ArticleBMJ neurology open2025
MOG positive primary autoimmune meningitis mimicking tuberculous meningitis: a case series.
Article in BMJ neurology open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Autoimmune-associated epilepsy or acute symptomatic seizures? A case series of recurrent seizures in patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD).Epilepsy research · 2026Article
- Medulloblastoma masquerading as tuberculous meningitis in a pediatric patient.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026Article
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11 authors.
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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.
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