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食管、胃和十二指肠克罗恩病

Crohn's disease of esophagus, stomach and duodenum.

作者信息

Pimentel Andréa Maia, Rocha Raquel, Santana Genoile Oliveira

机构信息

Programa de Pós graduação em Medicina e Saúde, Universidade Federal da Bahia, Salvador 40110-060, Bahia, Brazil.

Departamento de Ciências da Nutrição, Universidade Federal da Bahia, Salvador 40110-060, Bahia, Brazil.

出版信息

World J Gastrointest Pharmacol Ther. 2019 Mar 7;10(2):35-49. doi: 10.4292/wjgpt.v10.i2.35.

Abstract

Crohn's disease with involvement of the esophagus, stomach and duodenum has a prevalence of 0.5% to 4% in symptomatic adult patients, but some studies have shown that these results may be underestimated, since upper gastrointestinal endoscopy is not performed routinely in the initial evaluation of the disease in adult patients, as it is in the pediatric population. In general, involvement of the upper gastrointestinal tract in Crohn's disease occurs concomitantly with involvement of the lower gastrointestinal tract. The diagnosis depends on clinical, endoscopic, histological and radiological evaluation. The presence of aphthoid ulcers, longitudinal ulcers, bamboo-joint-like appearance, stenoses and fistulas are endoscopic findings suggestive of the disease, and it is important to exclude the presence of infection. The primary histological findings, which facilitate the diagnosis, are the presence of a chronic inflammatory process with a predominance of lymphoplasmacytic cells and active focal gastritis. The presence of epithelioid granuloma, although less frequent, is highly suggestive of the disease in the absence of chronic granulomatous disease. Treatment should include the use of proton pump inhibitors associated with corticosteroids, immunomodulators and biological therapy according to the severity of the disease.

摘要

有食管、胃和十二指肠受累的克罗恩病在有症状的成年患者中的患病率为0.5%至4%,但一些研究表明这些结果可能被低估了,因为在成年患者疾病的初始评估中,不像在儿科人群中那样常规进行上消化道内镜检查。一般来说,克罗恩病中上消化道受累与下消化道受累同时发生。诊断取决于临床、内镜、组织学和放射学评估。阿弗他样溃疡、纵行溃疡、竹节样外观、狭窄和瘘管等内镜表现提示该病,排除感染的存在很重要。有助于诊断的主要组织学表现为以淋巴浆细胞为主的慢性炎症过程和活动性局灶性胃炎。上皮样肉芽肿的存在虽然较少见,但在没有慢性肉芽肿病的情况下高度提示该病。治疗应根据疾病的严重程度,包括使用与皮质类固醇、免疫调节剂和生物疗法联合的质子泵抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5757/6422852/3381f5a159e8/WJGPT-10-35-g001.jpg

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