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Endoscopic Third Ventriculostomy and Pineal Biopsy from a Single Entry Point
Published on: June 28, 2024
Papillary pineocytoma in child: a case report.
Wiesław Marcol1, Katarzyna Kotulska, Wiesława Grajkowska
1Department of Physiology, Medical University of Silesia, Katowice, Poland. Vie@alpha.net.pl
Summary
A rare papillary pineocytoma in a child was successfully treated with surgical resection and adjuvant therapy, showing no recurrence after six years. This case highlights effective management for aggressive pineal gland tumors.
Area of Science:
- Pediatric neurosurgery
- Neuro-oncology
- Rare tumors
Background:
- Papillary pineocytoma is an exceptionally rare brain tumor.
- These tumors are typically associated with poor patient outcomes.
Observation:
- A 10-year-old girl presented with a pineal gland tumor causing obstructive hydrocephalus.
- Magnetic Resonance Imaging (MRI) was used for diagnosis.
Findings:
- The patient underwent successful ventriculoperitoneal shunt insertion and tumor resection via a supracerebellar-infratentorial approach.
- Histopathology confirmed a papillary pineocytoma.
- The tumor was treated with radio- and chemotherapy due to its aggressive nature.
Implications:
- The patient remains symptom-free with no tumor recurrence at a six-year follow-up.
- This case demonstrates a favorable outcome following aggressive management of a rare pediatric pineal tumor.