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Mature B-cell acute lymphoblastic leukemia with t(9;11) translocation: a distinct subset of B-cell acute lymphoblastic leukemia

机译:具有t(9; 11)易位的成熟B细胞急性淋巴细胞白血病:B细胞急性淋巴细胞白血病的不同子集

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Mature B-cell acute lymphoblastic leukemia (ALL) is typically associated with the FAB-L3 morphology and rearrangement of the MYC gene, features characteristic of the leukemic phase of Burkitt's lymphoma. However, the term 'mature' has also been used to describe other rare cases of B-ALL with light-chain surface immunoglobulin expression. In contrast, infantile B-cell ALL is generally characterized by rearrangement of the MLL gene, an immature pro-B-cell phenotype, and CD10 negativity. We describe two unusual cases of infantile B-ALL with non-L3 morphology, expressing a mature B-cell phenotype ( sIg+, CD19+, CD10-, TdT-, and CD34-), and showing MLL rearrangement without MYC rearrangement at presentation. Both infants relapsed after months of morphologic and genetic remission. At relapse, the t(9;11) translocation was detected in both cases by spectral karyotyping. After the initial relapse, both cases followed a rapid and aggressive course. Literature search identified few similar cases, all expressed surface immunoglobulin and showed MLL rearrangement (majority with the t(9;11) translocation). These cases show that B-ALL with MLL rearrangement, especially the t(9;11) translocation, can express a 'mature' B-cell phenotype and may represent a distinct subset. Identification of additional cases will further clarify the significance of MLL rearrangements in mature B-ALL.
机译:成熟的B细胞急性淋巴细胞白血病(ALL)通常与FAB-L3形态和MYC基因重排有关,这是伯基特淋巴瘤白血病期的特征。但是,术语“成熟”也已用于描述具有轻链表面免疫球蛋白表达的B-ALL的其他罕见情况。相反,婴儿B细胞ALL的特征通常在于MLL基因的重排,未成熟的B细胞前表型和CD10阴性。我们描述了两个非L3形态的婴儿B-ALL的罕见病例,它们表达了成熟的B细胞表型(sIg +,CD19 +,CD10-,TdT-和CD34-),并在展示时显示了无MYC重排的MLL重排。两个月的形态学和遗传学缓解后均复发。在复发时,通过光谱核型分析在两种情况下均检测到t(9; 11)易位。最初的复发后,两个病例均经历了快速而积极的过程。文献检索发现了一些相似的病例,都表达了表面免疫球蛋白,并显示了MLL重排(多数伴随t(9; 11)易位)。这些情况表明,具有MLL重排的B-ALL,特别是t(9; 11)易位,可以表达“成熟的” B细胞表型,并且可以代表不同的子集。鉴定其他病例将进一步阐明成熟B-ALL中MLL重排的重要性。

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