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Rapidly Enlarging Pediatric Cortical Ependymoma
Kouji Yamasaki1, Kiyotaka Yokogami1, Shinji Yamashita1
1Department of Neurosurgery, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Pediatric supratentorial cortical ependymomas are rare but can rapidly grow. Early diagnosis and vigilant follow-up are crucial for managing these brain tumors in children.
Area of Science:
- Pediatric Neurology
- Neuro-oncology
- Neuroradiology
Background:
- Supratentorial cortical ependymomas are exceptionally rare in pediatric patients.
- Seizures are a common presenting symptom of pediatric brain tumors.
Observation:
- A 10-year-old boy presented with generalized seizures due to a rapidly growing supratentorial cortical ependymoma.
- Initial MRI at age 5 showed a small lesion with no change after 2 years, but a large tumor developed by age 10.
Findings:
- Histopathological diagnosis confirmed ependymoma.
- Complete tumor resection resulted in no neurological deficits.
- The tumor demonstrated significant growth over a 3-year period.
Implications:
- Cortical ependymoma should be considered in the differential diagnosis of pediatric cortical mass lesions presenting with seizures.
- Continuous monitoring is recommended for pediatric patients with cortical lesions, even if asymptomatic, due to potential tumor progression.
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