Berger R, Le Coniat M, Vecchione D, Derré J, Chen S J
Laboratoire de Cytogénétique, Unité INSERM U. 301, Hôpital Saint-Louis, Paris, France.
Cancer Genet Cytogenet. 1990 Jan;44(1):69-75. doi: 10.1016/0165-4608(90)90199-k.
Cytogenetic studies on 44 patients with T-cell acute lymphoblastic leukemia (ALL) were reported. The incidence of leukemia without detectable chromosomal changes was 25%. Hyperdiploidy with more than 50 chromosomes was found in only one patient. Previously described nonrandom abnormalities like 6q-, 9p-, and 12p- were observed, and it was confirmed that they are not specific for a particular type of ALL. The incidence of chromosomal rearrangements on chromosomes 7 and 14 where the T-cell receptor gene loci are located was 36% of those with abnormal karyotypes and 27% of the total. This was clearly different from the frequency of rearrangements of these bands found in T-cell lymphoma. Finally, a rearrangement on bands 11q14-q21 was detected in five cases.
报告了对44例T细胞急性淋巴细胞白血病(ALL)患者的细胞遗传学研究。未检测到染色体变化的白血病发生率为25%。仅在1例患者中发现了具有超过50条染色体的超二倍体。观察到先前描述的非随机异常,如6q-、9p-和12p-,并证实它们并非特定类型ALL所特有。T细胞受体基因位点所在的7号和14号染色体上的染色体重排发生率在核型异常患者中为36%,在所有患者中为27%。这与T细胞淋巴瘤中这些带的重排频率明显不同。最后,在5例病例中检测到11q14-q21带的重排。