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首页> 外文期刊>Human Pathology >Whole-slide imaging is a robust alternative to traditional fluorescent microscopy for fluorescence in situ hybridization imaging using break-apart DNA probes
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Whole-slide imaging is a robust alternative to traditional fluorescent microscopy for fluorescence in situ hybridization imaging using break-apart DNA probes

机译:全幻灯片成像是使用断裂DNA探针进行荧光原位杂交成像的传统荧光显微镜的强大替代品

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Fluorescence in situ hybridization is an indispensable technique used in routine pathology and for theranostic purposes. Because fluorescence in situ hybridization techniques require sophisticated microscopic workstations and long procedures of image acquisition with sometimes subjective and poorly reproducible results, we decided to test a whole-slide imaging system as an alternative approach. In this study, we used the latest generation of Pannoramic 250 Flash digital microscopes (P250 Flash digital microscopes; 3DHISTECH, Budapest, Hungary) to digitize fluorescence in situ hybridization slides of diffuse large B cells lymphoma cases for detecting MYC rearrangement. The P250 Flash digital microscope was found to be precise with better definition of split signals in cells containing MYC rearrangement with fewer truncated signals as compared to traditional fluorescence microscopy. This digital technique is easier thanks to the preview function, which allows almost immediate identification of the tumor area, and the panning and zooming functionalities as well as a shorter acquisition time. Moreover, fluorescence in situ hybridization analyses using the digital technique appeared to be more reproducible between pathologists. Finally, the digital technique also allowed prolonged conservation of photos. In conclusion, whole-slide imaging technologies represent rapid, robust, and highly sensitive methods for interpreting fluorescence in situ hybridization slides with break-apart probes. In addition, these techniques offer an easier way to interpret the signals and allow definitive storage of the images for pathology expert networks or e-learning databases.
机译:荧光原位杂交是常规病理学和治疗学目的不可或缺的技术。由于荧光原位杂交技术需要复杂的显微工作站和较长的图像采集程序,有时会产生主观的且可再现性差的结果,因此我们决定测试全幻灯片成像系统作为替代方法。在这项研究中,我们使用了最新一代的Pannoramic 250 Flash数码显微镜(P250 Flash数码显微镜; 3DHISTECH,匈牙利布达佩斯)将数字化的弥漫大B细胞淋巴瘤病例的荧光原位杂交玻片数字化,以检测MYC重排。发现P250 Flash数字显微镜非常精确,与传统的荧光显微镜相比,在含有MYC重排的细胞中分裂信号的定义更好,截短的信号更少。借助预览功能,该数字技术更加容易,它可以几乎立即识别出肿瘤区域,平移和缩放功能以及更短的采集时间。此外,病理学家之间使用数字技术进行的荧光原位杂交分析似乎更具可重复性。最后,数字技术还可以长时间保存照片。总之,全玻片成像技术代表了一种快速,可靠,高度灵敏的方法,用于解释带有断裂探针的荧光原位杂交玻片。此外,这些技术为病理学专家网络或电子学习数据库提供了一种更简便的方法来解释信号并允许对图像进行明确的存储。

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