“…In addition, histopathological findings using both HE and IHC staining suggest the diagnosis of PCFCL with the findings of lymphocyte infiltrates on the dermis and subcutaneous forming a follicular/diffuse appearance, while there were no abnormalities found on the epidermis. There are various antibodies that can be used in IHC staining to confirm the diagnosis of PCFCL, such as CD20, PAX5, CD10, BCL2, and BCL6, in which, our case showed positive result for CD-20 antibody [9]. PCFCL is considered as a slow growing subtype of CBCL, with a 95% 5-year survival rate [3], [9], [10].…”