重叠综合征患者的类风湿脑膜炎:脑脊液中抗瓜氨酸肽抗体测定的有效性。

Pablo Lorenzo Barreto, Garbiñe Roy Ariño, Fernando Pérez Trapote, Alberto Sáez Marín, Erik S Stiauren Fernández, Beatriz Zarza Sanz, Nuria García Barragán, Carlos de la Puente Bujidos, F Javier Buisán Catevilla
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摘要

类风湿脑膜炎(RM)是一种罕见的并发症,可表现为中风样发作的类风湿关节炎。我们提出的情况下,63岁的妇女重叠综合征的历史和临床表现提示的amyopathic皮肌炎,类风湿性关节炎和系统性红斑狼疮。她以突然出现的右侧笨拙和麻木以及2周的左半颅头痛病史就诊于急诊科。实验室检查显示血清抗核抗体、抗ro抗体、抗瓜氨酸肽抗体(ACPA)阳性,类风湿因子升高。淋巴细胞增多,ACPA和抗ro抗体阳性,呈被动扩散模式,微生物学研究阴性。脑磁共振成像以左侧额顶枕轻脑膜和厚脑膜增强为主。她被诊断为RM,并接受甲基强的松龙IV mg/kg每日1次。脑脊液(CSF)淋巴细胞增多症和脑膜增强患者出现脑卒中样发作时,应提高对RM的怀疑。在这种情况下,应始终测量血清类风湿因子和ACPA水平,同时也应测量CSF中的ACPA。据我们所知,这是首次报道的重叠综合征背景下的RM病例。CSF中ACPA水平可能是中枢神经系统紊乱和重叠自身免疫性疾病(包括类风湿关节炎)的相关诊断线索。在我们的病例中,当ACPA存在于中枢神经系统时,即使没有鞘内合成的证据,提示RM的临床情况也加强了ACPA可能的致病作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rheumatoid meningitis in a patient with overlap syndrome: The usefulness of anti-citrullinated peptide antibodies determination in CSF.

Rheumatoid meningitis (RM) is a rare complication of rheumatoid arthritis that can manifest as stroke-like episodes. We present the case of a 63-year-old woman with a past history of overlap syndrome and clinical manifestations suggestive of amyopathic dermatomyositis, rheumatoid arthritis, and systemic lupus erythematosus. She presented to the emergency department with sudden onset right-sided clumsiness and numbness, as well as a 2-week history of left hemicranial headache. Laboratory workup revealed positive serum antinuclear antibodies, anti-Ro antibodies, anti-citrullinated peptide antibodies (ACPA), and elevated rheumatoid factor. Lymphocytic pleocytosis, positive ACPA and anti-Ro antibodies with passive diffusion pattern, and negative microbiological studies were demonstrated in the CSF. Brain magnetic resonance imaging showed predominant left fronto-parieto-occipital leptomeningeal and pachimeningeal enhancement. She was diagnosed with RM and received methylprednisolone IV mg/kg once daily. Stroke-like episodes in the setting of a patient with lymphocytic pleocytosis in the cerebrospinal fluid (CSF) and meningeal enhancement should raise suspicion of RM. In this context, serum rheumatoid factor and ACPA levels should always be measured and ACPA should also be measured in CSF. To our knowledge, this is the first reported case of RM in the context of an overlap syndrome. ACPA levels in CSF could be a relevant diagnostic clue in the setting of central nervous system disturbance and overlapping autoimmune conditions that include rheumatoid arthritis. In our case, the presence of a suggestive clinical scenario of RM reinforces the probable pathogenic role of ACPA when it is present in the central nervous system, even without intrathecal synthesis evidence.

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