Hsu L Y, Greenberg M L, Kohan S, Wittman R
Clin Genet. 1979 Apr;15(4):327-31. doi: 10.1111/j.1399-0004.1979.tb01742.x.
We have identified trisomy 13 in two additional patients with hematologic malignancies involving the hematopoietic stem cell: a 75-year-old female with acute myelocytic leukemia and a 64-year-old female with agnogenic myelofibrosis and myeloid metaplasia. Chromosome analysis of the direct bone-marrow preparation showed 100% of cells with trisomy 13 in the first and 10% of cells in the second. We also previously reported a patient with Ph1 negative chronic myelogenous leukemia in whom 100% of the marrow cells showed an identical trisomy. The probability of finding three such patients in our case material was calculated to be 0.05--0.08, implying that trisomy 13 may be another nonrandom chromosomal aberration associated with malignancies of hematopoietic pluri-potent stem cell.
我们在另外两名涉及造血干细胞的血液系统恶性肿瘤患者中发现了13号染色体三体:一名75岁患有急性髓细胞白血病的女性和一名64岁患有原发性骨髓纤维化和髓样化生的女性。直接骨髓涂片的染色体分析显示,第一名患者100%的细胞存在13号染色体三体,第二名患者则为10%。我们之前还报告过一名Ph1阴性慢性粒细胞白血病患者,其100%的骨髓细胞显示出相同的三体。在我们的病例资料中发现三名此类患者的概率经计算为0.05 - 0.08,这意味着13号染色体三体可能是另一种与造血多能干细胞恶性肿瘤相关的非随机染色体畸变。