[手术治疗吞咽困难]。

Q3 Medicine
Revue medicale de Liege Pub Date : 2023-07-01
Natacha Mawait, Arnaud Kerzmann, Quentin Desiron, Denis Henroteaux, Laurie Stiennon, Jean Olivier Defraigne
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引用次数: 0

摘要

右锁骨下动脉异常,也称为阔动脉,是主动脉弓最常见的先天性异常(患病率为0.5% - 1.8%)。21三体患者的患病率更高(35%)。它起源于主动脉弓在其他三个主动脉上干之后。它可能与其他心血管异常有关。在超过80%的病例中,异常动脉位于食道后方。通常是无症状的。有时它与40岁以后的症状有关,多见于女性:吞咽困难(吞咽困难),呼吸困难或咳嗽。诊断是通过计算机断层扫描或磁共振成像。当有症状时,需要对食道进行钡剂造影。通过异常血管转位的手术治疗仅适用于有症状的患者。我们报告的情况下,50岁的妇女吞咽困难的治疗异常右锁骨下动脉转位到右颈总动脉通过颈椎入路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Dysphagia lusoria treated by surgery].

Aberrant right subclavian artery, also called arteria lusoria, is the most common congenital anomaly of the aortic arch (prevalence 0,5-1.8 %). Patients with trisomy 21 have a higher prevalence (35 %). It takes its origin from the aortic arch after the three others supra-aortic trunks. It may be associated with other cardiovascular anomalies. In more than 80 % of cases, the aberrant artery is positioned behind the oesophagus. It is often asymptomatic. Sometimes it is associated with symptoms after the age of 40 years old, more often among women: dysphagia (dysphagia lusoria), dyspnoea or cough. Diagnosis is made by computed tomography or magnetic resonance imaging. When it is symptomatic, a barium contrast radiography of the oesophagus is indicated. Surgical treatment by transposition of the aberrant vessel is performed only for symptomatic patients. We report the case of a 50-year-old woman with dysphagia lusoria treated by transposition of the aberrant right subclavian artery into the right common carotid through a cervical approach.

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来源期刊
Revue medicale de Liege
Revue medicale de Liege Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
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0
期刊介绍: The Medical Review of Liege is a tool for continuous medical training being addressed to students, general practitioners, and specialists
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