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A rare chronic myeloid leukemia case with Philadelphia chromosome BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes

机译:罕见的慢性粒细胞白血病病例有费城染色体BCR-ABL e13a3转录本和涉及四个不同染色体的复杂易位

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摘要

The so-called Philadelphia (Ph) chromosome is present in more than 90% of chronic myeloid leukemia (CML) patients. Around 5–10% of these patients show complex translocations involving other chromosomes in addition to and/or besides chromosomes 9 and 22. CML cases with fusion transcripts, such as e13a3, in which ABL exon 3 rather than exon 2 has fused to BCR, are extremely rare. Such reported cases with the e13a3 transcript showed the Ph chromosome on karyotype analysis. This study reported a rare Ph chromosome-positive CML case with new complex chromosomal aberrations and an e13a3 BCR-ABL transcript that has yet to be established. A four-chromosome translocation involving chromosomal regions 12p11.2, 19q13.3, 9q34.1 and 22q11.2, besides a trisomy 8 and a derivative chromosome 12, were identified using high resolution multicolor banding. Reverse transcription polymerase chain reaction products showed the presence of BCR-ABL fusion transcript e13a3, and this signifies the major BCR breakpoint. The significance of the observed rearrangements and their possible role in the progression of CML was investigated.
机译:90%以上的慢性粒细胞白血病(CML)患者中都存在所谓的费城(Ph)染色体。这些患者中约有5–10%的患者表现出复杂的易位,涉及9号和22号染色体之外和/或之外的其他染色体。CML病例中有融合转录本,例如e13a3,其中ABL外显子3而非外显子2与BCR融合,非常稀有此类报道的带有e13a3转录本的病例在染色体核型分析中显示了Ph染色体。这项研究报告了罕见的Ph染色体阳性CML病例,具有新的复杂染色体畸变和e13a3 BCR-ABL转录本尚未建立。使用高分辨率多色条带,鉴定了涉及染色体区域12p11.2、19q13.3、9q34.1和22q11.2的四染色体易位,除了三体性8和衍生染色体12。逆转录聚合酶链反应产物显示BCR-ABL融合转录本e13a3的存在,这标志着主要的BCR断裂点。研究了观察到的重排的重要性及其在CML进展中的可能作用。

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