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模仿结核性脑膜炎的MOG阳性原发性自身免疫性脑膜炎:病例系列

MOG positive primary autoimmune meningitis mimicking tuberculous meningitis: a case series.

作者信息

Shivarthi Tejas, Sriram Mahima, Nikhilesh Muddana, Kannoth Sudheeran, Nambiar Vivek, Gopinath Siby, Umesh Saraf Udit, Unnikrishnan Gopikrishnan, Kumar Anand, Mathai Annamma, Thevarkalam Meena

机构信息

Department of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.

Neuroimmunology Laboratory, Department of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India.

出版信息

BMJ Neurol Open. 2025 Apr 27;7(1):e000999. doi: 10.1136/bmjno-2024-000999. eCollection 2025.

Abstract

OBJECTIVES

Primary autoimmune meningitis presentation of myelin oligodendrocyte glycoprotein (MOG) IgG antibody positivity is infrequently reported. We aim to identify the patients with MOG IgG antibody positivity who were initially misdiagnosed and treated as tuberculous meningitis (TBM).

METHODS

A retrospective cross-sectional study conducted in the Neuroimmunology Laboratory and Department of Neurology of Amrita Institute of Medical Sciences, Kochi, Kerala, India between June 2018 and December 2023. MOG IgG antibody positive cases were identified from the Neuroimmunology Lab Registry, and the case sheets were screened for TBM-like presentation. Cases were included on the basis of MOG IgG positivity, an initial diagnosis of tuberculosis was suspected and antitubercular therapy was initiated with minimal response.

RESULTS

We described the clinical, microbiological, radiological and serological features of five patients with a TBM-like presentation eventually diagnosed with MOG-associated meningitis. Symptoms included headache, vomiting, visual impairment and weakness. Three patients showed normal MRIs and two patients showed MRI findings consistent with demyelination. Serum MOG antibody testing was positive only on serial testing of all five patients. The final diagnosis was MOG-associated meningitis in two patients and MOG-associated meningoencephalitis in three patients.

DISCUSSION

This case series highlights the rare presentation of MOG antibody positive patients presenting as primary autoimmune meningitis and its diagnostic challenges, especially in regions where tuberculosis is common. The study underscores the importance of considering autoimmune aetiology as a differential diagnosis when tuberculosis treatment fails or relapses occur, advocating for MOG IgG antibody testing to ensure accurate diagnosis and effective treatment.

摘要

目的

髓鞘少突胶质细胞糖蛋白(MOG)IgG抗体阳性的原发性自身免疫性脑膜炎的病例报道较少。我们旨在识别那些最初被误诊为结核性脑膜炎(TBM)并接受相应治疗的MOG IgG抗体阳性患者。

方法

2018年6月至2023年12月在印度喀拉拉邦高知市阿姆里塔医学科学研究所神经免疫学实验室和神经内科进行了一项回顾性横断面研究。从神经免疫学实验室登记处识别出MOG IgG抗体阳性病例,并筛查病例表中是否有类似TBM的表现。纳入标准为MOG IgG阳性、最初怀疑为结核病诊断且抗结核治疗反应甚微。

结果

我们描述了5例最初表现类似TBM最终诊断为MOG相关脑膜炎患者的临床、微生物学、影像学和血清学特征。症状包括头痛、呕吐、视力障碍和虚弱。3例患者MRI正常,2例患者MRI表现符合脱髓鞘改变。所有5例患者均经多次检测血清MOG抗体才呈阳性。最终诊断为2例MOG相关脑膜炎和3例MOG相关脑膜脑炎。

讨论

该病例系列突出了MOG抗体阳性患者表现为原发性自身免疫性脑膜炎的罕见情况及其诊断挑战,尤其是在结核病常见的地区。该研究强调了在结核病治疗失败或复发时将自身免疫病因作为鉴别诊断的重要性,提倡进行MOG IgG抗体检测以确保准确诊断和有效治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae6/12035451/eaeca9ab5aaa/bmjno-7-1-g001.jpg

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