Abromowitch M, Williams D L, Melvin S L, Stass S
Br J Haematol. 1984 Mar;56(3):409-16. doi: 10.1111/j.1365-2141.1984.tb03971.x.
This case study provides evidence for clonal evolution in pre-B-cell leukaemia. At diagnosis, the lymphoblasts from a 3-year-old boy were morphologically subtyped as L1 (French-American-British classification). Their immunophenotype was CALLA+, CIgM+, SIg-, TdT+, and the karyotype was pseudodiploid with a 1;19 translocation. Striking shifts were apparent when the child relapsed 16 months later. The morphologic subtype had changed to L3, CALLA and TdT had disappeared, and a consistent karyotype was lacking. The modal chromosome number had increased through clonal evolution to 85, the 1;19 translocation was retained, and a new marker, a 14q+ (partial duplication) appeared and was present in a majority of cells. These cytogenetic findings are characteristic of a transforming state. However, despite the loss of TdT, the appearance of classic L3 morphology and the acquisition of a 14q+ marker, the cells retained a predominantly pre-B phenotype.
本病例研究为前B细胞白血病的克隆进化提供了证据。诊断时,一名3岁男孩的淋巴母细胞在形态学上被归类为L1型(法美英分类法)。其免疫表型为CALLA阳性、胞浆IgM阳性、表面Ig阴性、末端脱氧核苷酸转移酶阳性,核型为假二倍体,伴有1;19易位。16个月后患儿复发时出现了显著变化。形态学亚型已变为L3型,CALLA和末端脱氧核苷酸转移酶消失,且缺乏一致的核型。通过克隆进化,众数染色体数目增加到85条,1;19易位得以保留,一个新的标记物14q +(部分重复)出现并存在于大多数细胞中。这些细胞遗传学发现是转化状态的特征。然而,尽管末端脱氧核苷酸转移酶缺失、出现了典型的L3形态且获得了14q +标记物,但细胞仍主要保留前B表型。