Xu Meiliong, Anderson Nate, Levenson Richard M, Prasanna Prateek, Chen Chao
Department of Computer Science, Stony Brook University, New York, USA.
Department of Pathology and Laboratory Medicine, University of California, Davis, USA.
Int Workshop Topol Graph Inf Imaging Inform (2024). 2025;15239:122-133. doi: 10.1007/978-3-031-73967-5_12. Epub 2024 Oct 11.
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(FIBI)是显微镜技术中的一种创新方法,可对组织进行实时、无损成像,无需制备安装在载玻片上的薄切片。该技术的无损特性允许保留组织用于下游分析,这使得FIBI在组织病理学中成为传统苏木精和伊红(H&E)染色的一个有前景的替代方法。先前的研究表明,与H&E图像相比,FIBI能够识别出相似的形态特征,在某些情况下质量更高。为了全面量化FIBI在组织可视化中的优势和局限性,我们提出了一个用于表征FIBI和H&E玻片对拓扑差异的新框架。对同一组织区域的FIBI和H&E成像的玻片对进行了实验。所提出的方法表明,FIBI可以使血管等形态结构更加突出,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。