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Cryptococcal Meningitis in an Immunocompetent Patient With an Initially False-Negative Cerebrospinal Fluid Analysis:
Sheau Wei Tan1, Chuin Chi Yap1, Sri Siva Shakti Ratanasamy1
1Internal Medicine, Hospital Sultanah Nora Ismail, Batu Pahat, MYS.
Insights
Cryptococcal meningitis (CM) can occur in immunocompetent individuals, presenting diagnostic challenges. Early suspicion and serial testing are crucial for timely cryptococcus neoformans diagnosis and treatment.
Area of Science:
- Neurology
- Infectious Diseases
- Medical Diagnostics
Background:
- Cryptococcal meningitis (CM) is typically linked to immunocompromised states.
- Its occurrence in immunocompetent individuals is rising and presents diagnostic difficulties.
- Subacute meningoencephalitis and hydrocephalus can be initial symptoms.
Abstract:
Cryptococcal meningitis (CM) is traditionally associated with immunocompromised states, such as HIV/AIDS. However, its presentation in immunocompetent hosts is increasingly recognized and frequently poses a diagnostic dilemma. A 56-year-old immunocompetent male presented with obstructive hydrocephalus following a month of worsening headaches. Initial cerebrospinal fluid (CSF) analysis, including India ink, cryptococcal antigen, and cultures obtained during ventriculoperitoneal shunt placement, was unremarkable. Subsequent brain MRI demonstrated evolving leptomeningeal enhancement and small cerebellar nodules. Due to clinical overlap, the patient was empirically treated for tuberculosis but developed an adverse cutaneous reaction. Driven by worsening imaging findings, repeat CSF studies were performed; fungal culture and PCR eventually confirmed Cryptococcus neoformans. The patient was treated with induction amphotericin B and flucytosine, followed by maintenance fluconazole, resulting in a full clinical and radiological recovery. This case emphasizes that CM must remain a differential diagnosis in subacute meningoencephalitis or unexplained hydrocephalus, regardless of immune status. High clinical suspicion warrants serial CSF sampling and molecular diagnostics to prevent delayed treatment of this potentially fatal infection.
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