Pheochromocytoma is rare in children. A wide varieties of lesions are obser
ved and diagnosis, often made late, is based on urinary catecholamine assay
. Magnetic resonance imaging provides the best morphological information. T
he disease is usually benign and prognosis is good.
Familial forms of pheochromocytoma and pheochromocytoma associated with isc
hemia-induced bone lesions must be emphasized.