Aims: Dermatofibrosarcoma protuberans (DFSP) is a distinctive cutaneou
s spindle cell neoplasm that invariably infiltrates the subcutaneous t
issue. Other reports have suggested that exceptional cases of DFSP may
be confined to the subcutaneous tissue and lack dermal involvement. W
e wish to confirm this observation by describing cases of a rare varia
nt of DFSP confined to the subcutaneous tissue, and analyse possible h
istogenetic implications, Methods and results: Three cases of DFSP loc
ated in the subcutaneous tissue are reported, Multiple step sections d
emonstrated the lack of dermal involvement in two of them, whereas the
third case infiltrated the dermis at the junction with the subcutis m
inimally in one of five blocks, Immunohistochemical studies using a ba
ttery of monoclonal antibodies were performed, All the tumours stained
strongly for vimentin and CD34. Conclusions: Because of the lack of d
ermal involvement in two cases and only minimal dermal involvement in
one case, we called this variant deep DFSP. Except for deep setting of
the tumour, deep DFSP is distinguishable from typical DFSP clinically
, histologically and immunohistochemically. The existence of deep DFSP
provides evidence that specific structures of the skin may be not inv
olved in this tumour's histogenesis.