arXiv:2511.05170cs.CV2025-11AAAI被引 2

MUSE通过自蒸馏提升病理切片中细胞核检测与分类性能。

MUSE: Multi-Scale Dense Self-Distillation for Nucleus Detection and Classification

  • 基于预测核位置的局部自蒸馏,实现跨尺度特征对齐。
  • 在三个基准上超越监督基线和通用病理模型。
  • 适合需要少标注数据的病理图像分析研究者。

组织病理学分析中的细胞核检测与分类(NDC)是支持多种高级病理应用的基础任务。然而,现有方法严重依赖耗时的细胞核级标注,且难以充分利用大规模未标注数据来学习判别性细胞核表示。本文提出MUSE(多尺度密集自蒸馏),一种专为NDC设计的新颖自监督学习方法。核心是NuLo(基于细胞核的局部自蒸馏),一种基于预测细胞核位置的坐标引导机制,可在不强制视图间严格空间对齐的情况下实现灵活的局部自蒸馏,从而解锁模型在细粒度细胞核级表征上的潜力。为支持MUSE,我们设计了一种简单有效的编码器-解码器架构及大视野半监督微调策略,最大化未标注病理图像的价值。在三个常用基准上的大量实验表明,MUSE有效解决了组织病理学NDC的核心挑战。所获模型不仅超越当前最先进的监督基线,还优于通用病理基础模型。

原文摘要 · Abstract (English)

Nucleus detection and classification (NDC) in histopathology analysis is a fundamental task that underpins a wide range of high-level pathology applications. However, existing methods heavily rely on labor-intensive nucleus-level annotations and struggle to fully exploit large-scale unlabeled data for learning discriminative nucleus representations. In this work, we propose MUSE (MUlti-scale denSE self-distillation), a novel self-supervised learning method tailored for NDC. At its core is NuLo (Nucleus-based Local self-distillation), a coordinate-guided mechanism that enables flexible local self-distillation based on predicted nucleus positions. By removing the need for strict spatial alignment between augmented views, NuLo allows critical cross-scale alignment, thus unlocking the capacity of models for fine-grained nucleus-level representation. To support MUSE, we design a simple yet effective encoder-decoder architecture and a large field-of-view semi-supervised fine-tuning strategy that together maximize the value of unlabeled pathology images. Extensive experiments on three widely used benchmarks demonstrate that MUSE effectively addresses the core challenges of histopathological NDC. The resulting models not only surpass state-of-the-art supervised baselines but also outperform generic pathology foundation models.

细胞核检测自监督学习病理分析

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