首页> 外文期刊>Cytogenetic and genome research >Novel Variant Ph Translocation t(9;22;11)(q34;q11.2;p15)inv(9)(p13q34) in Chronic Myeloid Leukemia Involving a One-Step Mechanism
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Novel Variant Ph Translocation t(9;22;11)(q34;q11.2;p15)inv(9)(p13q34) in Chronic Myeloid Leukemia Involving a One-Step Mechanism

机译:涉及一步机制的慢性粒细胞白血病中新型变体Ph易位t(9; 22; 11)(q34; q11.2; p15)inv(9)(p13q34)

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Chronic myeloid leukemia (CML) is a clonal malignant disorder of a pluripotent hematopoietic stem cell characterized by the presence of a Philadelphia (Ph) chromosome. Less than 10% of patients present variant Ph chromosomes involving 1 or more additional chromosomes, other than chromosomes 9 and 22, with uncertain prognosis. There are mainly 1- or 2-step mechanisms proposed to explain the genesis of variant Ph chromosomes depending on whether the involved chromosomes are simultaneously broken and rejoined or if a standard t(9;22) occurs first. By combined standard cytogenetic and FISH analysis we detected a novel variant Ph translocation among chromosomes 9, 11 and 22 in a patient with CML without progression to an accelerated phase of the disease after 7 years, with the derivative chromosome 9 also having an acquired pericentric inversion. This novel case illustrates the use of FISH in metaphase to confirm a new rearrangement not previously described in variant Ph formation and that the present karyotype could have originated by a 1-step mechanism with 4 simultaneous breakages without deletion of ABL1. Copyright (C) 2011 S. Karger AG, Basel
机译:慢性粒细胞白血病(CML)是多能造血干细胞的克隆性恶性疾病,其特征是存在费城(Ph)染色体。不到10%的患者呈现Ph变体染色体,其中涉及9条和22号染色体以外的1条或更多条附加染色体,预后不确定。提出主要有1步或2步机制来解释变体Ph染色体的发生,具体取决于所涉及的染色体是否同时断裂和重新结合,或者是否首先出现标准的t(9; 22)。通过标准的细胞遗传学和FISH分析,我们检测到7岁后CML患者在染色体9、11和22之间出现了新的变体Ph易位,并且在7年后没有进展为疾病的加速阶段,而衍生染色体9也具有后天性中心点倒置。这个新颖的案例说明了在中期使用FISH来确认以前在变体Ph形成中未描述的新重排,并且当前的核型可能由具有4个同时断裂的1步机制起源,而没有删除ABL1。版权所有(C)2011 S.Karger AG,巴塞尔

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