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首页> 外文期刊>Annals of hematology >Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia.
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Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia.

机译:分子细胞遗传学发现支持急性髓性白血病的双克隆起源证据。

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摘要

Hematologic malignancies are clonal disorders arising from a single mutated cell. However, the detection of more than one cytogenetically unrelated abnormal clone has occasionally been reported . Cytogenetic biclonality has rarely been observed in adult acute myeloid leukemia (AML); in none of the cases reported in literature has a molecular cytogenetic analysis been performed [1, 5]. We report a case of adult AML-M2 at diagnosis with biclonal cytogenetic abnormalities represented by two novel translocations. The first clone showed a translocation t(l;2)(p23;p21), while in the second clone, we observed an unbalanced t(ll;12)(q!3;pl3).
机译:血液系统恶性肿瘤是由单个突变细胞引起的克隆性疾病。但是,偶尔也有报道发现了一种以上与细胞遗传学无关的异常克隆。在成年急性髓细胞性白血病(AML)中很少观察到细胞遗传学的克隆性;在文献报道的任何案例中,都没有进行分子细胞遗传学分析[1,5]。我们报告了一例成人AML-M2的诊断为由两个新的易位代表的双克隆细胞遗传学异常。第一个克隆显示出易位t(1; 2)(p23; p21),而在第二个克隆中,我们观察到不平衡的t(11; 12)(q!3; pl3)。

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