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Cryptococcal meningitis causing obstructive hydrocephalus in a patient on fingolimod
Chengde Pham1, Iwan Bennett1, Rondhir Jithoo1
1Department of Neurosurgery, Alfred Health, Melbourne, Victoria, Australia.
Abstract:
Cryptococcosis is a recognised opportunistic infection in immunocompromised patients. The long-term adverse effect profile of fingolimod, an immunomodulating agent approved for use in multiple sclerosis in 2010, is only just emerging. We report the first case to our knowledge of a patient presenting with obstructive hydrocephalus secondary to cryptococcal meningitis in the setting of fingolimod therapy. Extensive posterior fossa leptomeningeal inflammation with associated cerebellar oedema resulted in effacement of the fourth ventricle and obstructive hydrocephalus requiring urgent ventriculostomy. Induction, consolidative and maintenance antifungal therapy was prescribed and subsequent conversion to a ventriculoperitoneal shunt was successful in relieving the patient's ventriculomegaly. Awareness of these rare, novel and life-threatening complications of fingolimod-associated immunocompromise is critical as the use of such drugs is expected to rise.
Insights
Fingolimod therapy for multiple sclerosis can lead to rare, life-threatening cryptococcal meningitis causing obstructive hydrocephalus. Early recognition and antifungal treatment are critical for managing this adverse effect.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Fingolimod is an immunomodulating drug used for multiple sclerosis.
- Opportunistic infections like cryptococcosis are risks in immunocompromised individuals.
Observation:
- A case of cryptococcal meningitis with obstructive hydrocephalus in a patient on fingolimod therapy is presented.
- The meningitis caused posterior fossa leptomeningeal inflammation and cerebellar edema, leading to fourth ventricle effacement.
Findings:
- The patient required urgent ventriculostomy for obstructive hydrocephalus.
- Antifungal therapy and subsequent ventriculoperitoneal shunt placement successfully managed the hydrocephalus and ventriculomegaly.
Implications:
- This case highlights a rare but severe complication of fingolimod-induced immunosuppression.
- Increased awareness is crucial for clinicians as fingolimod use expands.
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