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特发性颈段食管蹼:一例报告及文献综述

Idiopathic Cervical Esophageal Webs: A Case Report and Literature Review.

作者信息

Petrea Oana Cristina, Stanciu Carol, Muzica Cristina Maria, Sfarti Catalin Victor, Cojocariu Camelia, Girleanu Irina, Huiban Laura, Trifan Anca

机构信息

Department of Gastroenterology, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.

Institute of Gastroenterology and Hepatology, Iasi, Romania.

出版信息

Int J Gen Med. 2020 Nov 16;13:1123-1127. doi: 10.2147/IJGM.S278999. eCollection 2020.

Abstract

An esophageal web is a thin and smooth extension of normal esophageal tissue consisting of mucosa and submucosa that can occur anywhere along the length of the esophagus but is typically located in the cervical segment. The webs can be congenital or acquired, commonly associated with Plummer-Vinson syndrome and rarely with celiac disease, dermatological disorders or graft-versus-host disease. A 54-year-old man was referred to our hospital with a history of high non-progressive dysphagia to solid food, meat impaction and weight loss over last ten months. His medical history and family history were unremarkable nor was the physical examination. Complete blood count and basic biochemical tests were normal. Antigliadin and antiendomysial antibodies for celiac disease were negative. Barium swallow esophagography and upper endoscopy detected cervical esophageal webs. The treatment consisted of endoscopic balloon dilation. The patient's dysphagia resolved shortly after dilation, and the endoscope passed easily through the esophagus showing normal esophageal, gastric and duodenal mucosa. This report is consistent with a case of esophageal webs rarely documented in males and that is not related with common causes like Plummer-Vinson syndrome. Thus, the pathogenesis and treatment of esophageal webs are evolving.

摘要

食管蹼是由黏膜和黏膜下层组成的正常食管组织的薄而光滑的延伸部分,可出现在食管全长的任何部位,但通常位于颈段。食管蹼可分为先天性或后天性,通常与普卢默 - 文森综合征相关,很少与乳糜泻、皮肤病或移植物抗宿主病有关。一名54岁男性因过去十个月来有进食固体食物时进行性吞咽困难、肉团嵌塞和体重减轻的病史而被转诊至我院。他的病史和家族史无异常,体格检查也无异常。全血细胞计数和基本生化检查均正常。检测乳糜泻的抗麦胶蛋白和抗肌内膜抗体均为阴性。吞钡食管造影和上消化道内镜检查发现颈段食管蹼。治疗方法为内镜下球囊扩张。扩张后患者的吞咽困难很快缓解,内镜可轻松通过食管,显示食管、胃和十二指肠黏膜正常。本报告符合一例男性罕见的食管蹼病例,且与普卢默 - 文森综合征等常见病因无关。因此,食管蹼的发病机制和治疗方法正在不断发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c946/7679475/4a62144eb5f7/IJGM-13-1123-g0001.jpg

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