Trichosporon Asahii Meningitis in an Adult with Myelin Oligodendrocyte Glycoprotein-associated Myelitis: A Case Report and Review of Literature from North Western India
Sidhya chaudhary1, Divanshu Sharma2
1Dr. Sampurnanand Medical College, Jodhpur, 2Government medical college, Patiala
Objective:
To describe the first known case of Trichosporon Asahii meningitis in a patient with MOG antibody–associated myelitis and review relevant literature.
Background:
Trichosporon asahii is an emerging opportunistic yeast that causes invasive infections with high mortality, particularly in immunocompromised hosts. Central nervous system (CNS) dissemination is exceedingly rare, and its occurrence in patients with myelin oligodendrocyte glycoprotein-associated disease (MOGAD) has not been reported previously.
Design/Methods:
Clinical, radiological, and microbiological data were collected and analyzed. Identification of the fungal isolate was performed using VITEK MS MALDI-TOF (matrix-assisted laser desorption/ionization time-of-flight mass spectrometry).
Results:
A 44-year-old immunocompetent male presented with sudden onset fever, paraparesis, and bladder incontinence. MRI revealed T2/FLAIR hyperintensities at D12–L1, and serum MOG antibodies were positive, confirming MOG-associated myelitis. He improved with corticosteroids and azathioprine but re-presented 44 days later with headache and vomiting. CSF showed elevated protein, and fungal culture yielded T. asahii. The patient received intravenous followed by oral fluconazole, achieving complete recovery.
Conclusions:
This case expands the spectrum of CNS fungal infections associated with immune-mediated demyelinating disorders. It underscores the importance of considering opportunistic fungi in patients receiving immunosuppressive agents, even when otherwise immunocompetent. Rapid identification through MALDI-TOF and prompt antifungal therapy are critical for favorable outcomes.
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