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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Novel Cytogenetic Aberrations in a Patient of Chronic Myeloid Leukemia with Blast Crisis
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Novel Cytogenetic Aberrations in a Patient of Chronic Myeloid Leukemia with Blast Crisis

机译:爆发性慢性粒细胞白血病患者的新型细胞遗传学畸变

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Chronic myeloid leukaemia (CML) is a clonal haematological disease which is characterized by a diagnostic karyotypic abnormality t (9;22)(q34;q11) called as Philadelphia (Ph) chromosome. Occurrence of additional chromosomal abnormalities besides the Ph chromosome is defined as clonal evolution (CE) and considered to be a marker of disease progression. A 67-year-old male who was initially evaluated at a private hospital where a diagnosis of acute promyelocytic leukaemia was made on bone marrow aspirate with ambiguous RT-PCR report referred to our centre for further evaluation and treatment. On conventional karyotyping, Ph chromosome along with translocations t(5;13)(q12;p13), t(15;20)(q22;p13) and monosomy 13 was observed in all 20 metaphases. A final diagnosis of CML-myeloid blast crisis with complex cytogenetics was made. Patient succumbed to death within one month of initiation of imatinib therapy.
机译:慢性粒细胞白血病(CML)是一种克隆性血液病,其特征在于诊断核型异常t(9; 22)(q34; q11),称为费城(Ph)染色体。除Ph染色体外,其他染色体异常的发生被定义为克隆进化(CE),被认为是疾病进展的标志。最初在一家私立医院接受评估的67岁男性,当时诊断为急性早幼粒细胞白血病,并通过含糊的RT-PCR报告诊断出骨髓早幼白血病,转诊至我们中心进行进一步评估和治疗。在常规核型分析中,在所有20个中期都观察到Ph染色体以及易位t(5; 13)(q12; p13),t(15; 20)(q22; p13)和13号单体。最终诊断为具有复杂细胞遗传学的CML髓母细胞瘟疫。患者在伊马替尼治疗开始后一个月内死亡。

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