Estenose sintomática da artéria subclávia direita aberrante

Luís Machado, Augusto Rocha e Silva, Armando Mansilha, José Teixeira
{"title":"Estenose sintomática da artéria subclávia direita aberrante","authors":"Luís Machado,&nbsp;Augusto Rocha e Silva,&nbsp;Armando Mansilha,&nbsp;José Teixeira","doi":"10.1016/j.ancv.2016.08.004","DOIUrl":null,"url":null,"abstract":"<div><p>The aberrant origin of the right subclavian artery, one of the most common anomalies of the aortic arch, occurs in approximately 0.5% to 1% of the population.</p><p>Usually asymptomatic, when symptoms are present they result from compression of the esophagus by the aberrant artery, aneurysmal degeneration or occlusive atherosclerotic disease. Occlusive symptoms are usually treated by surgical revascularization.</p><p>The authors present a case of a patient with a history of progressive claudication in the right upper limb, associated with dizziness. The imagiologic study revealed a stenosis of the right subclavian artery. The right subclavian artery had an aberrant course, behind the esophagus and trachea.</p><p>He underwent percutaneous treatment with primary stenting of the subclavian stenosis, without complications on the postoperative period. The patient still asymptomatic 4 years after the procedure.</p><p>Endovascular treatment has been used with excellent results in the treatment of occlusive disease of the subclavian artery, with few cases described of subclavian artery with aberrant origin.</p></div>","PeriodicalId":30341,"journal":{"name":"Angiologia e Cirurgia Vascular","volume":"12 4","pages":"Pages 275-278"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ancv.2016.08.004","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angiologia e Cirurgia Vascular","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1646706X16300611","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

The aberrant origin of the right subclavian artery, one of the most common anomalies of the aortic arch, occurs in approximately 0.5% to 1% of the population.

Usually asymptomatic, when symptoms are present they result from compression of the esophagus by the aberrant artery, aneurysmal degeneration or occlusive atherosclerotic disease. Occlusive symptoms are usually treated by surgical revascularization.

The authors present a case of a patient with a history of progressive claudication in the right upper limb, associated with dizziness. The imagiologic study revealed a stenosis of the right subclavian artery. The right subclavian artery had an aberrant course, behind the esophagus and trachea.

He underwent percutaneous treatment with primary stenting of the subclavian stenosis, without complications on the postoperative period. The patient still asymptomatic 4 years after the procedure.

Endovascular treatment has been used with excellent results in the treatment of occlusive disease of the subclavian artery, with few cases described of subclavian artery with aberrant origin.

异常右锁骨下动脉的症状性狭窄
右锁骨下动脉的异常起源是主动脉弓最常见的异常之一,约占人口的0.5%至1%。通常无症状,当出现症状时,是由异常动脉压迫食道、动脉瘤变性或闭塞性动脉粥样硬化疾病引起的。闭塞症状通常通过手术血运重建术治疗。作者提出了一例患者的历史进行性跛行在右上肢,与头晕相关。影像学检查显示右侧锁骨下动脉狭窄。右锁骨下动脉在食道和气管后的位置异常。他接受了经皮锁骨下狭窄的初步支架治疗,术后无并发症。术后4年患者仍无症状。血管内治疗已被用于治疗锁骨下动脉闭塞性疾病,具有良好的效果,很少有病例描述锁骨下动脉异常起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
审稿时长
14 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信