Limei Guo

Peixiang Huang, Songtao Zhang, Yulu Gan et al. · pku

Deep learning in digital pathology brings intelligence and automation as substantial enhancements to pathological analysis, the gold standard of clinical diagnosis. However, multiple steps from tissue preparation to slide imaging introduce various image corruptions, making it difficult for deep neural network (DNN) models to achieve stable diagnostic results for clinical use. In order to assess and further enhance the robustness of the models, we analyze the physical causes of the full-stack corruptions throughout the pathological life-cycle and propose an Omni-Corruption Emulation (OmniCE) method to reproduce 21 types of corruptions quantified with 5-level severity. We then construct three OmniCE-corrupted benchmark datasets at both patch level and slide level and assess the robustness of popular DNNs in classification and segmentation tasks. Further, we explore to use the OmniCE-corrupted datasets as augmentation data for training and experiments to verify that the generalization ability of the models has been significantly enhanced.

Zhu Meng, Junhao Dong, Limei Guo et al.

Signet ring cells (SRCs), associated with a high propensity for peripheral metastasis and poor prognosis, critically influence surgical decision-making and outcome prediction. However, their detection remains challenging even for experienced pathologists. While artificial intelligence (AI)-based automated SRC diagnosis has gained increasing attention for its potential to enhance diagnostic efficiency and accuracy, existing methodologies lack systematic review. This gap impedes the assessment of disparities between algorithmic capabilities and clinical applicability. This paper presents a comprehensive survey of AI-driven SRC analysis from 2008 through June 2025. We systematically summarize the biological characteristics of SRCs and challenges in their automated identification. Representative algorithms are analyzed and categorized as unimodal or multi-modal approaches. Unimodal algorithms, encompassing image, omics, and text data, are reviewed; image-based ones are further subdivided into classification, detection, segmentation, and foundation model tasks. Multi-modal algorithms integrate two or more data modalities (images, omics, and text). Finally, by evaluating current methodological performance against clinical assistance requirements, we discuss unresolved challenges and future research directions in SRC analysis. This survey aims to assist researchers, particularly those without medical backgrounds, in understanding the landscape of SRC analysis and the prospects for intelligent diagnosis, thereby accelerating the translation of computational algorithms into clinical practice.

Binyu Zhang, Shichao Li, Junpeng Jian et al.

Prognostic task is of great importance as it closely related to the survival analysis of patients, the optimization of treatment plans and the allocation of resources. The existing prognostic models have shown promising results on specific datasets, but there are limitations in two aspects. On the one hand, they merely explore certain types of modal data, such as patient histopathology WSI and gene expression analysis. On the other hand, they adopt the per-cancer-per-model paradigm, which means the trained models can only predict the prognostic effect of a single type of cancer, resulting in weak generalization ability. In this paper, a deep-learning based model, named UMPSNet, is proposed. Specifically, to comprehensively understand the condition of patients, in addition to constructing encoders for histopathology images and genomic expression profiles respectively, UMPSNet further integrates four types of important meta data (demographic information, cancer type information, treatment protocols, and diagnosis results) into text templates, and then introduces a text encoder to extract textual features. In addition, the optimal transport OT-based attention mechanism is utilized to align and fuse features of different modalities. Furthermore, a guided soft mixture of experts (GMoE) mechanism is introduced to effectively address the issue of distribution differences among multiple cancer datasets. By incorporating the multi-modality of patient data and joint training, UMPSNet outperforms all SOTA approaches, and moreover, it demonstrates the effectiveness and generalization ability of the proposed learning paradigm of a single model for multiple cancer types. The code of UMPSNet is available at https://github.com/binging512/UMPSNet.

Xiaoyu Zheng, Jing Wen, Jiaxin Zhuang et al.

Polarization, as a new optical imaging tool, has been explored to assist in the diagnosis of pathology. Moreover, converting the polarimetric Mueller Matrix (MM) to standardized stained images becomes a promising approach to help pathologists interpret the results. However, existing methods for polarization-based virtual staining are still in the early stage, and the diffusion-based model, which has shown great potential in enhancing the fidelity of the generated images, has not been studied yet. In this paper, a Regulated Bridge Diffusion Model (RBDM) for polarization-based virtual staining is proposed. RBDM utilizes the bidirectional bridge diffusion process to learn the mapping from polarization images to other modalities such as H\&E and fluorescence. And to demonstrate the effectiveness of our model, we conduct the experiment on our manually collected dataset, which consists of 18,000 paired polarization, fluorescence and H\&E images, due to the unavailability of the public dataset. The experiment results show that our model greatly outperforms other benchmark methods. Our dataset and code will be released upon acceptance.

Yao Du, Jiaxin Zhuang, Xiaoyu Zheng et al.

Histopathology image analysis is fundamental to digital pathology, with hematoxylin and eosin (H&E) staining as the gold standard for diagnostic and prognostic assessments. While H&E imaging effectively highlights cellular and tissue structures, it lacks sensitivity to birefringence and tissue anisotropy, which are crucial for assessing collagen organization, fiber alignment, and microstructural alterations--key indicators of tumor progression, fibrosis, and other pathological conditions. To bridge this gap, we construct a polarization imaging system and curate a new dataset of over 13,000 paired Polar-H&E images. Visualizations of polarization properties reveal distinctive optical signatures in pathological tissues, underscoring its diagnostic value. Building on this dataset, we propose PolarHE, a dual-modality fusion framework that integrates H&E with polarization imaging, leveraging the latter ability to enhance tissue characterization. Our approach employs a feature decomposition strategy to disentangle common and modality specific features, ensuring effective multimodal representation learning. Through comprehensive validation, our approach significantly outperforms previous methods, achieving an accuracy of 86.70% on the Chaoyang dataset and 89.06% on the MHIST dataset. These results demonstrate that polarization imaging is a powerful and underutilized modality in computational pathology, enriching feature representation and improving diagnostic accuracy. PolarHE establishes a promising direction for multimodal learning, paving the way for more interpretable and generalizable pathology models.