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Intraepithelial lymphocytes scores mimickers and challenges in diagnosing gluten-sensitive enteropathy (celiac disease)

机译:上皮内淋巴细胞评分轻笑和对面筋敏感肠病(celiac疾病)的诊断挑战

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摘要

The upper digestive tract is routinely scoped for several causes of malabsorption, and the number of duodenal biopsy specimens has increased notably in the last 10 years. Gluten-sensitive enteropathy (GSE) is an autoimmune disease, which shows an increasing prevalence worldwide and requires a joint clinico-pathological approach. The classical histopathology of GSE with partial or total villous blunting is well recognized, but the classification of GSE is not straightforward. Moreover, several mimickers of GSE with intraepithelial lymphocytosis have been identified in the last 20 years, with drug interactions and medical comorbidities adding to the conundrum. In this review, we report on the normal duodenal mucosa, the clinical presentation and laboratory diagnosis of GSE, the duodenal intraepithelial lymphocytes and immunophenotype of GSE-associated lymphocytes, the GSE mimickers, the differences “across oceans” among guidelines in diagnosing GSE, and the use of a synoptic report for reporting duodenal biopsies in both children and adults in the 21st century.
机译:上消化道通常是由吸收不良的几种原因引起的,在过去的十年中,十二指肠活检标本的数量显着增加。面筋敏感性肠病(GSE)是一种自身免疫性疾病,在全球范围内患病率正在上升,需要采取联合的临床病理方法。 GSE具有部分或全部绒毛变钝的经典组织病理学已得到公认,但GSE的分类并不简单。此外,在过去的20年中,已经发现一些GSE伴上皮内淋巴细胞增多的模仿者,药物相互作用和医学合并症增加了难题。在这篇综述中,我们报告了十二指肠粘膜正常,GSE的临床表现和实验室诊断,十二指肠上皮内淋巴细胞和GSE相关淋巴细胞的免疫表型,GSE mimickers,诊断GSE的指南之间“跨越大洋”的差异,以及概要报告用于报告21世纪儿童和成人的十二指肠活检。

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