Buckner Carl L, Christiansen Lydia R, Bourgeois Danyel, Lazarchick John J, Lazarchick John
Dept of Pathology & Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Ann Clin Lab Sci. 2007 Summer;37(3):263-7.
Mature T-cell neoplasms are relatively uncommon, accounting for approximately 10% of all non-Hodgkin lymphomas. This category of hematopoietic neoplasms is clinically aggressive and shows a poor response to therapy and shortened survival. The antigen CD20 has long been thought to be a specific marker for B-cell lineage and has been used to help differentiate T-cell and B-cell neoplasms. We present two cases of a rare subset of T-cell leukemia/lymphoma having a unique immunophenotype, both being CD20+. The significance of CD20 antigen in T-cell lymphomas is yet to be determined, but may allow treatment with novel therapeutic agents (eg, rituximab, a recombinant anti-CD20 monoclonal antibody).
成熟T细胞肿瘤相对少见,约占所有非霍奇金淋巴瘤的10%。这类造血系统肿瘤临床侵袭性强,对治疗反应不佳且生存期缩短。长期以来,抗原CD20一直被认为是B细胞系的特异性标志物,并被用于辅助鉴别T细胞和B细胞肿瘤。我们报告了两例具有独特免疫表型的罕见T细胞白血病/淋巴瘤亚型病例,二者均为CD20阳性。CD20抗原在T细胞淋巴瘤中的意义尚待确定,但可能有助于采用新型治疗药物(如利妥昔单抗,一种重组抗CD20单克隆抗体)进行治疗。