Infantile epileptic spasms syndrome as an initial presentation in infantile choroid plexus papilloma: A case report

Faliang Zhou1, Yu Li2, Lixue Shen2

  • 1Department of Pediatrics, Peking University First Hospital, Beijing, China.

Frontiers in Pediatrics
|December 5, 2022
PubMed

Insights

A choroid plexus papilloma (CPP) in a 5-month-old infant caused epileptic spasms and developmental delay. Surgical removal of the CPP successfully resolved the infant's seizures.

Area of Science:

  • Neuroscience
  • Pediatric Neurology
  • Developmental Pediatrics

Background:

  • Epileptic spasms in infants can be challenging to manage, often requiring extensive diagnostic workups.
  • Developmental delay is a significant concern in pediatric neurology, necessitating identification of underlying causes.
  • Ventriculomegaly, an enlargement of the brain's ventricles, can be detected prenatally and warrants further investigation.

Observation:

  • A 5-month-old infant presented with a history of epileptic spasms and developmental delay.
  • Prenatal imaging revealed non-isolated ventriculomegaly.
  • Brain magnetic resonance imaging (MRI) identified a right ventricular choroid plexus papilloma (CPP).

Findings:

  • The infant's epileptic spasms were refractory to multiple antiepileptic drug therapies.
  • Following surgical removal of the choroid plexus papilloma, the infant's epileptic spasms resolved completely.
  • This suggests a direct causal link between the CPP and the infantile spasms.

Implications:

  • Choroid plexus papillomas should be considered in the differential diagnosis of infantile spasms, especially when associated with ventriculomegaly.
  • Early diagnosis and surgical intervention for CPP may lead to favorable neurological outcomes in affected infants.
  • This case highlights the importance of comprehensive neuroimaging in infants with refractory epilepsy and developmental concerns.