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Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.

机译:三体性8是急性髓性白血病和骨髓增生异常综合征中唯一的染色体畸变。

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摘要

Trisomy 8 as the sole abnormality is the most common karyotypic finding in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), occurring in approximately 5% and 10% of the cytogenetically abnormal cases, respectively. However, despite the high frequency of +8, much remains to be elucidated as regards its epidemiology, etiology, clinical impact, association with other chromosomal abnormalities, cell of origin, and functional and pathogenetic consequences. Here, we summarize and review these various aspects of trisomy 8, focusing on AMLs and MDS harboring this abnormality as a single change.
机译:在急性髓细胞性白血病(AML)和骨髓增生异常综合症(MDS)中,三体性8是唯一的异常,是最常见的核型学发现,分别发生在约5%和10%的细胞遗传学异常病例中。然而,尽管+8的发生频率很高,但是关于其流行病学,病因,临床影响,与其他染色体异常的关联,起源细胞以及功能和致病性后果,还有许多事情尚待阐明。在这里,我们总结并回顾了三体性8的各个方面,重点是将这种异常作为单个变化保留的AML和MDS。

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