首页> 美国卫生研究院文献>Annals of Laboratory Medicine >Detection of RUNX1-MECOM Fusion Gene and t(3;21) in a Very Elderly Patient Having Acute Myeloid Leukemia with Myelodysplasia-Related Changes
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Detection of RUNX1-MECOM Fusion Gene and t(3;21) in a Very Elderly Patient Having Acute Myeloid Leukemia with Myelodysplasia-Related Changes

机译:RUNX1-MECOM融合基因和t(3; 21)在患有骨髓增生异常相关变化的急性老年白血病中的检测

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摘要

An 87-yr-old woman was diagnosed with AML with myelodysplasia-related changes (AML-MRC). The initial complete blood count showed Hb level of 5.9 g/dL, platelet counts of 27×109/L, and white blood cell counts of 85.33×109/L with 55% blasts. Peripheral blood samples were used in all the tests, as bone marrow examination could not be performed because of the patient's extremely advanced age and poor general health condition. Flow cytometric analysis, chromosome analysis, FISH, and reverse transcriptase-PCR (RT-PCR) results indicated AML-MRC resulting from t(3;21) with the RUNX1-MECOM fusion gene. To our knowledge, this is the second most elderly de novo AML patient associated with t(3;21) to be reported.
机译:一名87岁的女性被诊断出患有与发育异常相关的AML(AML-MRC)。最初的全血细胞计数显示Hb水平为5.9 g / dL,血小板计数为27×10 9 / L,白细胞计数为85.33×10 9 / L 55%爆炸。所有测试都使用了外周血样本,因为由于患者的年龄极高且总体健康状况较差,因此无法进行骨髓检查。流式细胞仪分析,染色体分析,FISH和逆转录酶PCR(RT-PCR)结果表明AML-MRC是由t(3; 21)与RUNX1-MECOM融合基因产生的。据我们所知,这是与t(3; 21)相关的第二大最老的新生AML患者。

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