A case of aberrant right subclavian artery with the development of Bayford–Autenrieth dysphagia

A. G. Alekseev, A. V. Maksimov, N. P. Chizhikov, A. A. Poletaeva, D. A. Sokolov, A. A. Shevchenko
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Abstract

   Developmental anomalies of the aortic arch and its large vessels can be accompanied not only by hemodynamic disorders, but also affect the functions of internal organs. This report analyzes the case of an autopsy finding of the right aberrant subclavian artery in an 80-year-old patient, which was clinically manifested by the development of dysphagia and cachexia. An autopsy revealed the absence of the brachiocephalic trunk, which normally originates from the arch of the authors, as well as an abnormal origin of the right subclavian artery from the posterior surface of the aortic arch, 1,1 cm to the left and distal to the orifice of the left subclavian artery. The proximal segment of the abnormal vessel, up to 1,0 cm in diameter, was located between the spinal column and the esophagus, leading to its compression.
右锁骨下动脉异常伴bayford - autenriths吞咽困难1例
主动脉弓及其大血管发育异常不仅可伴有血流动力学障碍,还可影响内脏器官的功能。本文报告一例80岁患者尸检发现锁骨下动脉右侧异常,临床表现为吞咽困难和恶病质的发展。尸检显示头臂干的缺失,通常起源于作者的弓,以及右锁骨下动脉的异常起源,从主动脉弓的后表面,左1.1厘米和远端的左锁骨下动脉的开口。异常血管的近段,直径达1 0 cm,位于脊柱和食道之间,导致其受压。
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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