Sclerosing epithelioid fibrosarcoma is a rare and slowly growing variant of
fibrosarcoma occurring in adults. Its carcinomatous and/or hemangiopericyt
omatous patterns may mislead to many different tumors. These differential d
iagnoses are generally ruled out by the clinical data, the morphology and t
he immunohistochemical study. We report two typical cases of this fibrosarc
oma and we highlight the different criterias which are indispensable to mak
e the diagnosis. The very slow course of this disease goes along with a ver
y low proliferative rate, but an accumulation of p53 by immunohistochemical
is paradoxically always founds, even though this accumulation is more ofte
n found in highly aggressive sarcomas.