Abstract:In multi-class histopathology nuclei analysis tasks, the lack of training data becomes a main bottleneck for the performance of learning-based methods. To tackle this challenge, previous methods have utilized generative models to increase data by generating synthetic samples. However, existing methods often overlook the importance of considering the context of biological tissues (e.g., shape, spatial layout, and tissue type) in the synthetic data. Moreover, while generative models have shown superior performance in synthesizing realistic histopathology images, none of the existing methods are capable of producing image-label pairs at the same time. In this paper, we introduce a novel framework for co-synthesizing histopathology nuclei images and paired semantic labels using a context-conditioned joint diffusion model. We propose conditioning of a diffusion model using nucleus centroid layouts with structure-related text prompts to incorporate spatial and structural context information into the generation targets. Moreover, we enhance the granularity of our synthesized semantic labels by generating instance-wise nuclei labels using distance maps synthesized concurrently in conjunction with the images and semantic labels. We demonstrate the effectiveness of our framework in generating high-quality samples on multi-institutional, multi-organ, and multi-modality datasets. Our synthetic data consistently outperforms existing augmentation methods in the downstream tasks of nuclei segmentation and classification.
Abstract:With the emergence of the Segment Anything Model (SAM) as a foundational model for image segmentation, its application has been extensively studied across various domains, including the medical field. However, its potential in the context of histopathology data, specifically in region segmentation, has received relatively limited attention. In this paper, we evaluate SAM's performance in zero-shot and fine-tuned scenarios on histopathology data, with a focus on interactive segmentation. Additionally, we compare SAM with other state-of-the-art interactive models to assess its practical potential and evaluate its generalization capability with domain adaptability. In the experimental results, SAM exhibits a weakness in segmentation performance compared to other models while demonstrating relative strengths in terms of inference time and generalization capability. To improve SAM's limited local refinement ability and to enhance prompt stability while preserving its core strengths, we propose a modification of SAM's decoder. The experimental results suggest that the proposed modification is effective to make SAM useful for interactive histology image segmentation. The code is available at \url{https://github.com/hvcl/SAM_Interactive_Histopathology}
Abstract:Tumor region segmentation is an essential task for the quantitative analysis of digital pathology. Recently presented deep neural networks have shown state-of-the-art performance in various image-segmentation tasks. However, because of the unclear boundary between the cancerous and normal regions in pathology images, despite using modern methods, it is difficult to produce satisfactory segmentation results in terms of the reliability and accuracy required for medical data. In this study, we propose an interactive segmentation method that allows users to refine the output of deep neural networks through click-type user interactions. The primary method is to formulate interactive segmentation as an optimization problem that leverages both user-provided click constraints and semantic information in a feature map using a click-guided attention module (CGAM). Unlike other existing methods, CGAM avoids excessive changes in segmentation results, which can lead to the overfitting of user clicks. Another advantage of CGAM is that the model size is independent of input image size. Experimental results on pathology image datasets indicated that our method performs better than existing state-of-the-art methods.