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在前体B淋巴细胞系急性淋巴细胞白血病中发现的一种非随机染色体异常:dic(9;20)(p1?3;q11)

A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11).

作者信息

Slater R, Smit E, Kroes W, Bellomo M J, Mühlematter D, Harbott J, Behrendt H, Hählen K, Veerman A J, Hagemeijer A

机构信息

Institute of Human Genetics, University of Amsterdam, The Netherlands.

出版信息

Leukemia. 1995 Oct;9(10):1613-9.

PMID:7564498
Abstract

A comparison of cytogenetical data on acute lymphoblastic leukaemia studied at four large European centres has revealed a non-random dicentric chromosome abnormality: dic(9;20) (p1?3;q11) in 10 patients, nine of whom were children. All had early precursor-B lineage ALL, and eight children had a non-standard risk clinical presentation. The origin of the dicentric chromosome was demonstrated using a range of chromosome banding techniques. This was confirmed by FISH using paints and centromeric probes for chromosomes 9 and 20, together with a number of cosmid probes. The follow-up time of these patients is presently too short and the number of patients too few to determine the prognostic significant of this chromosome abnormality.

摘要

对欧洲四个大型中心研究的急性淋巴细胞白血病细胞遗传学数据进行比较后发现了一种非随机的双着丝粒染色体异常

10例患者存在dic(9;20)(p1?3;q11),其中9例为儿童。所有患者均为早期前体B系急性淋巴细胞白血病,8名儿童有非标准风险的临床表现。使用一系列染色体显带技术证实了双着丝粒染色体的起源。通过荧光原位杂交(FISH),使用9号和20号染色体的涂染探针、着丝粒探针以及一些黏粒探针,进一步证实了这一结果。目前这些患者的随访时间过短,患者数量过少,尚无法确定这种染色体异常对预后的影响。

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