一名患有 PA-VSD 的婴儿通过肺动脉瓣穿孔和右心室流出道支架植入术走向手术之路

E. Duras, E. Çilsal, Hacer Kamalı, Murat Sahin, A. Guzeltas
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引用次数: 0

摘要

肺动脉闭锁(PA)伴室间隔缺损(VSD)是一种罕见的先天性心脏病。肺动脉的血流由动脉导管未闭或大动脉-肺侧动脉(MAPCA)提供。为了维持肺动脉的血液供应,需要进行姑息性干预,以实现完全的手术修复。在本病例报告中,我们介绍了一名接受肺动脉瓣穿孔和右心室流出道(RVOT)支架植入术以替代全身-肺动脉分流术(SPS)的患者。十个月后,患者接受了手术修复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bridge to Surgery with Pulmonary Valve Perforation and Right Ventricular Outflow Tract Stenting in an Infant with PA-VSD
Pulmonary atresia (PA) with ventricular septal defect (VSD) is a rare congenital heart disease. Blood flow to pulmonary arteries is provided by patent ductus arteriosus or major aorto-pulmonary collateral arteries (MAPCAs). Palliative interventions are required to maintain the blood supply to the pulmonary arteries in order to achieve for the complete surgical repair. In this case report, we present a patient who underwent pulmonary valve perforation and right ventricular outflow tract (RVOT) stenting as an alternative to a systemic-pulmonary artery shunt (SPS). Subsequently, surgical repair was performed ten months later.
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