Aberrant Right Subclavian Artery: Cadaver Case Report

Jason A. Kopp, Ahmad Irshaid, Justin N. Baker, J. Fitzsimmons, Judith C. Lin
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引用次数: 1

Abstract

While examining the anatomy of a cadaver in a medical school gross anatomy course, an aortic arch anomaly was discovered. This variant is consistent with an aberrant right subclavian artery (ARSA). In this variant the right subclavian artery branches from the most distal part of the aortic arch and runs both retrotracheal and retroesophageal as it courses to the right shoulder. This variant is a result of aberrant development of the aortic arch and may include presenting symptoms such as dysphagia and shortness of breath, if any at all. Additional to the ARSA exists a common bicarotid trunk and a direct branching of the left vertebral artery from the aortic arch, both of which are rare anomalies. The cadaver’s medical history includes dysphagia and stretched esophagus, although the severity is unknown. This case report draws attention to these rare anatomical anomalies and includes a discussion of the most common clinical presentation, and surgical implications of an aberrant right subclavian artery anomaly.
右锁骨下动脉异常:尸体病例报告
在一所医学院的大体解剖课上,在检查一具尸体的解剖结构时,发现了一个主动脉弓异常。这种变异与右锁骨下动脉(ARSA)异常一致。在这种情况下,右锁骨下动脉从主动脉弓的最远端分支,并在气管后和食管后向右肩延伸。这种变异是主动脉弓异常发育的结果,可能包括吞咽困难和呼吸短促等症状,如果有的话。除了ARSA外,还有一个共同的二颈动脉干和左椎动脉从主动脉弓直接分支,这两个都是罕见的异常。尸体的病史包括吞咽困难和食管拉伸,但严重程度未知。本病例报告关注这些罕见的解剖异常,并讨论了最常见的临床表现,以及异常的右锁骨下动脉异常的手术意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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