Evidence map›Paper›PMID 40610928›Full record

ArticleBMC neurology2025

Myelin oligodendrocyte glycoprotein antibody-associated disease presenting as aseptic meningitis and multiple cranial neuritis: a case report.

Yi-Na Zhang, Qiong Wu, Yu-Hang Dong, Ying-Jie Dai

Abstract readCase Reports
In one paragraph

Article in BMC neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

4 authors.

Yi-Na Zhang *Department of Neurology, General Hospital of Northern Theater Command, 83 Wen Hua Road, Shenyang, 110016, China.
Qiong Wu *Department of Neurology, General Hospital of Northern Theater Command, 83 Wen Hua Road, Shenyang, 110016, China.
Yu-Hang DongDepartment of Neurology, General Hospital of Northern Theater Command, 83 Wen Hua Road, Shenyang, 110016, China.
Ying-Jie DaiDepartment of Neurology, General Hospital of Northern Theater Command, 83 Wen Hua Road, Shenyang, 110016, China. 15009888333@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Both aseptic meningitis and cranial neuritis are the atypical clinical manifestations of myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD), with sporadic cases of MOGAD presenting with either condition previously reported. However, no case has been documented with both of aseptic meningitis and cranial neuritis occurring concurrently. Here, we report the first such case: a 59-year-old male uniquely presenting with aseptic meningitis and multiple cranial neuritis simultaneously. Diagnosis of MOGAD was confirmed by positive MOG antibody titers in both serum and cerebrospinal fluid. Following corticosteroid treatment, the clinical symptoms, cerebrospinal fluid parameters, and imaging findings related to aseptic meningitis improved. Paradoxically, the cranial neuritis symptoms worsened. Regrettably, the patient succumbed to extreme debilitation and dysphagia ten days post-discharge. This case underscores the importance of considering MOGAD in patients presenting with concurrent aseptic meningitis and multiple cranial neuritis. Notably, compromised physical status may be a critical determinant of poor prognosis in such cases.

Indexed as

Cranial Nerve DiseasesMeningitis, AsepticMyelin-Oligodendrocyte GlycoproteinMyelin Oligodendrocyte Glycoprotein Antibody-Associated DiseaseAutoantibodiesHumansMaleMiddle AgedAutoantibodiesMyelin-Oligodendrocyte GlycoproteinAseptic meningitisCranial neuritisMyelin oligodendrocyte glycoprotein antibody associated disease

Identifiers

PMID40610928
PMCPMC12231948

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