Related Experiment Videos
Multiple meningiomas in a child
T Tomita1, M A Radkowski, F Gonzalez-Crussi
1Department of Radiology, Children's Memorial Hospital, Chicago, Illinois 60614.
Abstract:
We report the case of a 4-year, 5-month-old boy, who had unusual multiple meningiomas occurring simultaneously in the intracranial, intraorbital, and spinal spaces. All lesions were surgically excised and histologically proved. This is the youngest patient with multiple meningiomas without history of neurofibromatosis reported in the literature.
Insights
This study details a rare case of multiple meningiomas in a young child affecting the brain, eye socket, and spine. The patient, the youngest reported without neurofibromatosis, underwent successful surgical removal of all tumors.
Area of Science:
- Neurology
- Pediatric Oncology
- Neurosurgery
Background:
- Multiple meningiomas are rare tumors, typically occurring in adults.
- Neurofibromatosis is a known risk factor for developing multiple meningiomas.
- Simultaneous intracranial, intraorbital, and spinal meningiomas are exceptionally uncommon.
Observation:
- A 4-year, 5-month-old boy presented with multiple meningiomas.
- Lesions were identified in the intracranial, intraorbital, and spinal compartments.
- The patient had no history of neurofibromatosis.
Findings:
- All identified meningioma lesions were surgically excised.
- Histological examination confirmed the diagnosis of meningiomas for all excised lesions.
- This case represents the youngest reported patient with multiple meningiomas unrelated to neurofibromatosis.
Implications:
- Highlights the possibility of multiple meningiomas in pediatric patients without genetic predisposition.
- Emphasizes the importance of thorough diagnostic evaluation for pediatric patients presenting with central nervous system or spinal tumors.
- Contributes to the understanding of atypical meningioma presentations and their management in young children.