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一名患有先天性矫正型大动脉转位、右主动脉弓发育不全和埃布斯坦畸形的新生儿的手术治疗

Surgical management of a neonate with congenitally corrected transposition of the great vessels, hypoplastic right aortic arch, and Ebstein anomaly.

作者信息

Filippelli Sergio, Perri Gianluigi, Kirk Richard, Hasan Asif, Griselli Massimo

机构信息

Paediatric Cardiothoracic Surgery Department, Freeman Hospital, Newcastle Upon Tyne, United Kingdom.

出版信息

J Card Surg. 2013 Nov;28(6):764-6. doi: 10.1111/jocs.12200. Epub 2013 Aug 15.

Abstract

We report a neonate with a primary diagnosis of congenitally corrected transposition (ccTGA) of the great vessels, hypoplastic right aortic arch, and a severely regurgitant Ebstein tricuspid valve (TV). During the fetal period, she was listed for heart transplantation, and two weeks after birth due to a deterioration of her general condition, we performed a Norwood-Sano modified procedure. After 58 days a donor heart became available and the baby successfully received a orthotopic heart transplantation.

摘要

我们报告了一名新生儿,其初步诊断为大动脉先天性矫正型转位(ccTGA)、右主动脉弓发育不全以及Ebstein三尖瓣(TV)严重反流。在胎儿期,她被列入心脏移植名单,出生两周后,由于全身状况恶化,我们为她实施了诺伍德-佐野改良手术。58天后获得了供体心脏,婴儿成功接受了原位心脏移植。

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