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ArticleFrontiers in immunology2026

Tuberculous meningoencephalitis concurrent with autoimmune glial fibrillary acidic protein astrocytopathy: a case report.

Yuan Deng, Zeyan Bao, SiDian Zhuang, Ting Wu, ShuiSheng Zhong

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Article in Frontiers in immunology, 2026. 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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1 · What the graph read from it

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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.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yuan DengDepartment of Neurology, Guangdong Sanjiu Brain Hospital, Guangzhou, China.
Zeyan BaoDepartment of Neurology, Guangdong Sanjiu Brain Hospital, Guangzhou, China.
SiDian ZhuangDepartment of Neurology, Guangdong Sanjiu Brain Hospital, Guangzhou, China.
Ting WuDepartment of Ultrasound Medicine, Guangdong Sanjiu Brain Hospital, Guangzhou, China.
ShuiSheng ZhongDepartment of Neurology, Guangdong Sanjiu Brain Hospital, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tuberculous meningoencephalitis and autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy display similar clinical features, cerebrospinal fluid (CSF) profiles, and neuroimaging patterns, which contribute to a high rate of misdiagnosis. Co-existence of these two diseases is extremely rare, and the clinical characteristics of this overlap syndrome remain poorly understood. Case presentation: A 67-year-old male patient was admitted with symptoms of fever, cognitive slowing, and limb weakness. Brain magnetic resonance imaging (MRI) showed multiple parenchymal signal abnormalities and leptomeningeal enhancement, associated with markedly increased intracranial pressure. The CSF showed pleocytosis, increased protein, decreased glucose, and decreased chloride levels. Simultaneously, a positive result was obtained from GeneXpert MTB/RIF, which is a diagnostic tool for tuberculous meningoencephalitis. In addition, GFAP antibodies were positive in both serum and CSF. Thus, a diagnosis of tuberculous meningoencephalitis and GFAP astrocytopathy was made. The patient showed significant clinical improvement after receiving antitubercular drugs and corticosteroids. Repeat MRI after steroid discontinuation demonstrated an increase in abnormal enhancing lesions. The lesions improved after glucocorticoid reintroduction. Conclusion: Tuberculous meningoencephalitis and GFAP astrocytopathy represent a rare overlap syndrome, and these cases are potentially susceptible to therapeutic paradoxical reactions, which are visible on imaging studies. Therapy for these cases involves concomitant anti-infective and immunomodulatory therapy, with consideration for the timing of steroid tapering and discontinuation.

Indexed as

AstrocytesAutoantibodiesGlial Fibrillary Acidic ProteinMeningoencephalitisTuberculosis, MeningealAgedAntitubercular AgentsBiomarkersHumansMagnetic Resonance ImagingMaleMycobacterium tuberculosisAntitubercular AgentsAutoantibodiesBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteincase reportglial fibrillary acidic proteinoverlap syndromeparadoxical reactiontuberculous meningoencephalitis

Identifiers

PMID42548599
PMCPMC13429656

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