提出3D皮肤病变追踪新方法,提升匹配准确率并构建首个大规模数据集
Revisiting Lesion Tracking in 3D Total Body Photography
- 通过模板对齐与流场优化实现跨扫描病变匹配
- 在198名受试者上达到89.9%匹配成功率(10mm标准)
- 适用于皮肤癌早期筛查,尤其适合大量病变场景
黑色素瘤是致命性最强的皮肤癌。追踪全身痣的变化并检测新病灶对早期发现至关重要。尽管已有纵向3D全身摄影病变追踪研究,仍存在三大挑战:1)跨扫描正确匹配病灶的准确性低;2)对噪声检测敏感;3)缺乏包含大量标注病灶对的大规模数据集。本文提出一个框架,输入一对3D纹理网格,实现全身范围内病变匹配并识别无法匹配的病灶。首先将源和目标网格映射到模板网格,生成对应映射图;利用这些映射图在模板域定义源/目标信号,构建对齐信号的流场;再沿该向量场正向/反向推进以精炼初始对应关系;最后基于精炼后的对应关系完成病变分配。我们构建了首个大规模皮肤病变追踪数据集,包含198名受试者、共25,000个病灶对。所提方法在所有标注病灶对上达到89.9%的成功率(10 mm标准),在超过200个病灶的受试者中匹配准确率达98.2%。
原文摘要 · Abstract (English)
Melanoma is the most deadly form of skin cancer. Tracking the evolution of nevi and detecting new lesions across the body is essential for the early detection of melanoma. Despite prior work on longitudinal tracking of skin lesions in 3D total body photography, there are still several challenges, including 1) low accuracy for finding correct lesion pairs across scans, 2) sensitivity to noisy lesion detection, and 3) lack of large-scale datasets with numerous annotated lesion pairs. We propose a framework that takes in a pair of 3D textured meshes, matches lesions in the context of total body photography, and identifies unmatchable lesions. We start by computing correspondence maps bringing the source and target meshes to a template mesh. Using these maps to define source/target signals over the template domain, we construct a flow field aligning the mapped signals. The initial correspondence maps are then refined by advecting forward/backward along the vector field. Finally, lesion assignment is performed using the refined correspondence maps. We propose the first large-scale dataset for skin lesion tracking with 25K lesion pairs across 198 subjects. The proposed method achieves a success rate of 89.9% (at 10 mm criterion) for all pairs of annotated lesions and a matching accuracy of 98.2% for subjects with more than 200 lesions.
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