合征1例的外科治疗。

Jason J Breithaupt, Charles Fraser, Ryan Leahy, Brian Mejak, Dale Burkett, Megan Albertz, John Kim, Matthew L Stone
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引用次数: 0

摘要

我们描述了一个具有大量动脉导管未闭,肺动脉瓣严重不足,三尖瓣发育不全,导致右心室深度扩张和肥厚,室间隔完整的婴儿的表现和处理。手术包括导管结扎和分割、主动脉弓同种移植物补片增强、改良的Blalock-Taussig-Thomas分流置入术、右心室至肺动脉同种移植物置入术和房间隔切除术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgical Management of a Patient With Non-Fallot-Type Absent Pulmonary Valve Syndrome.

We describe the presentation and management of an infant with the unique constellation of a massive patent ductus arteriosus, severely insufficient pulmonary valve, hypoplastic tricuspid valve, and a resultant profoundly dilated and hypertrophic right ventricle with intact interventricular septum. Surgery consisted of ductal ligation and division, homograft patch augmentation of the aortic arch, modified Blalock-Taussig-Thomas shunt placement, right ventricle-to-pulmonary artery homograft placement, and atrial septectomy.

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