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成人先天性单叶主动脉瓣:综述与病例系列

Congenital unicuspid aortic valve in adults: Minireview and case series.

作者信息

Anwar Ashraf Mohammed, Alshawkani Hattan H, Albakri Ibrahim, Almatrafi Saleh J

机构信息

Department of Cardiology, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.

Department of Cardiology, Faculty of Medicine, Al-Azhar University, Cairo, Egypt.

出版信息

Ann Pediatr Cardiol. 2024 Jul-Aug;17(4):243-249. doi: 10.4103/apc.apc_153_24. Epub 2024 Nov 15.

Abstract

A unicuspid aortic valve (UAV) in adults is a very rare form of aortic valve (AV) malformation. UAV has two distinct subtypes, acommissural UAV and unicommissural, and can be differentiated by anatomical features, imaging modalities, and clinical presentation. With the development of significant AV lesion (s), surgical or transcatheter intervention will be required. The first part is a summarized review of UAV (anatomical features, clinical presentation, diagnostic modalities, and management). In the second part, we present a series of four patients diagnosed with UAV (3 unicommissural and 1 acommissural). The first case underwent balloon aortic valvuloplasty during childhood and surgical AV replacement later, with the progression to severe aortic stenosis (AS). The second case underwent a Ross procedure. The third and fourth cases were asymptomatic with moderate AS and mild-to-moderate AR and were kept on follow-up. In all the cases, transesophageal echocardiography confirmed the diagnosis of UAV with detailed morphological and functional assessment of AV.

摘要

成人单叶主动脉瓣(UAV)是一种非常罕见的主动脉瓣(AV)畸形形式。UAV有两种不同的亚型,无融合小叶型UAV和单融合小叶型,可通过解剖特征、成像方式和临床表现进行区分。随着严重AV病变的发展,将需要进行手术或经导管介入治疗。第一部分是对UAV(解剖特征、临床表现、诊断方式和治疗)的综述。在第二部分中,我们介绍了一系列四名被诊断为UAV的患者(3名单融合小叶型和1名无融合小叶型)。第一例在儿童期接受了球囊主动脉瓣成形术,后来进行了手术AV置换,病情进展为严重主动脉瓣狭窄(AS)。第二例接受了罗斯手术。第三例和第四例无症状,患有中度AS和轻度至中度AR,目前正在接受随访。在所有病例中,经食管超声心动图通过对AV进行详细的形态和功能评估证实了UAV的诊断。

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