Myxofibrosarcoma, also known as a myxoid variant of malignant fibrous histi
ocytoma, is one of the most common sarcomas in the extremities of elderly p
eople and is characterized by a high frequency of local recurrence. We repo
rt a case of myxofibrosarcoma, intermediate grade, involving the thigh alon
g the fascial plane and between the muscles without the formation of an app
arent nodular lesion. On microscopic examination, the tumor lacked areas of
necrosis and pronounced cellular pleomorphism, but it was highly cellular
with proliferation of spindle cells which contained large elongated, hyperc
hromatic and irregularly shaped nuclei, slightly eosinophilic cytoplasm and
indistinct cell margins, arranged in both interlacing fascicles and a stor
iform pattern. Immunohistochemically, many of the tumor cells showed intens
e reactivity to vimentin and CD34. More than 20% of the cells were positive
for p53 protein and the MIB-1 labeling index was similar to 30%. Desmin, a
lpha-smooth muscle actin, muscle-specific actin, S-100 protein, cytokeratin
, epithelial membrane antigen, bcl-2 protein and neurofilament were negativ
e. The absence of a discrete mass lesion and diffuse infiltrative nature pr
ecluded early recognition of tumor. Seven years after hindquarter amputatio
n, the patient has been alive without evidence of local recurrence or dista
nt metastasis. This case indicates that myxofibrosarcoma can demonstrate a
highly infiltrative growth pattern. It is possible that this infiltrative n
ature is associated with a high rate of local recurrence of the tumor. A ca
reful radiological examination of the extension of the tumor prior to surge
ry is mandatory considering the infiltrative nature of myxofibrosarcoma.