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一名年轻突尼斯男子因贫血而被诊断出患有胶原性胃炎。

Anemia revealing a collagenous gastritis in a young Tunisian man.

作者信息

Akkari Imen, Skandrani Karim, Abdelkader Atef Ben, Mrabet Soumaya, Jazia Elhem Ben

机构信息

Gastroenterology Department, Farhat Hached Hospital, Sousse, Tunisia.

Anatomopathology Department, Farhat Hached Hospital, Sousse, Tunisia.

出版信息

Pan Afr Med J. 2018 Jul 26;30:231. doi: 10.11604/pamj.2018.30.231.12981. eCollection 2018.

Abstract

Collagenous gastritis is a rare entity, characterized by the deposition of a subepithelial collagenous band with an inflammatory infiltrate in the mucosa. We report the first Tunisian case revealed by severe anemia. Lesions were limited to the stomach and remained unchanged on 3 series biopsies during a 24 month follow up despite treatment with corticosteroids. The cause of the disease remains unknown; our findings suggest that lesions of collagenous gastritis may result from a local immune process.

摘要

胶原性胃炎是一种罕见的疾病,其特征是黏膜下有一条胶原带沉积,并伴有炎症浸润。我们报告了突尼斯首例因严重贫血而发现的病例。病变局限于胃部,在24个月的随访期间,尽管使用了皮质类固醇进行治疗,但3次系列活检结果显示病变并无变化。该病的病因仍然不明;我们的研究结果表明,胶原性胃炎的病变可能是由局部免疫过程引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d7a/6295307/c7ec101d22fe/PAMJ-30-231-g001.jpg

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