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主动脉心室通道:主动脉瓣反流和心肌致密化不全——修复术后常见的晚期关联病变。

Aorto-ventricular tunnel: Aortic regurgitation and noncompaction cardiomyopathy - Common late associations after repair.

作者信息

Martin de Miguel Irene, Egbe Alexander C, Connolly Heidi M, O'Leary Patrick W, Miranda William R

机构信息

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN 55905, USA.

Department of Pediatric and Adolescent Medicine/Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Int J Cardiol Congenit Heart Dis. 2022 Apr 1;8:100367. doi: 10.1016/j.ijcchd.2022.100367. eCollection 2022 Jun.

Abstract

Aorto-ventricular tunnels are rare, congenital extracardiac connections arising from the tubular ascending aorta, above the sinotubular junction, which communicate directly with the ventricular cavity. We present long-term follow-up in a series of five adults undergoing pediatric repair and describe the cardiovascular features and outcomes. Significant aortic regurgitation, ascending aortic aneurysm and left ventricular noncompaction were found to be highly prevalent, emphasizing the need for ongoing surveillance following repair of this anomaly.

摘要

主动脉-心室通道罕见,是一种先天性心外连接,起源于管状升主动脉,位于窦管交界处上方,直接与心室腔相通。我们对一组5例接受小儿修复术的成人进行了长期随访,并描述了其心血管特征及结果。发现严重主动脉瓣反流、升主动脉瘤和左心室心肌致密化不全非常普遍,强调了对这种异常修复后进行持续监测的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d9/11657155/b6b7b1a50f0e/gr1.jpg

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