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两名慢性粒细胞白血病患者中的一种复杂的三向易位(4;9;22)

A three way complex translocation (4; 9; 22) in two patients with chronic myelocytic leukemia.

作者信息

Sheth Frenny J, Sheth Jayesh J, Verhest Alain

机构信息

FRIGE (Foundation for Research in Genetics and Endocrinology) Genetic Centre, 20/1, Bima Nagar, Satellite, Ahmedabad-380 015, India.

出版信息

J Cancer Res Ther. 2005 Apr-Jun;1(2):108-10. doi: 10.4103/0973-1482.16711.

DOI:10.4103/0973-1482.16711
PMID:17998637
Abstract

Chronic myeloid leukemia (CML) is genetically characterized by the reciprocal translocation of chromosome 9 and 22, t(9;22)(q34;q11) which results in the fusion of BCR/ABL gene observed on the derivative chromosome 22 called Philadelphia (Ph') chromosome. About 5-8% of Philadelphia positive patients with CML show various complex translocations involving third chromosome in addition to chromosome 9 and 22. In present report we discuss two cases with CML referred at our centre. At the time of initial diagnosis and after 9 months of treatment, one of the patients showed 100% presence of Philadelphia positive in bone marrow culture. During follow-up in an accelerated state, his cytogenetic study revealed a complex translocation (4;9;22)(q25;q34;q11) along with an additional Philadelphia and marker chromosome. The second patient showed a complex (4;9;22)(q25;q34;q11) translocation at the time of diagnosis. He was on hydroxyurea and his follow-up cytogenetic study after the course of chemotherapy showed no changes. Further confirmation of complex translocation was done by FISH study using bcr/abl and whole chromosome 9 probes. Though the additional genes involved in complex variant Ph' rearrangements have not been characterized, both patients are healthy till 3 to 5 years of initial diagnosis. This could be attributed to the benign effect resulted from reciprocal translocation with no loss or gain of the genetic material.

摘要

慢性粒细胞白血病(CML)的遗传学特征是9号和22号染色体相互易位,即t(9;22)(q34;q11),这导致在衍生的22号染色体(称为费城染色体(Ph'染色体))上观察到BCR/ABL基因融合。约5-8%的费城染色体阳性CML患者除9号和22号染色体外,还表现出涉及第三条染色体的各种复杂易位。在本报告中,我们讨论了在我们中心转诊的2例CML患者。在初次诊断时以及治疗9个月后,其中1例患者骨髓培养中费城染色体阳性率为100%。在加速期随访期间,他的细胞遗传学研究显示存在复杂易位(4;9;22)(q25;q34;q11),同时还有一条额外的费城染色体和一条标记染色体。第2例患者在诊断时显示存在复杂的(4;9;22)(q25;q34;q11)易位。他接受羟基脲治疗,化疗疗程后的随访细胞遗传学研究显示无变化。使用bcr/abl和9号全染色体探针进行的荧光原位杂交(FISH)研究进一步证实了复杂易位。尽管参与复杂变异Ph'重排的其他基因尚未明确,但这2例患者自初次诊断起3至5年一直健康。这可能归因于相互易位产生的良性效应,没有遗传物质的丢失或增加。

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引用本文的文献

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A unique three-way Philadelphia chromosome variant t(4;9;22)(q21;q34;q11.2) in a newly diagnosed patient with chronic phase chronic myeloid leukemia: a case report and review of the literature.一例新诊断的慢性期慢性髓性白血病患者中独特的三向费城染色体变异t(4;9;22)(q21;q34;q11.2):病例报告及文献复习
J Med Case Rep. 2021 May 25;15(1):285. doi: 10.1186/s13256-021-02885-4.
2
A novel three-way Philadelphia Variant t(9;22;17)(q34;q11.2;q12) in chronic myeloid leukemia: A case report.慢性髓系白血病中的一种新型三向费城变异t(9;22;17)(q34;q11.2;q12):一例报告。
Mol Clin Oncol. 2018 Feb;8(2):300-301. doi: 10.3892/mco.2017.1529. Epub 2017 Dec 8.
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Genetic counseling in carriers of reciprocal translocations involving two autosomes.
涉及两条常染色体的相互易位携带者的遗传咨询
Indian J Hum Genet. 2012 May;18(2):250-3. doi: 10.4103/0971-6866.100802.