仅由t(10;12)(q24;p13)异常所致的难治性急性髓细胞白血病首例报道和文献回顾(英文)

来源 :北京大学学报(医学版) | 被引量 : 0次 | 上传用户:cuida3
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Rearrangements involving chromosome region at 12p13 are common abnormalities in hematological malignancies,including myeloid and lymphoid types. ETV6 gene is usually involved in the 12p13 region. ETV6 rearrangements are more often observed in acute lymphoblastic leukemia than in acute myeloid leukemia (AML),where ETV6 gene deletions are more common than rearrangements. Here,we report an AML case with the recurrent t(10;12)(q24;p13) as the sole abnormality. Fluore-scence in situ hybridization with mapping back to metaphases confirmed that the ETV6 gene splits,and rearranges with a locus at 10q24. In review of the literature,this is the first report of AML case with the novel abnormality as the sole change. Complete laboratory findings from bone marrow examination,flow cytometry analysis,cytogenetic studies,molecular analysis,and clinical features are also described in the report. Rearrangements involving chromosome regions at 12p13 are common abnormalities in hematological malignancies, including myeloid and lymphoid types. ETV6 gene is usually involved in the 12p13 region. ETV6 rearrangements are more often observed in acute lymphoblastic leukemia than in acute myeloid leukemia (AML), where ETV6 gene deletions are more common than rearrangements. Here, we report an AML case with the recurrent t (10; 12) (q24; p13) as the sole abnormality. Fluore-scence in situ hybridization with mapping back to metaphases confirmed that the the ETV6 gene splits, and rearranges with a locus at 10q24. In review of the literature, this is the first report of AML case with the novel abnormality as the sole change. Complete laboratory findings from bone marrow examination, flow cytometry analysis, cytogenetic studies, molecular analysis , and clinical features are also described in the report.
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