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首页> 外文期刊>Pathology Research and Practice >Molecular characterization of complex chromosomal rearrangement: First report of novel t(7;12) (q11;q22) as part of a complex karyotype in de novo AML-M2 case
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Molecular characterization of complex chromosomal rearrangement: First report of novel t(7;12) (q11;q22) as part of a complex karyotype in de novo AML-M2 case

机译:复杂染色体重排的分子表征:新型t(7; 12)(q11; q22)作为从头AML-M2病例中复杂核型的一部分的首次报道

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摘要

The strong association of diagnostic karyotype with clinical outcome has made cytogenetics one of the most valuable diagnostic and prognostic tools for acute myeloid leukemia (AML) till today. Complex chromosomal findings are reported to be seen in nearly 10-15% of adult AMLs and are generally associated with poor outcome. In the current report, we present the results of hematologic, immunophenotypic, cytogenetic, chromosomal microarray and molecular analyses of a 60-year-old female patient diagnosed with AML-M2. Cytogenetic analysis revealed complex chromosomal findings involving seven different chromosomes. However, cytogenetic analyses were not able to precisely unveil all karyotypic changes, hence chromosomal microarray was used for further characterization. The most interesting observation was identification of a t(7;12) (q11;q22) as part of this complex karyotype. To the best of our knowledge, this is the first report of identification of novel t(7;12) (q11;q22) as part of a complex karyotype in de nova AML-M2. (C) 2014 Elsevier GmbH. All rights reserved.
机译:迄今为止,诊断性核型与临床结果之间的紧密联系使细胞遗传学成为急性髓细胞性白血病(AML)最有价值的诊断和预后工具之一。据报道,在成人AML中有近10-15%可以看到复杂的染色体发现,并且通常与不良结果相关。在本报告中,我们介绍了60岁诊断为AML-M2的女性患者的血液学,免疫表型,细胞遗传学,染色体微阵列和分子分析的结果。细胞遗传学分析揭示了涉及七个不同染色体的复杂染色体发现。然而,细胞遗传学分析不能准确揭示所有核型变化,因此使用染色体微阵列进行进一步表征。最有趣的观察是鉴定t(7; 12)(q11; q22)作为这种复杂核型的一部分。据我们所知,这是首次鉴定新型t(7; 12)(q11; q22)作为新星AML-M2中复杂核型的一部分。 (C)2014 Elsevier GmbH。版权所有。

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