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Author Spotlight: Studying Behavior of Acanthamoeba to Develop Targeted Strategies for Preventing Acanthamoeba Keratitis
Published on: September 20, 2024
Non-granulomatous cerebellar infection by Acanthamoeba spp. in an immunocompetent host
Sara Modica1,2, Clelia Miracco3, Maria Grazia Cusi4,2
1Hospital Department of Specialized and Internal Medicine, Infectious Diseases Unit, University Hospital of Siena, Siena, Italy.
Abstract:
Acanthamoeba spp. is a free-living amoeba, frequently involved in keratitis by contact lens in immunocompetent hosts. Anecdotal reports associate Acanthamoeba spp. as a cause of severe granulomatous encephalitis in immunocompromised and, less frequently, in immunocompetent subjects. Data regarding clinical and therapeutic management are scanty and no defined therapeutic guidelines are available. We describe an unusual case of non-granulomatous Acanthamoeba cerebellitis in an immunocompetent adult male, with abrupt onset of neurological impairment, subtle hemorrhagic infarction at magnetic resonance imaging, and initial suspicion of cerebellar neoplasm. Histopathological findings of excised cerebellar mass revealed the presence of necrosis and inflammation with structure resembling amoebic trophozoites, but without granulomas. Polymerase chain reaction from cerebellar tissue was positive for Acanthamoeba T4 genotype. Due to gastrointestinal intolerance to miltefosine, the patient was treated with long-term course of fluconazole and trimethoprim/sulphamethoxazole, obtaining complete clinical and neuroradiological resolution.
Insights
Acanthamoeba cerebellitis, a rare brain infection, occurred in an immunocompetent patient. Treatment with fluconazole and trimethoprim/sulfamethoxazole led to full recovery.
Area of Science:
- Neurology
- Infectious Diseases
- Ophthalmology
Background:
- Acanthamoeba spp. commonly cause keratitis in contact lens wearers.
- Acanthamoeba infections of the central nervous system are rare, particularly non-granulomatous forms in immunocompetent individuals.
- Limited clinical data and treatment guidelines exist for Acanthamoeba CNS infections.
Observation:
- An immunocompetent adult male presented with sudden neurological decline.
- Magnetic resonance imaging revealed cerebellar infarction, initially suspected as a neoplasm.
- Histopathology of the cerebellar mass showed necrosis and inflammation with amoebic forms but no granulomas.
Findings:
- Polymerase chain reaction confirmed Acanthamoeba T4 genotype in cerebellar tissue.
- The patient experienced gastrointestinal intolerance to miltefosine.
- A combination therapy of fluconazole and trimethoprim/sulfamethoxazole was administered.
Implications:
- This case highlights a rare presentation of Acanthamoeba cerebellitis in an immunocompetent host.
- Successful treatment with fluconazole and trimethoprim/sulfamethoxazole offers an alternative therapeutic option.
- Further research is needed to establish definitive treatment guidelines for CNS Acanthamoeba infections.
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