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胎儿罕见主动脉瓣畸形 1 例报告。

Unusual aortic valve anomaly in the fetus: a case report.

机构信息

Center of Fetal Cardiology, Policlinico San Donato IRCCS, Milan, Italy.

出版信息

Fetal Diagn Ther. 2012;32(3):221-4. doi: 10.1159/000341376. Epub 2012 Aug 24.

Abstract

Aortic valve anomalies in fetal life usually concern aortic valve stenosis, in severe forms associated to left ventricular impairment - endocardial fibroelastosis and mitral valve insufficiency. Isolated aortic regurgitation in utero is infrequent and is usually considered to be due to a rare anomaly: aorto-left ventricular tunnel. We describe an unusual case of fetal aortic valve anomaly with severe dysplasia, with a marked regurgitant flow through the aortic valve, passing in a retrograde way from the duct, associated with a marked left ventricular endocardial fibroelastosis and dysfunction, resulting in the fatal outcome of the case.

摘要

胎儿期主动脉瓣异常通常与主动脉瓣狭窄有关,严重者与左心室损害相关,如心内膜弹力纤维增生症和二尖瓣关闭不全。胎儿期单纯主动脉瓣反流较为少见,通常认为是一种罕见的异常:主动脉-左心室隧道。我们描述了一例罕见的胎儿主动脉瓣畸形病例,表现为严重发育不良,主动脉瓣有明显反流,经导管逆行通过,伴有明显的左心室心内膜弹力纤维增生症和功能障碍,导致该病例的致命结局。

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