先天性食管蹼：6例病例系列报告

Dysphagia lusoria: report of a series of six cases.

作者信息

Jalal Houda, El Idrissi Redouane, Azghari Amine, Ouazzani Laaziza, Benzzoubeir Nadia, Errabih Ikram, Krami Hayat, Ouazzani Houria, Bensaid Youness

机构信息

Gastroenterology unit B, Ibn Sina hospital, Souissi, Rabat, Morocco.

Vascular Surgery unit D, Ibn Sina hospital, Souissi, Rabat, Morocco.

出版信息

Clin Res Hepatol Gastroenterol. 2014 Jun;38(3):e45-9. doi: 10.1016/j.clinre.2013.02.015. Epub 2013 Apr 25.

DOI:10.1016/j.clinre.2013.02.015

PMID:23623447

Abstract

Dysphagia lusoria is a rare cause of organic dysphagia. This report describes a series of six patients admitted to our university hospital for dysphagia lusoria. Dysphagia was a constant feature in all our patients. Upper gastrointestinal endoscopy and a barium esophagram prompted the diagnosis, which was confirmed by angiography of the aortic arch showing an aberrant right subclavian artery in all cases. Treatment was surgical in all patients with good results.

摘要

先天性咽下困难是器质性咽下困难的罕见病因。本报告描述了6例因先天性咽下困难入住我院的患者。咽下困难是所有患者的常见症状。上消化道内镜检查和食管钡餐造影提示了诊断，主动脉弓血管造影证实所有病例均存在右锁骨下动脉异常，从而确诊。所有患者均接受了手术治疗，效果良好。