Pediatric choroid plexus papilloma arising from the cerebellopontine angle: systematic review with illustrative case

Mairre James S Gaddi1, Jeffrey I Lappay2, Kevin Ivan P Chan3

  • 1Division of Neurosurgery, Department of Neurosciences, University of the Philippines - Philippine General Hospital, Manila, Philippines. msgaddi1@up.edu.ph.

Insights

Pediatric choroid plexus papillomas in the cerebellopontine angle are rare. This systematic review of 11 cases shows surgical resection leads to excellent outcomes and recovery for children.

Area of Science:

  • Neuro-oncology
  • Pediatric Neurosurgery
  • Central Nervous System Tumors

Background:

  • Choroid plexus tumors are uncommon intraventricular neoplasms originating from the choroid plexus.
  • Choroid plexus papillomas in the cerebellopontine angle are exceptionally rare in children, typically affecting adults.

Purpose of the Study:

  • To systematically review pediatric choroid plexus papillomas in the cerebellopontine angle.
  • To analyze clinical presentation, imaging, management, and outcomes in this rare pediatric population.

Main Methods:

  • Systematic review of case reports and series from SCOPUS and PubMed adhering to PRISMA guidelines.
  • Inclusion of one additional case managed at the reporting center for a total of eleven cases.

Main Results:

  • Eleven pediatric cases of cerebellopontine angle choroid plexus papillomas were identified (median age 8 years, female predilection).
  • Common symptoms included headache, cerebellar signs, and cranial nerve palsies (median duration 4 months).
  • All patients underwent surgery with gross total excision achieved in most; no deaths reported at 12-month follow-up, with significant neurologic recovery.

Conclusions:

  • Pediatric choroid plexus papillomas in the cerebellopontine angle are rare but important differential diagnoses.
  • Complete surgical resection is the primary treatment modality.
  • Excellent outcomes and recovery are achievable with timely surgical intervention.
Abstract

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