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Choroid plexus tumor in a child.

M A St John¹, H Clarke

¹Department of Pediatrics, Queen Elizabeth Hospital, Barbados, West Indies.

Journal of the National Medical Association

|October 1, 1992

Summary

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A rare choroid plexus papilloma was diagnosed in a 5-month-old infant presenting with concerning neurological symptoms. Early detection is crucial for managing this pediatric brain tumor.

Area of Science:

Pediatric Neurology
Neuro-oncology
Developmental Pediatrics

Background:

Choroid plexus papillomas are rare tumors typically affecting children.
Hydrocephalus is a common complication due to cerebrospinal fluid obstruction.

Observation:

A 5-month-old infant presented with fever and nonspecific symptoms.
Rapidly increasing head circumference and regression in motor development were noted.

Findings:

Diagnostic investigations confirmed a choroid plexus papilloma.
This diagnosis explains the infant's progressive neurological decline.

Implications:

Highlights the importance of considering rare pediatric brain tumors in infants with developmental regression.

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Emphasizes the need for prompt neuroimaging and intervention for hydrocephalus.

Underscores the significance of early diagnosis for improved patient outcomes in pediatric neuro-oncology.