Donti E, Falini B, Giuseppe Pelicci P, Venti Donti G, Rosetti A, Martelli M, Grignani F
First Institute of Internal Medicine, University of Perugia, Italy.
Leukemia. 1988 Jan;2(1):41-4.
Two sequential lymph node biopsies taken from a non-Hodgkin lymphoma patient revealed two karyotype abnormalities peculiar to B cell neoplasias: trisomy 12 and t(2;8)(p12;q24) translocation. The first was documented in all cells analyzed, while the second was present in 20% of the metaphases from the first biopsy and in 100% from the second. This suggests that the t(2;8) translocation arose as a secondary karyotypic change. In addition, although immunological characterization of the neoplastic cells disclosed a monoclonal B cell population that expressed immunoglobulin kappa light chains, as usually found in Burkitt's lymphoma with t(2;8) translocation, Southern blot analysis provided evidence of rearrangement in only one kappa chain allele.
从一名非霍奇金淋巴瘤患者身上采集的两份连续淋巴结活检样本显示出两种B细胞肿瘤特有的核型异常:12号染色体三体和t(2;8)(p12;q24)易位。第一种异常在所有分析的细胞中都有记录,而第二种异常在第一次活检的中期细胞中有20%出现,在第二次活检的中期细胞中有100%出现。这表明t(2;8)易位是作为一种继发性核型变化出现的。此外,尽管肿瘤细胞的免疫特征显示出一个表达免疫球蛋白κ轻链的单克隆B细胞群体,这在伴有t(2;8)易位的伯基特淋巴瘤中通常可见,但Southern印迹分析仅提供了一个κ链等位基因重排的证据。