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在转化期具有e19a2转录本的伊马替尼治疗的慢性髓性白血病中,伴有双Ph的克隆进化随后出现四倍体。

Clonal evolution with double Ph followed by tetraploidy in imatinib-treated chronic myeloid leukemia with e19a2 transcript in transformation.

作者信息

Oshikawa Gaku, Kurosu Tetsuya, Arai Ayako, Murakami Naomi, Miura Osamu

机构信息

Department of Hematology, Tokyo Medical and Dental University, Bunkyoku, Japan.

出版信息

Cancer Genet Cytogenet. 2010 May;199(1):56-61. doi: 10.1016/j.cancergencyto.2010.01.018.

Abstract

Chronic myeloid leukemia (CML) with the e19a2 transcript coding for p230 is typically associated with a benign clinical course unless accompanied at presentation with additional chromosomal abnormalities. We report here a case of CML with e19a2 who did not show additional chromosomal abnormalities at diagnosis, but progressed to the fatal advanced stage in approximately 2 years. The patient was initially treated with imatinib, which, however, could be administered only intermittently at reduced doses because of recurrent thrombocytopenia and fluid retention. Nine months after starting imatinib, fluorescence in situ hybridization (FISH) with the BCR/ABL-ES fusion probe revealed 96% and 3% of bone marrow cells with one and two BCR/ABL1 fusion signals, respectively. Two years after starting therapy, leukocytosis recurred and the bone marrow contained 8.2% large and bizarre myeloblasts. Cytogenetic analysis revealed double Ph clones as well as tetraploid cells with four to five Ph chromosomes. FISH analysis confirmed the presence of cells with two to five BCR/ABL1 fusion signals. The patient died of disease progression in 2 months. No point mutation was detected in the region coding for the BCR/ABL tyrosine kinase domain by sequence analysis. It is speculated that the amplification of the BCR/ABL1 fusion gene by duplication of Ph and tetraploidy led to the progression of CML with the e19a2 transcript.

摘要

编码p230的e19a2转录本的慢性髓性白血病(CML)通常与良性临床病程相关,除非在初诊时伴有其他染色体异常。我们在此报告一例e19a2阳性的CML患者,其诊断时未显示其他染色体异常,但在约2年后进展至致命的晚期。患者最初接受伊马替尼治疗,然而,由于反复出现血小板减少和液体潴留,只能以减少的剂量间歇给药。开始伊马替尼治疗9个月后,使用BCR/ABL-ES融合探针进行荧光原位杂交(FISH)显示,分别有96%和3%的骨髓细胞具有一个和两个BCR/ABL1融合信号。开始治疗2年后,白细胞增多复发,骨髓中含有8.2%的大而怪异的原始粒细胞。细胞遗传学分析显示双Ph克隆以及具有四到五条Ph染色体的四倍体细胞。FISH分析证实存在具有两到五个BCR/ABL1融合信号的细胞。患者在2个月后死于疾病进展。通过序列分析在BCR/ABL酪氨酸激酶结构域的编码区域未检测到点突变。推测Ph重复和四倍体导致的BCR/ABL1融合基因扩增导致了e19a2转录本的CML进展。

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