SPTCL is a rare T-cell lymphoma recognized by the new World Health Organization (WHO)-European Organization for Research and Treatment of Cancer (EORTC) classification for cutaneous lymphomas.[2] Lymphomas expressing TCR - αβ which is normally CD8 + and CD56 –, are restricted to the subcutaneous tissue and often run an indolent course. Here, NCAM1 is linked to subcutaneous panniculitis-like T-cell lymphoma.