Mestel D Sebastian, Beyer M, Steinhoff M, Sterry W, Assaf C
Department of Dermatology and Allergy, Skin Cancer Center, Charité-Universitaetsmedizin, Berlin, Germany.
G Ital Dermatol Venereol. 2008 Dec;143(6):395-408.
Primary cutaneous T-cell lymphomas (PCLs) mycosis fungoides (MF) and Sézary syndrome (Ss) belong to the group of non-Hodgkin lymphomas (NHL), which are characterized by clonally proliferating CD4+ cells localized in the skin. Although there already exist many conventional skin-directed and systemic cytotoxic treatment options, in long-term only a transient remission without curative results will be reached in most cases. The aim of this article was to present actual assumed treatment modalities, as well as new therapeutic strategies which passed already through clinical trials showing promising results in the treatment of PCLs.
原发性皮肤T细胞淋巴瘤(PCL)蕈样肉芽肿(MF)和塞扎里综合征(SS)属于非霍奇金淋巴瘤(NHL)组,其特征为皮肤中克隆性增殖的CD4 +细胞。尽管已经存在许多传统的皮肤定向和全身细胞毒性治疗选择,但在大多数情况下,长期来看仅能达到短暂缓解而无治愈效果。本文的目的是介绍目前假定的治疗方式以及已经通过临床试验的新治疗策略,这些策略在PCL治疗中显示出有希望的结果。