UC San Diego Moores Cancer Center, San Diego, CA, USA.
Cancer J. 2012 Sep-Oct;18(5):439-44. doi: 10.1097/PPO.0b013e31826c57f1.
The cutaneous T-cell lymphomas are a heterogeneous collection of many biologically and clinically distinct cancers. The World Health Organization 2008 reclassification of cutaneous lymphomas delineated provisional entities that were previously classified simply as primary cutaneous peripheral T-cell lymphoma not otherwise specified. Because of the relative rarity of cases, standard treatment recommendations and algorithms are lacking. However, identification of these subtypes is important as they can have vastly different clinical outcomes. Furthermore, cytokine treatments effective in classic mycosis fungoides or Sezary syndrome not only are ineffective, but also may exacerbate certain subtypes. The aim of this review was to summarize the biological bases of the recently defined entities, reinforce the importance of acute clinical/pathologic diagnosis, and propose treatment strategies based on the available data.
皮肤 T 细胞淋巴瘤是一组具有多种生物学和临床特征的异质性癌症。2008 年世界卫生组织对皮肤淋巴瘤的重新分类将以前简单归类为未特指的原发性皮肤外周 T 细胞淋巴瘤的临时实体进行了划分。由于病例相对较少,缺乏标准的治疗建议和方案。然而,确定这些亚型非常重要,因为它们可能具有截然不同的临床结局。此外,在经典蕈样真菌病或 Sezary 综合征中有效的细胞因子治疗不仅无效,而且可能使某些亚型恶化。本综述的目的是总结最近定义的实体的生物学基础,强调急性临床/病理诊断的重要性,并根据现有数据提出治疗策略。