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[Meningomyeloradiculitis in an immunocompetent patient]
C Carra Dalliere1, E Thouvenot, G Baptista
1Service de neurologie, hôpital Gui-de-Chauliac, CHU de Montpellier, 80 avenue Augustin-Flîche, Montpellier cedex 5, France. clarisse.dalliere@wanadoo.fr
Introduction:
Candida infection limited to the central nervous system is extremely rare, and may be confused with tuberculosis on the grounds of the clinical and cerebrospinal fluid findings.
Case Report:
A 23-year-old immunocompetent drug addict presented with alternating sciatica over a period of several months, followed by multiple cranial nerve involvement in the setting of marked weight loss. The histopathologic examination of a leptomeningeal neurosurgical biopsy was required to establish the diagnosis of neuromeningeal infection with Candida albicans.
Conclusion:
This case report underlines diagnostic difficulties of candidal meningitis and reviews current therapeutic recommendations.
Insights
Central nervous system Candida infection is rare and mimics tuberculosis. Diagnosis requires neurosurgical biopsy, highlighting challenges in candidal meningitis management.
Area of Science:
- Neurology
- Infectious Diseases
- Mycology
Background:
- Candida infection of the central nervous system (CNS) is exceptionally rare.
- Clinical and cerebrospinal fluid findings can mimic tuberculosis, complicating diagnosis.
Observation:
- A 23-year-old immunocompetent individual with a history of drug addiction presented with symptoms of alternating sciatica and multiple cranial nerve involvement.
- Significant weight loss was noted preceding the neurological deficits.
Findings:
- Diagnosis was established via histopathologic examination of a leptomeningeal neurosurgical biopsy.
- The causative agent was identified as Candida albicans, confirming neuromeningeal candidiasis.
Implications:
- This case underscores the diagnostic challenges associated with candidal meningitis.
- Current therapeutic strategies for this rare CNS fungal infection are reviewed.
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