Ohtsuki T, Ogawa Y, Izumi T, Hatake K, Miura Y
Department of Internal Medicine, Jichi Medical School, Tochigi-ken, Japan.
Acta Haematol. 1996;96(4):258-61. doi: 10.1159/000203798.
Acute lymphocytic leukemia with mature B-cell phenotype (B-ALL) is a rare type of ALL. Although B-ALL cells commonly have a characteristic chromosomal translocation that includes 8q24 (the location of the c-myc protooncogene), the leukemic cells of the two patients reported in this paper showed normal karyotypes. This finding was confirmed by Southern blot analysis of bone marrow cells in case 1. A c-myc probe was used, and no rearrangement or amplification of c-myc expression was found; B-ALL with the translocation including 8q24 is reported to show high levels of expression of rearranged c-myc. Investigation of anti-Epstein-Barr virus (EBV) antibody revealed that both cases 1 and 2 had a past history of EBV infection. However, at least in case 1, integration of the EBV genomic DNA into the leukemic cells was not detected by the polymerase chain reaction in which specific primers for EBV were employed. The difference in pathophysiology between B-ALL with and without the 8q24 translocation is unclear, however, the prognosis of the two patients with B-ALL with the normal karyotype was as poor as that of B-ALL with the chromosomal translocation.
具有成熟B细胞表型的急性淋巴细胞白血病(B-ALL)是一种罕见的ALL类型。尽管B-ALL细胞通常具有特征性的染色体易位,包括8q24(c-myc原癌基因的位置),但本文报道的两名患者的白血病细胞显示核型正常。病例1骨髓细胞的Southern印迹分析证实了这一发现。使用了c-myc探针,未发现c-myc表达的重排或扩增;据报道,伴有8q24易位的B-ALL显示重排的c-myc表达水平较高。抗爱泼斯坦-巴尔病毒(EBV)抗体检测显示,病例1和病例2既往均有EBV感染史。然而,至少在病例1中,采用EBV特异性引物的聚合酶链反应未检测到EBV基因组DNA整合到白血病细胞中。伴有和不伴有8q24易位的B-ALL之间的病理生理学差异尚不清楚,然而,两名核型正常的B-ALL患者的预后与伴有染色体易位的B-ALL患者一样差。