Yoshizawa Naho, Yagi Hiroaki, Horibe Takahiro, Takigawa Masahiro, Sugiura Makoto
Department of Dermatology, Shizuoka Municipal Shimizu Hospital, 1231 Miyakami Shimizu, Shizuoka 424-8636, Japan.
Eur J Dermatol. 2007 Sep-Oct;17(5):441-2. doi: 10.1684/ejd.2007.0245. Epub 2007 Aug 2.
Primary cutaneous aggressive epidermotropic CD8(+) T-cell lymphoma (CD8(+)TCL) is an extremely rare entity with distinct clinicopathological features. While the CD15 antigen is typically associated with classic Hodgkin's lymphoma, aggressive peripheral T-cell lymphomas, including advanced stage cutaneous T-cell lymphomas, rarely express this molecule. We report a case of primary cutaneous aggressive epidermotropic CD8(+)TCL, in which lymphoma cells are CD15(+)CD30(-) with a medium-to-large pleomorphic phenotype. Although the functional characteristics of CD15 expression in the cutaneous lymphomas are not fully understood, the poor prognosis of primary cutaneous aggressive epidermotropic CD8(+)TCL might be associated with the presence of this molecule in our case.
原发性皮肤侵袭性亲表皮性CD8(+) T细胞淋巴瘤(CD8(+)TCL)是一种极为罕见的疾病,具有独特的临床病理特征。虽然CD15抗原通常与经典霍奇金淋巴瘤相关,但侵袭性外周T细胞淋巴瘤,包括晚期皮肤T细胞淋巴瘤,很少表达该分子。我们报告一例原发性皮肤侵袭性亲表皮性CD8(+)TCL,其中淋巴瘤细胞为CD15(+)CD30(-),具有中到大的多形性表型。虽然皮肤淋巴瘤中CD15表达的功能特征尚未完全明确,但在我们的病例中,原发性皮肤侵袭性亲表皮性CD8(+)TCL的不良预后可能与该分子的存在有关。