摘要
对33例15岁以下急性非淋巴细胞白血病患者进行了细胞遗传学研究,21例(63.6%)有获得性染色体异常。15例为t(8;21),主要属M_2亚型。2例检出近四倍体克隆,皆属M_6.21三体,1q三体,t(15;17)和复杂异常各1例。前两者属M_2,皆由骨髓增生异常综合征演变而来,后两者分属M_3和M_5。
Cytogenetic studies were performed on 33 children with ANLL under the age of 15. In 21 of them (63.6%) acquired chromosomal abnormalities were observed. 15 cases showed t (8; 21) and they belonged mostly to M2 morphologically. A near-tetraploid clone was detected in 2 patients with M6. Each of the four cases had 21 trisomy, lq trisomy, t (15; 17) and complicated abnormality respectively. The first two of them belonged to M2, which developed from myelodysplastic syndrome, while the latter two belonged to M3 and M5 respectively.
出处
《同济医科大学学报》
CSCD
北大核心
1989年第A01期9-11,73,共3页
Acta Universitatis Medicinae Tongji
关键词
白血病
细胞遗传学
染色体
儿童
acute nonlymphocytic leukemia
myelodysplastic syndrome
cyto-genetics
chromosomes