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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。

A novel three-way Philadelphia Variant t(9;22;17)(q34;q11.2;q12) in chronic myeloid leukemia: A case report.

作者信息

Allen-Proctor Kathy, Ruckdeschel Elizabeth, Naous Rana

机构信息

Department of Pathology, State University of New York-Upstate Medical University, Syracuse, NY 13210, USA.

出版信息

Mol Clin Oncol. 2018 Feb;8(2):300-301. doi: 10.3892/mco.2017.1529. Epub 2017 Dec 8.

Abstract

Chronic myeloid leukemia (CML) is a hematologic malignancy associated with increased circulating myeloid cells and platelets in the peripheral blood, with accompanying bone marrow hyperplasia. The Philadelphia chromosome, t(9;22)(q34;q11), is present in 95% of CML patients, resulting in constitutive tyrosine kinase activity; however, ~5% of CML patients possess a Philadelphia variant. A novel three-way Philadelphia translocation variant, t(9;22;17)(q34;q11.2;q11.2), was identified in a 54-year old man who presented with leukocytosis, anemia and thrombocytosis that was diagnosed with chronic myeloid leukemia, chronic phase. Cytogenetic analysis by G-banding revealed the presence of a three-way translocation involving the long arms of chromosomes 9, 22 and 17. Fluorescence hybridization utilizing a dual-color fusion probe confirmed the presence of the Bcr-Abl fusion gene.

摘要

慢性髓系白血病(CML)是一种血液系统恶性肿瘤,其外周血中循环髓系细胞和血小板增多,并伴有骨髓增生。95%的CML患者存在费城染色体,即t(9;22)(q34;q11),导致组成型酪氨酸激酶活性;然而,约5%的CML患者存在费城变异体。在一名54岁的男性患者中发现了一种新的三联费城易位变异体,即t(9;22;17)(q34;q11.2;q11.2),该患者表现为白细胞增多、贫血和血小板增多,被诊断为慢性髓系白血病慢性期。通过G显带进行的细胞遗传学分析显示存在涉及9号、22号和17号染色体长臂的三联易位。利用双色融合探针进行的荧光杂交证实了Bcr-Abl融合基因的存在。

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