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%). Altho
ugh there are numerous case reports in the literature, no firm conclus
ions can be drawn. For this report we accumulated, reviewed, and analy
zed reports in the literature from 1960-93. METHODS A total of 318 pat
ients with meningioma were managed in King Faisal Specialist Hospital
and Research Centre from 1981-93. Nine of these patients (2.8%) were c
hildren aged 16 years or less. These cases were analyzed retrospective
ly with regard to age, sex, clinical presentation, radiologic findings
, pathologic findings, management, and outcome. RESULTS Childhood meni
ngioma represented 2.8% of all meningioma cases and 2.2% of all centra
l nervous system tumors seen in children. There were six males and thr
ee females. The average age at presentation was 10.1 years (range 1-16
years). There were four cases of meningioma in the orbit and 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 frequ
ently seen. CONCLUSION Meningioma is rare in children and males are af
fected more than females. Tumor locations that are rare in adults are
more common in children. The meningothelial type is most frequently se
en. 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 effor
t 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 psyc
hologic complications.