Evidence map›Paper›PMID 40297746›Full record

ArticleBMJ neurology open2025

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

Tejas Shivarthi, Mahima Sriram, Muddana Nikhilesh, Sudheeran Kannoth, Vivek Nambiar, Siby Gopinath, Saraf Udit Umesh, Gopikrishnan Unnikrishnan, Anand Kumar, Annamma Mathai and 1 more

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Medulloblastoma masquerading as tuberculous meningitis in a pediatric patient.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Tejas ShivarthiDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.ORCID 0009-0002-5814-902X
Mahima SriramDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Muddana NikhileshDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Sudheeran KannothDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.ORCID 0000-0001-7049-2774
Vivek NambiarDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Siby GopinathDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Saraf Udit UmeshDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Gopikrishnan UnnikrishnanDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Anand KumarDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Annamma MathaiDepartment of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India.
Meena ThevarkalamNeuroimmunology Laboratory, Department of Neurology, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

NEUROIMMUNOLOGYTUBERCULOSIS

Identifiers

PMID40297746
PMCPMC12035451

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