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[Choroid plexus papilloma (author's transl)]

J Motte, P Rousseaux, J Couchot

Archives Francaises De Pediatrie

|November 1, 1981

Summary

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A choroid plexus papilloma case highlights unique hydrocephalus features. Despite tumor benignity, prognosis is often poor, though this specific case showed no growth over five years.

Area of Science:

Neuro-oncology
Neurosurgery
Pediatric Neurology

Background:

Choroid plexus papillomas are rare tumors arising from the choroid plexus epithelium.
These tumors can cause obstructive hydrocephalus due to excessive cerebrospinal fluid production.
While histologically benign, they can exhibit aggressive behavior and poor outcomes.

Observation:

A novel case of choroid plexus papilloma is presented.
The associated hydrocephalus demonstrated distinct clinical and radiological characteristics.
Computed Axial Tomography (CAT) scans were utilized for diagnosis.

Findings:

The reported tumor exhibited a lack of size increase over a five-year surveillance period, as evidenced by serial radiological imaging.
Despite the benign nature of the tumor and surgical intervention, the overall prognosis remains guarded.

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Implications:

This case underscores the variable clinical behavior of choroid plexus papillomas.
It highlights the importance of long-term radiological monitoring even in histologically benign tumors.
Understanding the specific features of hydrocephalus associated with these tumors is crucial for surgical planning and patient management.