What if neurosarcoidosis was actually tuberculosis?
English version of a poster presented in French.
Djodjo Mbiyuku1✉, K. Weyo1, G. Bennani1, F. Harim1, K. Chbani2, F. Ailal3, I. Chahib3
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Received 9 October 2026 · Accepted 9 October 2026 · Published 9 October 2026
DOI: https://doi.org/10.5281/zenodo.23349270
Article PDF · Original poster (PDF)
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Abstract
Introduction
Tuberculous meningitis remains a frequent cause of chronic meningitis in endemic countries. Some non-infectious granulomatous diseases, such as neurosarcoidosis, can closely mimic the clinical and radiological presentation, complicating differential diagnosis.
Materials and methods
Case report of a 13-year-old boy admitted for febrile intracranial hypertension syndrome with seizures. CSF analysis showed high protein, high glucose, and absence of Mycobacterium tuberculosis. Initial brain MRI suggested tuberculous meningitis. After no improvement with anti-tuberculous treatment, brain and spinal MRI showed diffuse leptomeningeal involvement. Neurosarcoidosis diagnosis was made after exclusion and treatment with corticosteroids and immunosuppressants.
Results
The patient showed notable clinical improvement after immunosuppressive treatment. Imaging revealed meningeal nodular lesions suggesting a non-infectious granulomatous cause. Etiological workup showed persistent high protein in CSF without Mycobacterium tuberculosis. Chest CT was normal.
Conclusion
This case illustrates the diagnostic challenge between tuberculous meningitis and neurosarcoidosis, especially in tuberculosis endemic areas, and highlights the importance of pathological examination to confirm the granulomatous nature of the infiltrate.
Original poster
References
- Pawar S et al. Clinical profile of tuberculous meningitis. Neurol India. 2017.
- Bathla G et al. Differentiating CNS sarcoidosis from TB. Acta Radiologica. 2018
- Boudjarane MA et al. Diagnostic pitfalls of neurosarcoidosis in TB-endemic regions. Pan Afr Med J. 2021
- Sharma SK, Mohan A. TB in high-burden countries. Indian J Med Res. 2019
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