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首页> 外文期刊>Human Pathology >Anaplastic lymphoma kinase-positive large B-cell lymphoma with complex karyotype and novel ALK gene rearrangements.
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Anaplastic lymphoma kinase-positive large B-cell lymphoma with complex karyotype and novel ALK gene rearrangements.

机译:间变性淋巴瘤激酶阳性的大B细胞淋巴瘤,具有复杂的核型和新的ALK基因重排。

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摘要

Anaplastic lymphoma kinase-positive large B-cell lymphoma is a rare non-Hodgkin lymphoma that exhibits a characteristic immunoblastic/plasmablastic morphology and is frequently associated with t(2;17)(p23;q23) and expression of Clathrin-anaplastic lymphoma kinase fusion protein. Here, we report a refractory anaplastic lymphoma kinase-positive large B-cell lymphoma in a 49-year-old human immunodeficiency virus-positive man. The neoplastic cells expressed CD138, epithelial membrane antigen, CD45, and perforin, and showed a strong granular cytoplasmic anaplastic lymphoma kinase staining pattern. Conventional chromosome analysis revealed a clone with multiple anomalies and a chromosome count of 76 to 79. Fluorescence in situ hybridization studies showed 5 copies of the ALK gene with 2 intact signals and 3 signals resulting from 2 independent, previously unreported, rearrangements. One rearrangement, seen in 2 copies, involved translocation of ALK sequences to chromosome Xq21. The second rearrangement involved translocation of ALK sequences to chromosome 12q24.1. This case broadens the cytogenetic alterations in anaplastic lymphoma kinase-positive large B-cell lymphoma, and it also demonstrates the high genetic instability of this tumor.
机译:间变性淋巴瘤激酶阳性的大B细胞淋巴瘤是一种罕见的非霍奇金淋巴瘤,表现出特征性的免疫母细胞/浆母细胞形态,经常与t(2; 17)(p23; q23)和网格蛋白-间变性淋巴瘤激酶融合蛋白的表达相关蛋白。在这里,我们报告了一个49岁的人类免疫缺陷病毒阳性男子的难治性间变性淋巴瘤激酶阳性大B细胞淋巴瘤。赘生性细胞表达CD138,上皮膜抗原,CD45和穿孔素,并显示强颗粒状的细胞质间变性淋巴瘤激酶染色模式。传统的染色体分析显示出一个克隆,该克隆具有多个异常且染色体数为76至79。荧光原位杂交研究显示5个拷贝的ALK基因具有2个完整信号和3个信号,这些信号来自2个独立的,以前未报告的重排。一式两份的重排涉及将ALK序列转位至Xq21染色体。第二次重排涉及将ALK序列易位至染色体12q24.1。该病例扩大了间变性淋巴瘤激酶阳性大B细胞淋巴瘤的细胞遗传学改变,也证明了这种肿瘤的高度遗传不稳定性。

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