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Intraventricular cryptococcal cysts masquerading as racemose neurocysticercosis
Marlon Mathews1, Laura Paré, Anton Hasso
1Department of Neurosurgery, University of California, Irvine, Orange, CA 92868.
Background:
Cryptococcal infections of the CNS are infrequent in immunocompetent hosts. When present, they usually present as meningitis and hydrocephalus or as fungal masses called cryptococcomas. We report a case in which intraventricular cryptococcal cysts clinically and radiologically simulated the racemose form of neurocysticercosis.
Case Description:
A 23-year-old man presented to the emergency department with a 1-week history of severe headache, dizziness, nausea, vomiting, and some lethargy. A computed tomography scan revealed significant hydrocephalus. The patient was admitted to the hospital and immediately underwent a right ventriculostomy tube placement. CSF examination showed a meningitic pattern. Magnetic resonance imaging, including FLAIR images, showed multiple large cysts in the temporal horns of both lateral ventricles in addition to hydrocephalus. When an endoscopic left temporal cyst fenestration failed to decompress his trapped right temporal horn, he underwent placement of a left lateral ventricle to peritoneal shunt and a right temporal cyst to peritoneal shunt. ELISA test results for HIV-1 and -2 antibodies in the patient's serum were negative. His CD4 and CD8 counts were within normal limits. Multiple tests for CSF anticysticercal antibody using IgG ELISA gave unequivocally negative results. Latex agglutination tests detected Cryptococcus neoformans antigen in his CSF in titers of 1:1024, which progressively decreased in response to antifungal therapy. The patient underwent treatment with IV amphotericin B for 7 weeks, IV 5-FC for 2 weeks, and oral fluconazole for 5 weeks. At discharge, 3 consecutive CSF cultures were negative for bacteria and fungi. His neurologic status returned to baseline.
Conclusions:
Cryptococcal CNS infections in immunocompetent hosts can mimic the intraventricular form of racemose neurocysticercosis. Distinguishing between the two is essential because the medical management of the 2 conditions is distinct from each other.
Insights
Central nervous system cryptococcal infections in immunocompetent individuals can mimic neurocysticercosis. Early diagnosis is crucial for appropriate treatment of these rare fungal CNS cysts.
Area of Science:
- Neurology
- Infectious Diseases
- Radiology
Background:
- Central nervous system (CNS) cryptococcal infections are rare in immunocompetent hosts.
- Typically present as meningitis, hydrocephalus, or cryptococcomas.
- This case highlights intraventricular cryptococcal cysts mimicking neurocysticercosis.
Observation:
- A 23-year-old male presented with severe headache, dizziness, and lethargy.
- Imaging revealed hydrocephalus and multiple intraventricular cysts.
- Cerebrospinal fluid (CSF) analysis showed a meningitic pattern, and Cryptococcus neoformans antigen was detected.
Findings:
- Despite negative neurocysticercosis serology, the presentation mimicked racemose neurocysticercosis.
- The patient received antifungal therapy including amphotericin B, 5-FC, and fluconazole.
- Neurological status returned to baseline with resolution of CSF Cryptococcus antigen.
Implications:
- CNS cryptococcal infections can present atypically in immunocompetent individuals.
- Distinguishing cryptococcal cysts from neurocysticercosis is critical due to different management strategies.
- This case underscores the importance of considering fungal infections in CNS pathologies that mimic parasitic infections.
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