“…Given the findings on imaging, the differential is broad but from a clinical, pathologic, and molecular standpoint, LLTs have similarities to low-grade myxofibrosarcoma (similar morphological appearance, but intact Rb expression and lack of SMA expression argues against this) [15] , cellular angiofibroma (similar morphological appearance, both desmin − CD34 + , but intact Rb and S100 expression argues against this) [14] , [16] , atypical spindle cell lipomatous tumor (both are negative for MDM2 amplification, CD34 + S100 + , but Rb is typically lost in this tumor) [7] , myxoid liposarcoma (both negative for MDM2 amplification and S100 + , although the absence of DDIT3 translocation argues against this) [3] , [9] , [17] , and spindle cell tumors (both SOX10 − CD34 + S100 + , but lacking NTRK expression/gene fusion commonly found in spindle cell tumors makes it unlikely) [18] .…”