Suppr超能文献

难治性乳糜泻

Refractory celiac disease.

作者信息

Rishi Abdul R, Rubio-Tapia Alberto, Murray Joseph A

机构信息

a Division of Gastroenterology and Hepatology , Mayo Clinic , Rochester , MN , USA.

出版信息

Expert Rev Gastroenterol Hepatol. 2016;10(4):537-46. doi: 10.1586/17474124.2016.1124759. Epub 2015 Dec 16.

Abstract

Refractory celiac disease (RCD) affects patients who have failed to heal after 6-12 months of a strict gluten-free diet (GFD) and when other causes of symptoms (including malignancy) have been ruled out. It may also occur in patients who previously had responded to a long-term GFD. RCD may be categorized as RCD1 (normal immunophenotype) and RCD2 (aberrant immunophenotype). RCD1 usually responds to a continued GFD, nutritional support, and therapeutic agents such as corticosteroids. In contrast, clinical response in RCD2 is incomplete and prognosis is often poor. RCD (particularly RCD2) is associated with serious complications, such as ulcerative jejunitis and enteropathy-associated T-cell lymphoma (EATL). Strict clinical and laboratory criteria should be used to diagnose RCD and specialized tests for aberrancy and clonality should be interpreted in the context of their sensitivity and specificity. Adequate nutritional support and anti-inflammatory treatment may even allow patients with RCD2 to attain a clinical remission.

摘要

难治性乳糜泻(RCD)影响那些在严格遵循无麸质饮食(GFD)6至12个月后仍未痊愈且已排除其他症状原因(包括恶性肿瘤)的患者。它也可能发生在先前对长期GFD有反应的患者身上。RCD可分为RCD1(正常免疫表型)和RCD2(异常免疫表型)。RCD1通常对持续的GFD、营养支持以及皮质类固醇等治疗药物有反应。相比之下,RCD2的临床反应不完全,预后通常较差。RCD(尤其是RCD2)与严重并发症相关,如溃疡性空肠炎和肠病相关T细胞淋巴瘤(EATL)。应使用严格的临床和实验室标准来诊断RCD,并且应根据其敏感性和特异性来解读针对异常和克隆性的专门检测结果。充足的营养支持和抗炎治疗甚至可能使RCD2患者实现临床缓解。

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