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arXiv 提交日期: 2026-02-03
📄 Abstract - Quasi-multimodal-based pathophysiological feature learning for retinal disease diagnosis

Retinal diseases spanning a broad spectrum can be effectively identified and diagnosed using complementary signals from multimodal data. However, multimodal diagnosis in ophthalmic practice is typically challenged in terms of data heterogeneity, potential invasiveness, registration complexity, and so on. As such, a unified framework that integrates multimodal data synthesis and fusion is proposed for retinal disease classification and grading. Specifically, the synthesized multimodal data incorporates fundus fluorescein angiography (FFA), multispectral imaging (MSI), and saliency maps that emphasize latent lesions as well as optic disc/cup regions. Parallel models are independently trained to learn modality-specific representations that capture cross-pathophysiological signatures. These features are then adaptively calibrated within and across modalities to perform information pruning and flexible integration according to downstream tasks. The proposed learning system is thoroughly interpreted through visualizations in both image and feature spaces. Extensive experiments on two public datasets demonstrated the superiority of our approach over state-of-the-art ones in the tasks of multi-label classification (F1-score: 0.683, AUC: 0.953) and diabetic retinopathy grading (Accuracy:0.842, Kappa: 0.861). This work not only enhances the accuracy and efficiency of retinal disease screening but also offers a scalable framework for data augmentation across various medical imaging modalities.

顶级标签: medical multi-modal computer vision
详细标签: retinal disease diagnosis multimodal fusion medical image synthesis feature learning pathophysiological signatures 或 搜索:

基于准多模态的视网膜疾病诊断病理特征学习方法 / Quasi-multimodal-based pathophysiological feature learning for retinal disease diagnosis


1️⃣ 一句话总结

这篇论文提出了一种创新的‘准多模态’学习框架,通过合成并融合多种眼部影像数据来自动学习疾病特征,有效解决了实际医疗中多模态数据难以获取和匹配的难题,从而显著提升了视网膜疾病(如糖尿病视网膜病变)自动分类与分级的准确性和效率。

源自 arXiv: 2602.03622