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首页> 外文期刊>Annals of diagnostic pathology >Angiomatoid fibrous histiocytoma: comparison of fluorescence in situ hybridization and reverse transcription polymerase chain reaction as adjunct diagnostic modalities
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Angiomatoid fibrous histiocytoma: comparison of fluorescence in situ hybridization and reverse transcription polymerase chain reaction as adjunct diagnostic modalities

机译:血管瘤样纤维组织细胞瘤:比较荧光原位杂交和逆转录聚合酶链反应作为辅助诊断方法

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摘要

Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue neoplasm of intermediate biologic potential and uncertain differentiation, most often arising in the extremities of children and young adults. Although it has characteristic histologic features of a lymphoid cuff surrounding nodules of ovoid cells with blood-filled cystic cavities, diagnosis is often difficult due to its morphologic heterogeneity and lack of specific immunoprofile. Angiomatoid fibrous histiocytoma is associated with recurrent chromosomal translocations, leading to characteristic EWSR1-CREB1, EWSR1-ATF1, and, rarely, FUS-ATF1 gene fusions; fluorescence in situ hybridization (FISH), detecting EWSR1 or PUS rearrangements, and reverse transcription-polymerase chain reaction (RT-PCR) for EWSR1-CREB1 and EWSR1-ATF1 fusion transcripts have become routine ancillary tools. We present a large comparative series of FISH and RT-PCR for AFH. Seventeen neoplasms (from 16 patients) histologically diagnosed as AFH were assessed for EWSR1 rearrangements or EWSR1-CREB1 and EWSR1-ATF1 fusion transcripts. All 17 were positive for either FISH or RT-PCR or both. Of 16, 14 (87.5%) had detectable EWSR1-CREB1 or EWSR1-ATF1 fusion transcripts by RT-PCR, whereas 13 (76.5%) of 17 had positive EWSR1 rearrangement with FISH. All 13 of 13 non-AFH control neoplasms failed to show EWSR1-CREB1 or EWSR1-ATF1 fusion transcripts, whereas EWSR1 rearrangement was present in 2 of these 13 cases (which were histopathologically myoepithelial neoplasms). This study shows that EWSR1-CREB1 or EWSR1-ATF1 fusions predominate in AFH (supporting previous reports that PUS rearrangement is rare in AFH) and that RT-PCR has a comparable detection rate to FISH for AFH. Importantly, cases of AFH can be missed if RTPCR is not performed in conjunction with FISH, and RT-PCR has the added advantage of specificity, which is crucial, as EWSR1 rearrangements are present in a variety of neoplasms in the histologic differential diagnosis of AFH, that differ in behavior and treatment (C) 2015 Elsevier Inc. All rights reserved.
机译:血管瘤样纤维组织细胞瘤(AFH)是一种罕见的软组织肿瘤,具有中等生物潜力和不确定的分化,最常见于儿童和年轻人的四肢。尽管它具有卵圆形细胞结节周围充满淋巴囊肿的淋巴囊的特征性组织学特征,但由于其形态上的异质性和缺乏特异性的免疫谱,通常难以诊断。血管瘤样纤维组织细胞瘤与复发性染色体易位有关,导致特征性的EWSR1-CREB1,EWSR1-ATF1,以及很少的FUS-ATF1基因融合。荧光原位杂交(FISH),检测EWSR1或PUS重排以及EWSR1-CREB1和EWSR1-ATF1融合转录本的逆转录聚合酶链反应(RT-PCR)已成为常规的辅助工具。我们提出了针对AFH的FISH和RT-PCR的大型比较系列。组织学诊断为AFH的17例肿瘤(来自16例患者)评估了EWSR1重排或EWSR1-CREB1和EWSR1-ATF1融合转录本。 FISH或RT-PCR或两者均阳性。在16个中,有14个(87.5%)通过RT-PCR检测到了EWSR1-CREB1或EWSR1-ATF1融合转录本,而17个中的13个(76.5%)在FISH的作用下EWSR1重排呈阳性。 13例非AFH对照肿瘤中的所有13例均未显示EWSR1-CREB1或EWSR1-ATF1融合转录本,而这13例病例中有2例发生了EWSR1重排(从组织病理学上来说是肌上皮肿瘤)。这项研究表明EWSR1-CREB1或EWSR1-ATF1融合在AFH中​​占主导地位(支持以前的报道,在AFH中​​PUS重排很少见),并且RT-PCR的AFH检测率与FISH相当。重要的是,如果不将RTPCR与FISH结合使用,则可能会漏诊AFH,而RT-PCR具有特异性的额外优势,这一点至关重要,因为EWSR1重排存在于AFH的组织学鉴别诊断中的多种肿瘤中,在行为和待遇上有所不同(C)2015 Elsevier Inc.保留所有权利。

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