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Meningioangiomatosis in a 5-year-old boy presenting with intractable seizures
George A Alexiou1, Maria Moschovi, Kalliopi Stefanaki
1Department of Neurosurgery, First Department of Pediatrics, University of Athens, Athens, Greece. alexiougrg@yahoo.gr
Abstract:
A 5-year-old boy with a history of epilepsy underwent brain magnetic resonance imaging (MRI) because of an increase in seizure frequency. Brain MRI demonstrated a left frontal lesion. The patient was operated upon, and gross total excision was performed. The histological diagnosis was meningioangiomatosis. On follow-up examination 10 years later, the patient was free of seizures and without any evidence of tumor recurrence. Meningioangiomatosis is a rare benign hamartomatous lesion that is associated with seizures. Complete excision is associated with favorable long-term outcome. The novelty of the present case is the young age of the child at presentation and the curative role of surgery considering the long-term follow-up.
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