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Prototype-Based Image Prompting for Weakly Supervised Histopathological Image Segmentation

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arxiv 2503.12068 v1 pith:XN7PIULN submitted 2025-03-15 cs.CV

classification cs.CV
keywords imagesegmentationhistopathologicalsupervisedweaklyapproachescamsclass
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Weakly supervised image segmentation with image-level labels has drawn attention due to the high cost of pixel-level annotations. Traditional methods using Class Activation Maps (CAMs) often highlight only the most discriminative regions, leading to incomplete masks. Recent approaches that introduce textual information struggle with histopathological images due to inter-class homogeneity and intra-class heterogeneity. In this paper, we propose a prototype-based image prompting framework for histopathological image segmentation. It constructs an image bank from the training set using clustering, extracting multiple prototype features per class to capture intra-class heterogeneity. By designing a matching loss between input features and class-specific prototypes using contrastive learning, our method addresses inter-class homogeneity and guides the model to generate more accurate CAMs. Experiments on four datasets (LUAD-HistoSeg, BCSS-WSSS, GCSS, and BCSS) show that our method outperforms existing weakly supervised segmentation approaches, setting new benchmarks in histopathological image segmentation.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. ProBAG: Prototype-Guided Boundary-Aware Graph Diffusion for Weakly Supervised Histopathology Segmentation

    cs.CV 2026-08 conditional novelty 5.0 of 10

    ProBAG improves weakly supervised histopathology segmentation by blending CONCH text prototypes with visual prototypes and adding a boundary-aware graph diffusion step.

  2. Multimodal Cancer Survival Analysis via Hypergraph Learning with Cross-Modality Rebalance

    cs.CV 2025-05 conditional novelty 5.0 of 10

    MRePath uses sheaf hypergraphs on pathology patches plus dynamic weighting to fuse genomics, reaching a mean C-Index of 71.5%, about 3 points above prior multimodal baselines on five TCGA datasets.

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