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Malignant solitary fibrous tumor with high-grade nuclear atypia: An alternate entity for the undetermined tumor group

机译:恶性孤立性纤维性肿瘤伴高度核不典型:未定肿瘤组的另一种实体

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Recently, a novel fusion transcript, NAB2-STAT6, and its variants have also been reported to be specific diagnostic markers for solitary fibrous tumors (SFTs). In this study, we validated the existence of the NAB2-STAT6 fusion gene in SETs and examined its relation with the pathological features. Frozen samples from 9 tumors were assessed for fusion gene. The detected fusion genes exhibited large intron sequences and the insertion of unknown and previously unreported sequences. The fusion genes were not detected in the 2 malignant cases with high-grade nuclear atypia, nuclear pleomorphism and necrosis, that was confirmed by multiplex PCR method. In addition, 1 of the 2 NAB2-STAT6 fusion gene-negative tumors showed amplification of the MDM2 and CDK4 genes. It was suggested that a certain proportion of tumors previously diagnosed as malignant SFTs with high-grade nuclear atypia lacking NAB2-STAT6 should be categorized into a special subtype of SFT, which is genetically different from conventional SFTs, and which cannot be apparently distinguished from dedifferentiated liposarcoma or undifferentiated pleomorphic sarcoma. (C) 2014 Elsevier GmbH. All rights reserved.
机译:最近,还报道了一种新型的融合转录本NAB2-STAT6及其变异体是孤立性纤维性肿瘤(SFT)的特异性诊断标记。在这项研究中,我们验证了SET中NAB2-STAT6融合基因的存在,并检查了其与病理特征的关系。评估了来自9个肿瘤的冷冻样品的融合基因。检测到的融合基因表现出大的内含子序列以及未知和先前未报道序列的插入。多重PCR方法证实了2例高级别核型异型,核多型性和坏死的恶性病例中未检测到融合基因。此外,在2个NAB2-STAT6融合基因阴性肿瘤中,有1个显示出MDM2和CDK4基因的扩增。建议将一定比例的先前被诊断为恶性SFT且缺乏NAB2-STAT6的高度核非典型性恶性肿瘤归为SFT的一种特殊亚型,该亚型在遗传上与常规SFT不同,并且不能与去分化进行明显区别脂肪肉瘤或未分化的多形性肉瘤。 (C)2014 Elsevier GmbH。版权所有。

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