Yumura-Yagi K, Fujinami A, Hara J, Ishihara S, Kawa-Ha K
Department of Pediatrics, Osaka University Hospital, Japan.
Cancer. 1989 Jun 1;63(11):2130-3. doi: 10.1002/1097-0142(19890601)63:11<2130::aid-cncr2820631110>3.0.co;2-9.
A 2-year-old boy with B-lineage non-Hodgkin's lymphoma is described. He presented with growing skin tumors on his head, and biopsy specimens showed a malignant lymphoma of diffuse lymphoblastic type. Sixty-four percent of bone marrow cells were replaced with lymphoblasts, and they expressed B-lineage markers (CD19 and HLA/DR). Southern blot analysis demonstrated immunoglobulin heavy chain gene rearrangements (two rearranged and one germline) with the germline configuration of the T-cell receptor beta chain gene. Ten months later he relapsed with blasts of M5 morphologic type and a myeloid phenotype with the germline configuration of the immunoglobulin genes. During the next 2 months, myeloid blasts with immunoglobulin gene rearrangement which was identically rearranged with one of the two rearranged bands detected at diagnosis appeared. The most likely explanation for these findings is that initially the patient seemed to have at least two different clones of blasts, and clonal selections occurred during the treatments.
本文描述了一名患有B系非霍奇金淋巴瘤的2岁男孩。他因头部不断生长的皮肤肿瘤就诊,活检标本显示为弥漫性淋巴细胞型恶性淋巴瘤。64%的骨髓细胞被淋巴母细胞取代,且这些细胞表达B系标志物(CD19和HLA/DR)。Southern印迹分析显示免疫球蛋白重链基因重排(两条重排带和一条胚系带),而T细胞受体β链基因呈胚系构型。10个月后,他复发,表现为M5形态学类型的原始细胞和具有免疫球蛋白基因胚系构型的髓系表型。在接下来的2个月里,出现了具有免疫球蛋白基因重排的髓系原始细胞,其重排与诊断时检测到的两条重排带之一完全相同。对这些发现最可能的解释是,最初患者似乎至少有两个不同的原始细胞克隆,且在治疗过程中发生了克隆选择。