“…Clinically, atrophic DFSP lesion is centrally depressed, whereas classical DFSP has a protuberant presentation; however, both variants show similar histological and immunohistochemical features, such as fibrohistocytic cell proliferation [ 14 , 15 ], CD34, and vimentin expression, and lack of staining with CD44, S100 protein or XIIIa [ 1 , 16 ]. Both variants also demonstrate COL1A1/PDGFB gene rearrangement fusion [ 2 , 16 ].…”