alexa Meningioma in children: a report of nine cases and a review of the literature.
Oncology

Oncology

Journal of Brain Tumors & Neurooncology

Author(s): Sheikh BY, Siqueira E, Dayel F

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Abstract BACKGROUND: Meningioma is a common tumor of the central nervous system in adults, accounting for 10\%-20\% of all primary intracranial tumors. It is rare in children, with an incidence of 2.19\% (0.85\%-2.3\%). Although there are numerous case reports in the literature, no firm conclusions can be drawn. For this report we accumulated, reviewed, and analyzed reports in the literature from 1960-93. METHODS: A total of 318 patients with meningioma were managed in King Faisal Specialist Hospital and Research Centre from 1981-93. Nine of these patients (2.8\%) were children aged 16 years or less. These cases were analyzed retrospectively with regard to age, sex, clinical presentation, radiologic finding, pathologic findings, management and outcome. RESULTS: Childhood meningioma represented 2.8\% of all meningioma cases and 2.2\% of all central nervous system tumors seen in children. There were six males and three females. The average age at presentation was 10.1 years (range 1-16 years). There were four cases of meningioma in the orbit an one each in the temporal region, foramen magnum, tentorial region, subfrontal base, sellar region and ethmoidal air sinus. There were two cases of multiple meningioma. Meningothelial meningioma was the type most frequently seen. CONCLUSION: Meningioma is rare in children and males are affected more than females. Tumor locations that are rare in adults are more common in children. The meningothelial type is most frequently seen. Prognosis is poor compared with that in adults, as the tumors tend to grow more rapidly and to a larger size, undergo malignant changes, and have a greater rate of recurrence. Whenever feasible, every effort should be made to achieve total resection of the tumor at the first attempt. If radiation therapy is used in children it should be limited to those who have recurrent tumors so as to minimize organic and psychologic complications.
This article was published in Surg Neurol and referenced in Journal of Brain Tumors & Neurooncology

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