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一名慢性髓性白血病患者中BCR-ABL1融合序列的异常定位。

Unusual location of BCR-ABL1 fusion sequences in a chronic myeloid leukemia patient.

作者信息

Zámečníkova Adriana, Al Bahar Soad, Pandita Ramesh

机构信息

Department of Hematology, Kuwait Cancer Control Center, Shuwaikh, Kuwait.

出版信息

Hematology. 2012 Nov;17(6):321-4. doi: 10.1179/1607845412Y.0000000012. Epub 2012 Sep 14.

Abstract

We describe a case of a chronic myeloid leukemia patient displaying the chimeric BCR-ABL1 gene on 12p11. Chromosome analysis revealed complex chromosome aberration involving chromosomes 9, 12, and 22. Fluorescence in situ hybridization revealed an unusual signal pattern revealing the BCR-ABL1 fusion signal on chromosome 12, while no reciprocal ABL1-BCR fusion was detected on der(9) chromosome. The relocation of BCR-ABL1 fusion sequences to 12p11 site in our patient represents a rare type of variant translocation, as in almost all patients the chimeric BCR-ABL1 gene is located on der(22) chromosome. Our case illustrates the challenge of recognizing a complex pattern of cytogenetic aberrations that occur with variant t(9;22) and may add further information about clinical significance of unusual variant Ph rearrangements in CML patients receiving tyrosine kinase inhibitor treatment.

摘要

我们描述了一例慢性髓性白血病患者,其12p11上显示有嵌合的BCR-ABL1基因。染色体分析显示涉及9号、12号和22号染色体的复杂染色体畸变。荧光原位杂交显示出一种不寻常的信号模式,在12号染色体上显示出BCR-ABL1融合信号,而在der(9)染色体上未检测到相互的ABL1-BCR融合。在我们的患者中,BCR-ABL1融合序列重定位到12p11位点代表一种罕见的变异易位类型,因为几乎所有患者的嵌合BCR-ABL1基因都位于der(22)染色体上。我们的病例说明了识别变异t(9;22)时出现的复杂细胞遗传学畸变模式的挑战,并可能为接受酪氨酸激酶抑制剂治疗的慢性粒细胞白血病患者中不寻常的变异Ph重排的临床意义提供更多信息。

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