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首页> 外文期刊>Annals of Clinical and Laboratory Science: Official Journal of the Association of Clinical Scientists >Presence of Additional Cytogenetic Abnormality of t(1;15) at Diagnosis of Chronic Myelogenous Leukemia-Chronic Phase
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Presence of Additional Cytogenetic Abnormality of t(1;15) at Diagnosis of Chronic Myelogenous Leukemia-Chronic Phase

机译:在慢性髓性白血病 - 慢性期诊断中存在额外的细胞遗传学异常的细胞遗传学异常

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摘要

At diagnosis, fewer than 10% of chronic myelogenous leukemia (CML) patients have additional cytogenetic abnormalities (ACAs), which are frequently found in transformation to blast crisis. We report a case of CML-chronic phase (CML-CP) that showed t(1;15) at diagnosis. A 64-year-old man presented with sustained leukocytosis and thrombocytosis. His bone marrow (BM) was hypercellular with 2.5% blasts and BCR-ABL1 rearrangement. The karyotype in the BM was 46, XY, t(1;15)(q32;p13), t(9;22)(q34;q11.2)[20], while the karyotype in the peripheral blood was 46, XY[20]. This is the first report on the presence of t(1;15) at diagnosis of CML-CP, and its clinical significance remains unclear.
机译:在诊断中,少于10%的慢性髓性白血病(CML)患者具有额外的细胞遗传学异常(ACAS),其经常被发现在转型中以进行爆炸危机。 我们报告了CML-慢性阶段(CML-CP)的情况,显示在诊断时T(1; 15)。 一名64岁男子患有持续白细胞增多和血小伤症。 他的骨髓(BM)是高髓质,BCR和BCR-ABL1重排。 BM中的核型为46,XY,T(1; 15)(Q32; P13),T(9; 22)(Q34; Q11.2)[20],而周围血液中的核型为46,XY [20]。 这是关于CML-CP诊断诊断下存在T(1; 15)的第一个报告,其临床意义尚不清楚。

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