Myxofibrosarcoma is recognized as a malignant neoplasm of fibroblastic origin
with increased prevalence in the elderly, presenting as nodules or tumors that
may extend to the dermis and skeletal muscle, preferably in the lower limbs.
Histologically it is characterized by a proliferation of spindle cells in a
myxoid stroma. Myxofibrosarcoma has a high potential for local recurrence and
metastasis, mainly when it presents a high or intermediate histological grade.
We report the case of an eighty-four year old patient with a difficult diagnosis
of a highly aggressive tumor.