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首页> 外文期刊>Leukemia >Variant t(2;11)(p11;q13) associated with the IgK-CCND1 rearrangement is a recurrent translocation in leukemic small-cell B-non-Hodgkin lymphoma
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Variant t(2;11)(p11;q13) associated with the IgK-CCND1 rearrangement is a recurrent translocation in leukemic small-cell B-non-Hodgkin lymphoma

机译:与IgK-CCND1重排相关的变体t(2; 11)(p11; q13)是白血病小细胞B型非霍奇金淋巴瘤的反复易位

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Classical t(11;14)(q13;q32) involving IGH-CCND1 is typically associated with aggressive CD5-positive mantle cell lymphoma (MCL). Recently, we identified the IGK variant of this translocation, t(2;11)(p11;q13), in three patients with a leukemic small-cell B-non-Hodgkin lymphoma. In all cases, rearrangements of the IGK and CCND1 genes were demonstrated by fluorescence in situ hybridization. Moreover, we mapped the 11q13 breakpoint of this variant translocation in the 3' region of CCND1 which contrasts with the 5' breakpoints in a standard t(11;14)(q13;q32). Expression of cyclin D1 was shown in two cases analyzed either at diagnosis or during disease progression. All three patients were asymptomatic at presentation and no initial therapy was required. One patient died of a progressive disease 58 months from diagnosis, and two patients showed stable disease after 12 months of follow-up. In two analyzed cases, mutated IGVH genes were identified. Our findings indicate that variant t(2;11)(p11;q13) does not typify a classical MCL but possibly a more indolent leukemic lymphoma originating from an antigen experienced (mutated) B cell.
机译:涉及IGH-CCND1的经典t(11; 14)(q13; q32)通常与侵袭性CD5阳性套细胞淋巴瘤(MCL)相关。最近,我们在三名患有白血病小细胞B型非霍奇金淋巴瘤的患者中鉴定了这种易位的IGK变体t(2; 11)(p11; q13)。在所有情况下,IGK和CCND1基因的重排均通过荧光原位杂交得到证明。此外,我们在CCND1的3'区域中映射了此变体易位的11q13断点,这与标准t(11; 14)(q13; q32)中的5'断点形成了对比。在诊断或疾病进展期间分析的两个病例中显示了细胞周期蛋白D1的表达。所有三位患者在就诊时均无症状,不需要初始治疗。一名患者在确诊后58个月内死于进行性疾病,而两名患者在随访12个月后表现出稳定的疾病。在两个分析的案例中,鉴定出突变的IGVH基因。我们的发现表明,变体t(2; 11)(p11; q13)不能代表典型的MCL,而可能代表源自抗原经历(突变)的B细胞的更温和的白血病淋巴瘤。

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