Arican Ö.Önver N.Özpuyan F.2024-06-122024-06-1220101300-0330https://hdl.handle.net/20.500.14551/17343Cutaneous lymphomas are rare dermatological disorders and usually thought to be in extranodal non-Hodgkin lymphoma group. Cutaneous B-cell lymphoma (CBCL) is characterized with proliferation of monoclonal B lymphocytes and localized only to the skin for a long time. Primary CBCLs constitute less than 25% of all cutaneous lymphomas. Primary cutaneous follicule center cell lymphoma (PCFCCL) is the tumour of neoplastic follicule center cells. In all types of CBCLs, red-brown colored nodules and tumors are mostly encountered and plaque lesions are rarely seen. We present here, a 38-year-old man diagnosed with PCFCCL because it rarely seen and to emphasize the importance of early diagnosis in long-termed resistant lesions. Copyright © 2010 by Türkiye Klinikleri.trinfo:eu-repo/semantics/closedAccessB-Cell Lymphoma; Follicular Lymphoma; Primary Cutaneous Anaplastic Large Cell LymphomaAdult; Article; B Lymphocyte; Case Report; Cell Proliferation; Cutaneous B Cell Lymphoma; Early Diagnosis; Human; Male; Nonhodgkin Lymphoma; Primary Cutaneous Follicle Center Cell Lymphoma; Rare Disease; Skin Lymphoma; Skin NoduleArticle20140452-s2.0-77953369020Q4