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A New Chromosome Translocation t(7;16)(q31,q22) Change during an Acute Promyelocytic Leukemia Relapse

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单位: [1]Huazhong Univ Sci & Technol, Dept Hematol, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Peoples R China
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关键词: Acute promyelocytic leukemia Additional chromosomal abnormalities fms-related tyrosine kinase 3 Relapse t(7 16)(q31 q22)

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The translocation t(15;17), which results in the PML-RAR alpha fusion gene, is a characteristic chromosomal translocation in acute promyelocytic leukemia (APL). But additional chromosome aberrations in APL are increasingly recognized. Here, we report on a 16-year-old APL patient who had an fms-related tyrosine kinase 3-internal tandem duplication (FLT3-ITD) and a 46,XY,t(15;17)(q22;q21)-16+mar karyotype at diagnosis. The patient achieved complete remission after induction therapy with all-trans retinoic acid and chemotherapy. But he soon relapsed presenting distinctive APL features in the bone marrow and leptomeninges and showing a chromosome translocation change involving chromosomes 7 and 16 besides t(15;17)(q22;q21). The new karyotype 46, XY,t(7;16) (q31;q22),t(15;17)(q22;q21) was determined. To the best of our knowledge, this is the first report of a de novo APL with a chromosome translocation t(7; 16)(q31,q22) together with a t(15;17)(q22;q21) and FLT3-ITD mutation. Copyright (c) 2013 S. Karger AG, Basel

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出版当年[2012]版:
大类 | 4 区 生物
小类 | 4 区 细胞生物学 4 区 遗传学
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大类 | 4 区 生物学
小类 | 4 区 细胞生物学 4 区 遗传学
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出版当年[2011]版:
Q4 CELL BIOLOGY Q4 GENETICS & HEREDITY
最新[2023]版:
Q3 GENETICS & HEREDITY Q4 CELL BIOLOGY

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第一作者单位: [1]Huazhong Univ Sci & Technol, Dept Hematol, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Peoples R China
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