Angiomatoid fibrous histiocytoma is an unusual tumor, affecting primarily y
oung adults who develop local disease with favorable prognosis. This contra
sts with the aggressive natural history of malignant fibrohistiocytoma. We
report case of a 9-year-old girl who presented with a tumor mass of soft ti
ssues with an unusual deep location, thereby with non distinctive clinical
features. Surgical treatment was performed.