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一例罕见的颈主动脉弓中断合并降主动脉长节段缩窄病例。

An unusual case of interrupted cervical aortic arch associated with long segment coarctation of the descending thoracic aorta.

作者信息

Dey Mousam, Garg Naveen, Kumar Sunil

机构信息

1Department of Radiology,Sanjay Gandhi Post Graduate Institute of Medical Sciences,Lucknow,India.

2Department of Cardiology,Sanjay Gandhi Post Graduate Institute of Medical Sciences,Lucknow,India.

出版信息

Cardiol Young. 2018 Apr;28(4):592-594. doi: 10.1017/S1047951117001913. Epub 2018 Feb 9.

Abstract

Interrupted aortic arch is a rare congenital anomaly in newborns and infants and is commonly associated with other cardiovascular anomalies. Here, we report an unusual case of type A interrupted cervical aortic arch associated with long segment coarctation of the descending thoracic aorta. Patent ductus arteriosus reconstituted the descending thoracic aorta. Proximal segments of the left common carotid and left subclavian arteries were atretic. Echocardiography-gated multidetector CT angiography not only identified the type of aortic arch interruption in the neonate but also delineated the exact anatomical details.

摘要

主动脉弓中断是新生儿和婴儿中一种罕见的先天性异常,通常与其他心血管异常相关。在此,我们报告一例不寻常的A型颈段主动脉弓中断病例,该病例伴有胸降主动脉长段缩窄。动脉导管未闭重建了胸降主动脉。左颈总动脉和左锁骨下动脉近端节段闭锁。超声心动图门控多排螺旋CT血管造影不仅确定了新生儿主动脉弓中断的类型,还描绘了确切的解剖细节。

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