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arXiv 2603.04565cs.CV
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基于结构引导的组织病理学合成 via 双LoRA扩散

Structure-Guided Histopathology Synthesis via Dual-LoRA Diffusion

Stony Brook University(石溪大学)

Xuan Xu, Prateek Prasanna

AI总结:

本文提出Dual-LoRA可控扩散框架,通过多类核质心和LoRA适配器实现局部结构修复与全局结构合成,提升组织病理学图像的真实感和一致性。

摘要:

组织病理学图像合成在组织修复、数据增强和肿瘤微环境建模中起着重要作用。然而,现有的生成方法通常将修复和生成作为单独的任务处理,尽管两者共享相同的客观目标,即在不同程度的缺失情况下实现结构一致的组织合成,并且经常依赖于弱或不一致的结构先验,这限制了真实的细胞组织结构。我们提出了Dual-LoRA可控扩散,一种统一的质心引导扩散框架,该框架在单个模型中联合支持局部结构修复和全局结构合成。多类核质心作为轻量且标注高效的空域先验,能够在部分和完整图像缺失的情况下提供生物上有意义的指导。两个任务特定的LoRA适配器专门化共享的主干,用于局部和全局目标,而无需重新训练单独的扩散模型。广泛的实验表明,在修复和合成任务中,与最先进GAN和扩散基线相比,有显著的改进。对于局部修复,计算在遮蔽区域内的LPIPS值从0.1797(HARP)提高到0.1524,而对于全局合成,FID值从225.15(CoSys)提高到76.04,表明结构保真度和真实感的提高。我们的方法在遮蔽区域实现了更忠实的结构恢复,并在完整合成中显著提高了真实感和形态一致性,支持可扩展的全癌症组织病理学建模。

英文摘要:

Histopathology image synthesis plays an important role in tissue restoration, data augmentation, and modeling of tumor microenvironments. However, existing generative methods typically address restoration and generation as separate tasks, although both share the same objective of structure-consistent tissue synthesis under varying degrees of missingness, and often rely on weak or inconsistent structural priors that limit realistic cellular organization. We propose Dual-LoRA Controllable Diffusion, a unified centroid-guided diffusion framework that jointly supports Local Structure Completion and Global Structure Synthesis within a single model. Multi-class nuclei centroids serve as lightweight and annotation-efficient spatial priors, providing biologically meaningful guidance under both partial and complete image absence. Two task-specific LoRA adapters specialize the shared backbone for local and global objectives without retraining separate diffusion models. Extensive experiments demonstrate consistent improvements over state-of-the-art GAN and diffusion baselines across restoration and synthesis tasks. For local completion, LPIPS computed within the masked region improves from 0.1797 (HARP) to 0.1524, and for global synthesis, FID improves from 225.15 (CoSys) to 76.04, indicating improved structural fidelity and realism. Our approach achieves more faithful structural recovery in masked regions and substantially improved realism and morphology consistency in full synthesis, supporting scalable pan-cancer histopathology modeling.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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