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利妥昔单抗成功治疗类风湿性肉芽肿病和硬脑膜炎。

Rheumatoid granulomatous disease and pachymeningitis successfully treated with rituximab.

作者信息

Moeyersoons Anneleen, Verschueren Patrick, Tousseyn Thomas, De Langhe Ellen

机构信息

a Division of Rheumatology , University Hospitals Leuven , Leuven , Belgium.

b Department of Pathology , University Hospitals Leuven , Leuven , Belgium.

出版信息

Acta Clin Belg. 2018 Aug;73(4):307-312. doi: 10.1080/17843286.2017.1375193. Epub 2017 Sep 13.

Abstract

Granulomatous disease and pachymeningitis rarely occur in rheumatoid arthritis patients and confer a challenging differential diagnosis. Our patient, treated with a tumor necrosis factor alpha inhibitor, presented with meningitis and diffuse granulomatous adenopathies. Opportunistic infections and malignancy were excluded after confirmation of negative broath serologic, molecular analysis, and negative cytology. Because of the time frame and the clinical presentation, this case was considered as a rare systemic manifestation of RA. He was treated with rituximab with beneficial clinical evolution. This case offers an excellent opportunity to focus on the diagnostic and therapeutic approach in pachymeningitis and granulomatous disease in rheumatoid arthritis patients.

摘要

肉芽肿病和硬脑膜炎在类风湿关节炎患者中很少见,诊断颇具挑战性。我们的患者接受肿瘤坏死因子α抑制剂治疗后,出现了脑膜炎和弥漫性肉芽肿性淋巴结病。在确认肉汤血清学、分子分析均为阴性且细胞学检查结果为阴性后,排除了机会性感染和恶性肿瘤。鉴于发病时间和临床表现,该病例被认为是类风湿关节炎罕见的全身表现。他接受了利妥昔单抗治疗,临床病情有所改善。该病例为关注类风湿关节炎患者硬脑膜炎和肉芽肿病的诊断及治疗方法提供了绝佳机会。

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