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乳糜泻的诊断:批判性综述。

Diagnosing celiac disease: A critical overview.

作者信息

Ensari Arzu, Marsh Michael N

机构信息

Department of Pathology, Ankara University School of Medicine, Ankara, Turkey.

Wolfson College, University of Oxford, Oxford, UK.

出版信息

Turk J Gastroenterol. 2019 May;30(5):389-397. doi: 10.5152/tjg.2018.18635.

Abstract

The diagnosis of celiac disease (CD) no longer rests on a malabsorptive state or severe mucosal lesions. For the present, diagnosis will always require the gold-standard of a biopsy, interpreted through its progressive phases (Marsh classification). Marsh classification articulated the immunopathological spectrum of gluten-induced mucosal changes in association with the recognition of innate (Marsh I infiltration) and T cell-based adaptive (Marsh II, and the surface re-organisation typifying Marsh III lesions) responses. Through the Marsh classification the diagnostic goalposts were considerably widened thus, over its time-course, permitting countless patients to begin a gluten-free diet but who, on previous criteria, would have been denied such vital treatment. The revisions of this classification failed to provide additional insight in the interpretation of mucosal pathology. Morever, the subclassification of Marsh 3 imposed an enormous amount of extra work on pathologists with no aid in diagnosis, treatment, or prognosis. Therefore, it should now be apparent that if gastroenterologists ignore these sub-classifications in clinical decision-making, then on that basis alone, there is no need whatsoever for pathologists to persist in reporting them. Since new treatments are under critical assessment, we might have to consider use of some other higher level histological techniques sensitive enough to detect the changes sought. A promising alternative would be to hear more voices from imaginative histopathologists or morphologists together with some more insightful approaches, involving molecular-based techniques and stem cell research may be to evaluate mucosal pathology in CD.

摘要

乳糜泻(CD)的诊断不再依赖于吸收不良状态或严重的黏膜病变。目前,诊断始终需要活检这一金标准,并通过其进展阶段(马什分类法)进行解读。马什分类法阐明了麸质诱导的黏膜变化的免疫病理学谱,同时认识到先天性(马什I型浸润)和基于T细胞的适应性(马什II型,以及典型的马什III型病变的表面重组)反应。通过马什分类法,诊断标准大幅拓宽,因此,在其发展过程中,无数患者得以开始无麸质饮食,但按照以前的标准,他们会被拒绝这种至关重要的治疗。该分类法的修订未能在黏膜病理学解读方面提供更多见解。此外,马什3型的细分给病理学家带来了大量额外工作,对诊断、治疗或预后并无帮助。因此,现在应该很明显,如果胃肠病学家在临床决策中忽略这些细分,那么仅基于这一点,病理学家就完全没有必要坚持报告它们。由于新疗法正在接受严格评估,我们可能不得不考虑使用一些其他更高级的组织学技术,这些技术足够敏感,能够检测到所寻求的变化。一个有前景的替代方法可能是更多地听取富有想象力的组织病理学家或形态学家的意见,以及一些更有见地的方法,包括基于分子的技术和干细胞研究,可能用于评估乳糜泻中的黏膜病理学。

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