A Topological Comparison of the Fluorescence Imitating Brightfield Imaging and H&E Imaging.

Meiliong Xu, Nate Anderson, Richard M Levenson, Prateek Prasanna, Chao Chen
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Abstract

Fluorescence Imitating Brightfield Imaging (FIBI) represents an innovative approach in microscopy, providing real-time, non-destructive imaging of tissue without the need for the preparation of thin sections mounted on glass slides. The non-destructive nature of the technology permits tissue preservation for downstream analysis, which makes FIBI a promising alternative to traditional hematoxylin and eosin (H&E) staining in histopathology. Previous research has shown that FIBI can identify morphological features with similar or, in some cases, higher quality compared with H&E images. To comprehensively quantify the advantages and limitations of FIBI in tissue visualization, we propose a novel framework for characterizing the topological difference of FIBI and H&E slide pairs. Experiments are performed on slide pairs of FIBI and H&E imaging of the same tissue area. The proposed approach shows that FIBI can make morphological structures, like vessels, more salient and holds great promise as a complementary technique to H&E, offering novel insights into tissue architecture and potentially improving histopathological diagnostic accuracy.

荧光模拟明场成像与H&E成像的拓扑比较。
荧光模拟明场成像(FIBI)代表了显微镜中的一种创新方法,提供了实时的、非破坏性的组织成像,而不需要在玻璃载玻片上制备薄片。该技术的非破坏性特性允许组织保存用于下游分析,这使得FIBI在组织病理学上成为传统苏木精和伊红(H&E)染色的有希望的替代品。先前的研究表明,FIBI可以识别与H&E图像相似或在某些情况下质量更高的形态学特征。为了全面量化FIBI在组织可视化中的优势和局限性,我们提出了一个新的框架来表征FIBI和H&E玻片对的拓扑差异。实验对同一组织区域的FIBI和H&E成像进行玻片配对。所提出的方法表明,FIBI可以使血管等形态结构更加突出,并且作为H&E的补充技术具有很大的前景,为组织结构提供了新的见解,并有可能提高组织病理学诊断的准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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