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一名患有B细胞淋巴细胞白血病的儿科患者中的MLL基因重复。

MLL duplication in a pediatric patient with B-cell lymphoblastic lymphoma.

作者信息

Mater David Van, Goodman Barbara K, Wang Endi, Gaca Ana M, Wechsler Daniel S

机构信息

Department of Pediatrics, Duke University, Durham, NC, USA.

出版信息

J Pediatr Hematol Oncol. 2012 Apr;34(3):e120-3. doi: 10.1097/MPH.0b013e3182273b57.

Abstract

Lymphoblastic lymphoma is the second most common type of non-Hodgkin lymphoma seen in children. Approximately, 90% of lymphoblastic lymphomas arise from T cells, with the remaining 10% being B-cell-lineage derived. Although T-cell lymphoblastic lymphoma most frequently occurs in the anterior mediastinum (thymus), B-cell lymphoblastic lymphoma (B-LBL) predominates in extranodal sites such as skin and bone. Here, we describe a pediatric B-LBL patient who presented with extensive abdominal involvement and whose lymphoma cells displayed segmental duplication of the mixed lineage leukemia (MLL) gene. MLL duplication/amplification has been described primarily in acute myeloid leukemia and myelodysplastic syndrome with no published reports of discrete MLL duplication/amplification events in B-LBL. The MLL gene duplication noted in this case may represent a novel mechanism for tumorigenesis in B-LBL.

摘要

淋巴母细胞淋巴瘤是儿童中第二常见的非霍奇金淋巴瘤类型。大约90%的淋巴母细胞淋巴瘤起源于T细胞,其余10%来源于B细胞系。尽管T细胞淋巴母细胞淋巴瘤最常发生在前纵隔(胸腺),但B细胞淋巴母细胞淋巴瘤(B-LBL)在皮肤和骨骼等结外部位更为常见。在此,我们描述了一名患有广泛腹部受累的儿童B-LBL患者,其淋巴瘤细胞显示混合谱系白血病(MLL)基因的节段性重复。MLL重复/扩增主要在急性髓系白血病和骨髓增生异常综合征中被描述,尚无关于B-LBL中离散MLL重复/扩增事件的报道。该病例中发现的MLL基因重复可能代表了B-LBL肿瘤发生的一种新机制。

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