Mitelman F, Nilsson P G, Levan G, Brandt L
Int J Cancer. 1976 Jul 15;18(1):31-8. doi: 10.1002/ijc.2910180106.
Bone-marrow chromosomes were examined with the G-banding technique in 30 patients with acute myeloid leukemia at the time of diagnosis. In 13 of the 30 patients (43%) only normal diploid bone-marrow cells were found, and no deviations from the normal banding pattern could be detected in these cells. In bone-marrow cells of 17 patients (57%), distinct chromosome abnormalities were found; in 10 of the patients only abnormal cells were observed, whereas in 7 of the patients the abnormal cells coexisted with normal diploid cells without any visible chromosome banding abnormality. The results of the detailed analysis of the karyotypic aberrations demonstrated that when chromosome aberrations occurred they were clearly non-random. All patients except two displayed trisomy 8,9 or 21 or monosomy 7. Analysis of cases of acute leukemia from other laboratories indicated that the same consistent pattern of chromosome involvement prevailed in them.
采用G显带技术对30例急性髓系白血病患者诊断时的骨髓染色体进行了检查。30例患者中有13例(43%)仅发现正常二倍体骨髓细胞,这些细胞未检测到与正常带型模式的偏差。在17例患者(57%)的骨髓细胞中发现了明显的染色体异常;10例患者仅观察到异常细胞,而7例患者的异常细胞与正常二倍体细胞共存,且无任何可见的染色体带型异常。核型畸变的详细分析结果表明,当染色体畸变发生时,它们显然是非随机的。除两名患者外,所有患者均表现为8、9或21号染色体三体或7号染色体单体。对其他实验室的急性白血病病例分析表明,它们中也存在相同的一致的染色体受累模式。