用弱监督方法提升SAM在肠息肉和皮肤癌分割中的精度
BiSeg-SAM: Weakly-Supervised Post-Processing Framework for Boosting Binary Segmentation in Segment Anything Models
- 用弱标签引导SAM,通过框提示和多选掩码转框增强定位
- 在5个肠息肉和1个皮肤癌数据集上超越现有最佳方法
- 仅需少量真实标签即可精修边界,适合标注成本高的医疗场景
准确分割肠息肉和皮肤病变对结直肠癌和皮肤癌诊断至关重要。尽管已有多种基于全监督深度学习的分割方法,但医生进行像素级标注耗时且昂贵。基础视觉模型如分割一切模型(SAM)表现优异,但直接应用于医学图像分割时因缺乏领域知识而效果不佳。本文提出BiSeg-SAM,一种基于SAM的弱监督提示与边界精修框架,用于肠息肉和皮肤病变分割。具体地,我们微调结合CNN模块的SAM以学习局部特征;引入弱框(WeakBox)实现自动框提示生成,并采用多选掩码转框(MM2B)完成粗略掩码到框的转换,缓解粗标签与精细预测间的不匹配问题;同时应用尺度一致性(SC)损失实现预测尺度对齐。此外,细节精修(DetailRefine)模块利用少量真实标签对粗分割结果进行边界优化,显著提升精度。该综合方法在五个肠息肉数据集和一个皮肤癌数据集上均显著优于当前最优方法。
原文摘要 · Abstract (English)
Accurate segmentation of polyps and skin lesions is essential for diagnosing colorectal and skin cancers. While various segmentation methods for polyps and skin lesions using fully supervised deep learning techniques have been developed, the pixel-level annotation of medical images by doctors is both time-consuming and costly. Foundational vision models like the Segment Anything Model (SAM) have demonstrated superior performance; however, directly applying SAM to medical segmentation may not yield satisfactory results due to the lack of domain-specific medical knowledge. In this paper, we propose BiSeg-SAM, a SAM-guided weakly supervised prompting and boundary refinement network for the segmentation of polyps and skin lesions. Specifically, we fine-tune SAM combined with a CNN module to learn local features. We introduce a WeakBox with two functions: automatically generating box prompts for the SAM model and using our proposed Multi-choice Mask-to-Box (MM2B) transformation for rough mask-to-box conversion, addressing the mismatch between coarse labels and precise predictions. Additionally, we apply scale consistency (SC) loss for prediction scale alignment. Our DetailRefine module enhances boundary precision and segmentation accuracy by refining coarse predictions using a limited amount of ground truth labels. This comprehensive approach enables BiSeg-SAM to achieve excellent multi-task segmentation performance. Our method demonstrates significant superiority over state-of-the-art (SOTA) methods when tested on five polyp datasets and one skin cancer dataset.
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