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一名成人出现左冠状动脉起源于肺动脉(ALCAPA)这一异常情况,同时右冠状动脉系统有两个分别来自主动脉的开口,这种情况不同寻常。

An unusual combination of an anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) and a right coronary artery system with two separate ostia from the aorta in an adult.

作者信息

Kats Yuliya, Solanki Pallavi, Waller Alfonso H, Maldjian Pierre D, Hamirani Kamran, Tsai Steve C, Dhruva Vivek, Klapholz Marc, Saric Muhamed

机构信息

Department of Medicine, New Jersey Medical School, Newark, New Jersey, USA.

出版信息

Echocardiography. 2010 Jan;27(1):E13-7. doi: 10.1111/j.1540-8175.2009.01040.x.

Abstract

We describe a patient with an infrequent combination of variants in both the right and the left coronary arterial ostia, namely a combination of two separate right coronary artery (RCA) ostia from the aorta, and an anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA). To our knowledge, such a combination has not been previously reported. Based on published statistics for individual variants, such a combination is expected to occur approximately once for every 500,000 to one million live births. ALCAPA and dual RCA anatomy was characterized in our patient by echocardiography, conventional angiography, and multidetector computed tomography before and after Takeuchi repair.

摘要

我们描述了一名患者,其左右冠状动脉开口存在罕见的变异组合,即两条独立的右冠状动脉(RCA)开口于主动脉,以及左冠状动脉起源于肺动脉(ALCAPA)的异常情况。据我们所知,这种组合此前尚未见报道。根据已发表的单个变异的统计数据,这种组合预计在每50万至100万活产中大约出现一次。在Takeuchi修复前后,通过超声心动图、传统血管造影和多排计算机断层扫描对我们患者的ALCAPA和双RCA解剖结构进行了特征描述。

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