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非法洛四联症型肺动脉瓣缺如综合征患者的外科治疗

Surgical Management of a Patient With Non-Fallot-Type Absent Pulmonary Valve Syndrome.

作者信息

Breithaupt Jason J, Fraser Charles, Leahy Ryan, Mejak Brian, Burkett Dale, Albertz Megan, Kim John, Stone Matthew L

机构信息

Department of Surgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO, USA.

Section of Congenital Heart Surgery, Heart Institute, Children's Hospital Colorado, University of Colorado Denver | Anschutz Medical Campus, Aurora, CO, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2025 Sep;16(5):694-696. doi: 10.1177/21501351251327214. Epub 2025 Apr 15.

DOI:10.1177/21501351251327214
PMID:40233133
Abstract

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.

摘要

我们描述了一名婴儿的临床表现及治疗情况,该婴儿具有一系列独特的心脏结构异常,包括巨大的动脉导管未闭、严重的肺动脉瓣功能不全、三尖瓣发育不全,以及由此导致的右心室显著扩张和肥厚,室间隔完整。手术包括动脉导管结扎及切断、主动脉弓同种异体补片扩大成形、改良布莱洛克 - 陶西格 - 托马斯分流术、右心室到肺动脉同种异体移植术以及房间隔切除术。

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Surgical Management of a Patient With Non-Fallot-Type Absent Pulmonary Valve Syndrome.非法洛四联症型肺动脉瓣缺如综合征患者的外科治疗
World J Pediatr Congenit Heart Surg. 2025 Sep;16(5):694-696. doi: 10.1177/21501351251327214. Epub 2025 Apr 15.
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