Suppr超能文献

难治性乳糜泻的最新进展:综述

Recent advances in refractory coeliac disease: a review.

作者信息

Ho-Yen C, Chang F, van der Walt J, Mitchell T, Ciclitira P

机构信息

Department of Histopathology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

出版信息

Histopathology. 2009 Jun;54(7):783-95. doi: 10.1111/j.1365-2559.2008.03112.x. Epub 2009 Aug 12.

Abstract

Coeliac disease (CD) is an immune-mediated disease of the small intestine caused by intolerance to gluten. Removal of gluten from the diet results in a return to normal health for the majority of patients. A significant proportion of patients do not respond to a gluten-free diet and are considered to be suffering from refractory coeliac disease (RCD). Two types of RCD are now recognized: type 1 RCD is characterized by a polyclonal population of intraepithelial lymphocytes (IELs) with a normal immunophenotype, and type 2 RCD shows monoclonal IELs with an aberrant immunoprofile. Patients with RCD have a high risk of complications such as ulcerative jejunitis (UJ) and enteropathy-type T-cell lymphoma (ETTL). RCD2 may represent an early stage in the development of overt lymphoma. The diagnosis of RCD, therefore, has important implications, but remains a challenging area. In this paper we review the latest developments in RCD, including the diagnostic approach and a discussion of the key clinical, histological, immunohistochemical and molecular features of RCD and its complications.

摘要

乳糜泻(CD)是一种由对麸质不耐受引起的小肠免疫介导性疾病。大多数患者通过从饮食中去除麸质可恢复健康。相当一部分患者对无麸质饮食无反应,被认为患有难治性乳糜泻(RCD)。目前已确认两种类型的RCD:1型RCD的特征是上皮内淋巴细胞(IEL)多克隆群体,免疫表型正常;2型RCD表现为具有异常免疫谱的单克隆IEL。RCD患者发生诸如溃疡性空肠炎(UJ)和肠病型T细胞淋巴瘤(ETTL)等并发症的风险很高。RCD2可能代表明显淋巴瘤发展的早期阶段。因此,RCD的诊断具有重要意义,但仍然是一个具有挑战性的领域。在本文中,我们回顾了RCD的最新进展,包括诊断方法以及对RCD及其并发症的关键临床、组织学、免疫组化和分子特征的讨论。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验