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Congenital B-lymphoblastic leukemia with a cryptic MLL rearrangement and post-treatment evolution to mixed phenotype acute leukemia

机译:先天性B淋巴细胞白血病伴有MLL隐匿性重排和治疗后演变为混合表型急性白血病

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Congenital leukemia is a rare event with a poor prognosis. We report a case of congenital leukemia with a cryptic rearrangement of MLL demonstrable only with RT-PCR. Interestingly, with treatment, the patient showed lineage plasticity of the leukemia with the development of monocytic lineage blasts after presenting with B-cell lineage blasts. This was heralded by the development of a new clonal cytogenetic abnormality. This case highlights the primitive nature of the leukemic cells in congenital leukemia, and emphasizes that RT-PCR for MLL rearrangements may identify a subset of cases which are otherwise negative by karyotyping, FISH, and chromosomal microarrays.
机译:先天性白血病是罕见的预后不良事件。我们报告一例先天性白血病,MLL隐匿性重排仅在RT-PCR证实。有趣的是,在接受B细胞谱系胚细胞治疗后,患者随着单核细胞谱系胚细胞的发展,显示出白血病谱系可塑性。新的克隆细胞遗传学异常的发展预示着这一点。该病例突出了先天性白血病中白血病细胞的原始性质,并强调了用于MLL重排的RT-PCR可能会鉴定出一部分病例,这些病例否则会因核型,FISH和染色体微阵列检测为阴性。

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