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Published on: September 20, 2024
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.
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.
Abstract:
We present an interesting report of a 5-month-old infant with epileptic spasms and developmental delay who presented with non-isolated ventriculomegaly in utero and whose brain magnetic resonance imaging revealed right ventricular choroid plexus papilloma (CPP). The epileptic spasms persisted even with the use of antiepileptic therapies but was apparently cured after the removal of a CPP.
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