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酷似心包缺如的左心耳先天性巨大动脉瘤病例报告

Congenital giant aneurysm of the left atrial appendage mimicking pericardial absence case report.

作者信息

Kunishima T, Musha H, Yamamoto T, Aoyagi H, Kongoji K, Imai M, Ozawa A, So T, Nagashima J, Murayama M

机构信息

Department of Cardiology, Yokohama Seibu Hospital, St Marianna University, Japan.

出版信息

Jpn Circ J. 2001 Jan;65(1):56-9. doi: 10.1253/jcj.65.56.

Abstract

A 25-year-old man was found to have an abnormal cardiac contour on a chest radiograph, and was referred. Transesophageal echocardiography suggested herniation of the left atrial appendage (LAA) through a gap in the pericardium, and magnetic resonance imaging indicated congenital partial absence of the pericardium. Cardiac dysfunction was caused by compression from the enlarged left atrium and thrombi were thought to be present in the appendage, so surgery was performed. The intraoperative diagnosis was congenital LAA aneurysm. Although distinguishing between congenital LAA aneurysm and congenital absence of the pericardium is reported to be possible with magnetic resonance imaging, we were unable to so in this case.

摘要

一名25岁男性在胸部X线片上被发现心脏轮廓异常,随后前来就诊。经食管超声心动图提示左心耳(LAA)通过心包间隙疝出,磁共振成像显示先天性心包部分缺如。心脏功能障碍是由扩大的左心房压迫所致,且认为心耳内存在血栓,因此进行了手术。术中诊断为先天性LAA动脉瘤。尽管据报道磁共振成像可区分先天性LAA动脉瘤和先天性心包缺如,但在本病例中我们未能做到。

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