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Topology-Guided Multi-Class Cell Context Generation for Digital Pathology.用于数字病理学的拓扑引导多类细胞上下文生成
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利用扩散模型生成组织病理学细胞拓扑结构

: Generating Histopathology Cell Topology with a Diffusion Model.

作者信息

Xu Meilong, Gupta Saumya, Hu Xiaoling, Li Chen, Abousamra Shahira, Samaras Dimitris, Prasanna Prateek, Chen Chao

机构信息

Stony Brook University, NY, USA.

Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, MA, USA.

出版信息

Proc IEEE Comput Soc Conf Comput Vis Pattern Recognit. 2025 Jun;2025:20979-20989. doi: 10.1109/cvpr52734.2025.01954. Epub 2025 Aug 13.

DOI:10.1109/cvpr52734.2025.01954
PMID:40873442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12380007/
Abstract

Accurately modeling multi-class cell topology is crucial in digital pathology, as it provides critical insights into tissue structure and pathology. The synthetic generation of cell topology enables realistic simulations of complex tissue environments, enhances downstream tasks by augmenting training data, aligns more closely with pathologists' domain knowledge, and offers new opportunities for controlling and generalizing the tumor microenvironment. In this paper, we propose a novel approach that integrates topological constraints into a diffusion model to improve the generation of realistic, contextually accurate cell topologies. Our method refines the simulation of cell distributions and interactions, increasing the precision and interpretability of results in downstream tasks such as cell detection and classification. To assess the topological fidelity of generated layouts, we introduce a new metric, Topological Fréchet Distance (TopoFD), which overcomes the limitations of traditional metrics like FID in evaluating topological structure. Experimental results demonstrate the effectiveness of our approach in generating multi-class cell layouts that capture intricate topological relationships. Code is available at https://github.com/Melon-Xu/TopoCellGen.

摘要

准确地对多类细胞拓扑结构进行建模在数字病理学中至关重要,因为它能为组织结构和病理学提供关键见解。细胞拓扑结构的合成生成能够对复杂的组织环境进行逼真模拟,通过扩充训练数据增强下游任务,更紧密地契合病理学家的领域知识,并为控制和概括肿瘤微环境提供新机会。在本文中,我们提出一种新颖的方法,将拓扑约束集成到扩散模型中,以改进逼真的、上下文准确的细胞拓扑结构的生成。我们的方法优化了细胞分布和相互作用的模拟,提高了细胞检测和分类等下游任务结果的精度和可解释性。为了评估生成布局的拓扑保真度,我们引入了一种新的度量标准,即拓扑弗雷歇距离(TopoFD),它克服了像FID这样的传统度量标准在评估拓扑结构方面的局限性。实验结果证明了我们的方法在生成捕捉复杂拓扑关系的多类细胞布局方面的有效性。代码可在https://github.com/Melon-Xu/TopoCellGen获取。