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A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case

机译:费城阳性慢性粒细胞白血病病例中的新型细胞遗传学异常r(7)(:: p11.2-> q36.3::)

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The so-calledPhiladelphia(Ph) chromosome is present in more than 90% of chronic myeloid leukemia (CML) cases. It results in juxtaposition of the 5' part of the BCR gene on chromosome 22 and the 3' part of the ABL1 gene on chromosome 9. An additional acquired monosomy 7 or deletion of 7q is associated with poor prognosis in a variety of myeloid disorders. Here we report a novel Ph chromosome positive CML case with a ring chromosome 7 [r(7)]. Immunophenotyping was compatible with CML, although 4.5% of total leucocytes appeared like acute myelogeneous leukemia (AML) subtype M2. The r(7) was characterized in detail by array-proven multicolor banding (aMCB), the latter being of enormous significance to characterize breakpoint regions in detail. Underlying mechanisms and prognostic are discussed, as ring chromosomes are rare cytogenetic abnormalities in hematopoietic malignancies.
机译:在超过90%的慢性粒细胞白血病(CML)病例中存在所谓的费城染色体。它导致BCR基因5'部分在22号染色体上并置,而ABL1基因3'在9号染色体上并置。额外的获得性7号染色体或7q缺失与多种髓样疾病的不良预后有关。在这里,我们报告了一个新的Ph染色体阳性CML病例,其环形染色体7 [r(7)]。免疫分型与CML兼容,尽管总白细胞的4.5%看起来像是急性骨髓性白血病(AML)M2亚型。 r(7)的特征是经过阵列验证的多色条带(aMCB),后者对详细描述断点区域具有重要意义。讨论了潜在的机制和预后,因为环形染色体是造血系统恶性肿瘤中罕见的细胞遗传学异常。

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