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Fungal meningoencephalitis caused by Alternaria: a clinical case
Cícero J C Silveira1, Joana Amaral, Rodrigo P Gorayeb
1Neurosurgery Service, Hospital Egas Moniz - Centro Hospitalar de Lisboa Ocidental, EPE, Lisbon, Portugal. cjeancs@yahoo.com.br
Abstract:
Cerebral phaeohyphomycosis is an infrequent infectious condition associated with a high mortality rate. The authors describe a very rare case that occurred in an immunocompetent 18-year-old man who developed severe meningoencephalitis and arachnoiditis caused by Alternaria alternata, which were diagnosed in the context of difficult-to-treat hydrocephalus. Etiological diagnosis was made based on fungal culture and histopathologic examination. Empirical treatment consisted of an early aggressive antifungal combination therapy consisting of intravenous liposomal amphotericin B (5 mg/kg per day) and voriconazole (4 mg/kg every 12 h), which initially induced a favorable response. Following the fungus identification, the choice for the combination of posaconazole (400 mg every 12 h) plus flucytosine (4000 mg/day) proved to be effective in the suppression of the signs and symptoms of this uncommon cerebral mycosis. At a 12-month follow-up visit no recurrence had occurred and posaconazole was then stopped.
Insights
This study reports a rare case of cerebral phaeohyphomycosis in an immunocompetent young man caused by Alternaria alternata. Effective treatment involved combination antifungal therapy, leading to symptom suppression and no recurrence.
Area of Science:
- Neurology
- Infectious Diseases
- Mycology
Background:
- Cerebral phaeohyphomycosis is a rare and often fatal fungal infection of the brain.
- It typically affects immunocompromised individuals, making this case in an immunocompetent host highly unusual.
Observation:
- An 18-year-old immunocompetent male presented with severe meningoencephalitis and arachnoiditis.
- The condition was linked to difficult-to-treat hydrocephalus and diagnosed via fungal culture and histopathology.
- The causative agent was identified as Alternaria alternata.
Findings:
- Initial empirical treatment with liposomal amphotericin B and voriconazole showed a positive response.
- Subsequent targeted therapy with posaconazole and flucytosine effectively suppressed the fungal infection's signs and symptoms.
- A 12-month follow-up confirmed no recurrence of the cerebral mycosis.
Implications:
- This case highlights the importance of considering rare fungal infections like cerebral phaeohyphomycosis even in immunocompetent patients.
- Successful management underscores the efficacy of aggressive combination antifungal therapy tailored to specific fungal pathogens.
- The findings contribute to understanding treatment strategies for uncommon central nervous system mycoses.
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