Meningeal hemangiopericytoma (MI-IP) is extremely rare in childhood. Mean a
ge at diagnosis is between 38 and 43 years. We present an 8-year-old boy wi
th MHP of the middle cranial fossa. Imaging findings were indistinguishable
from an aggressive bone tumor such as Ewing's sarcoma. Imaging findings ar
e presented and discussed. Our case indicates that MHP should be considered
in the differential diagnosis of skull-base tumors despite the fact that M
HP is extremely rare in childhood.