Hemangiopericytoma of soft tissue is a controversial pathologic entity. The
relative nonspecificity of the characteristic branching capillary pattern
and cytologic features of the constituent cells, in addition to the lack of
a distinct immunohistochemical staining profile, has resulted in uncertain
ty and a lack of consensus regarding this subgroup of tumors. Notwithstandi
ng the doubt surrounding this entity, a morphologically unique variant, des
ignated lipomatous hemangiopericytoma, was reported in 1995. To our knowled
ge, there have been no further reports of these tumors since the original d
escription. We describe a lipomatous hemangiopericytoma that arose within t
he thigh of a 41-year-old woman. The tumor presented as a slowly enlarging,
minimally tender, pulsatile mass. The tumor was completely excised and was
found to be composed of an admixture of typical hemangiopericytoma and pre
dominantly mature adipose tissue. Unlike previous descriptions of this enti
ty, the current example exhibited a full range of adipocyte differentiation
, including many multivacuolated adipocytes of variable size with character
istic nuclear scalloping (lipoblast-like cells). The mitotic count was less
than 2 per 10 high-power fields examined. The clinical course has been ben
ign during the short follow-up period. We discuss the pathologic features,
including the immunohistochemical staining profile and ultrastructural appe
arance of this distinctive tumor, and briefly discuss the relationship betw
een hemangiopericytoma and solitary fibrous tumor of soft tissue, a neoplas
m with many clinical and pathologic similarities.