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自身免疫性肠病与类风湿关节炎:自身免疫领域的一种新关联。

Autoimmune enteropathy and rheumatoid arthritis: a new association in the field of autoimmunity.

作者信息

Volta U, De Angelis G L, Granito A, Petrolini N, Fiorini E, Guidi M, Muratori P, Bianchi F B

机构信息

Department of Internal Medicine, Cardioangiology, Hepatology, University of Bologna, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138 Bologna, Italy.

出版信息

Dig Liver Dis. 2006 Dec;38(12):926-9. doi: 10.1016/j.dld.2006.02.003. Epub 2006 Aug 21.

Abstract

We report the case of a 35-year-old woman with a diagnosis of coeliac disease at the age of 32 due to a severe malabsorption and flat mucosa without endomysial and tissue transglutaminase antibodies. The lack of clinical and histological improvement after 1 year of a gluten-free diet led to a diagnosis of refractory sprue. She had a good clinical response to steroids that were stopped after 3 months when she became pregnant. After delivery, she again started to complain of malabsorption with arthritis. Positivity for enterocyte autoantibodies together with a flat mucosa persistence allowed to identify a condition of autoimmune enteropathy; moreover, a rheumatological assessment gave evidence of an associated rheumatoid arthritis. Treatment by steroids and methotrexate brought to the remission of intestinal and articular symptoms together with an improvement of duodenal histology. This is the first description of an autoimmune enteropathy associated with rheumatoid arthritis. Autoimmune enteropathy should be always ruled out in patients with a villous atrophy unresponsive to a gluten-free diet, autoimmune manifestations and negativity of coeliac disease markers.

摘要

我们报告了一名35岁女性的病例,该女性在32岁时因严重吸收不良和平坦黏膜被诊断为乳糜泻,但其肌内膜和组织转谷氨酰胺酶抗体呈阴性。无麸质饮食1年后临床和组织学均无改善,导致诊断为难治性口炎性腹泻。她对类固醇治疗有良好的临床反应,在怀孕3个月后停用。分娩后,她再次开始抱怨吸收不良并伴有关节炎。肠细胞自身抗体呈阳性以及黏膜持续平坦,提示存在自身免疫性肠病;此外,风湿科评估显示伴有类风湿关节炎。类固醇和甲氨蝶呤治疗使肠道和关节症状缓解,十二指肠组织学也有所改善。这是首次描述与类风湿关节炎相关的自身免疫性肠病。对于无麸质饮食无反应的绒毛萎缩、有自身免疫表现且乳糜泻标志物阴性的患者,应始终排除自身免疫性肠病。

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