The solitary fibrous tumor (SFT) is a rare tumor that most commonly arises
in the pleura. Recent evidence has indicated that this tumor originates fro
m mesenchymal, probably fibroblastic, cells and is not restricted to the pl
eura. However, its occurrence in the female genital tract is extremely rare
. We report a case of primary SFT that originated from the vagina in a 34-y
ear-old female. It was a pedunculated polypoid tumor and occurred at the si
te of scar tissue, caused by laceration during her last labor 7 years previ
ously. Histologically, the tumor was predominantly composed of a random pro
liferation of spindle cells, intimately admixed with collagen. Immunohistoc
hemically, the cells were strongly positive for CD34, vimentin and bcl-2, b
ut were negative for S-100 protein, neuron-specific enolase, smooth muscle
actin, desmin, CD68, cytokeratins and epithelial membrane antigen. To the b
est of our knowledge, this is the first reported case of a primary vaginal
SFT in the English literature. Our report suggests to include SFT in the di
fferential diagnosis of a spindle cell neoplasm originating from the vagina
.