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儿童急性淋巴细胞白血病的细胞遗传学异常

Cytogenetic abnormalities in childhood acute lymphoblastic leukemia.

作者信息

Micallef-Eynaud P D, Eden O B, Grace E, Ellis P M

机构信息

Royal Hospital for Sick Children, Edinburgh, Scotland, United Kingdom.

出版信息

Pediatr Hematol Oncol. 1993 Jan-Mar;10(1):25-30. doi: 10.3109/08880019309016524.

Abstract

A review of the cytogenetic analyses of a cohort of unselected patients with acute lymphoblastic leukemia from a single institution (1981-1989) confirmed hyperdiploidy > 50 as a favorable prognostic feature and pseudodiploidy, especially with chromosomal rearrangements, as an adverse one. In the early years of the study, a high incidence of diploid karyotype was identified, but with time (better banding and more intensive search) the incidence has fallen to 7.7%. Many such patients have been shown to be pseudodiploid. Molecular genetic techniques are increasingly identifying clonal abnormalities.

摘要

对来自单一机构的一组未经选择的急性淋巴细胞白血病患者(1981 - 1989年)进行的细胞遗传学分析回顾证实,超二倍体>50是一个良好的预后特征,而假二倍体,尤其是伴有染色体重排的假二倍体,则是不良预后特征。在研究的早期,发现二倍体核型的发生率很高,但随着时间推移(更好的显带技术和更深入的检测),该发生率已降至7.7%。许多这类患者已被证明是假二倍体。分子遗传学技术越来越多地识别出克隆性异常。

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