While Vision-Language Models (VLMs) have achieved notable progress in computational pathology (CPath), the gigapixel scale and spatial heterogeneity of Whole Slide Images (WSIs) continue to pose challenges for multimodal understanding. Existing alignment methods struggle to capture fine-grained correspondences between textual descriptions and visual cues across thousands of patches from a slide, compromising their performance on downstream tasks. In this paper, we propose PathFLIP (Pathology Fine-grained Language-Image Pretraining), a novel framework for holistic WSI interpretation. PathFLIP decomposes slide-level captions into region-level sub-captions and generates text-conditioned region embeddings to facilitate precise visual-language grounding. By harnessing Large Language Models (LLMs), PathFLIP can seamlessly follow diverse clinical instructions and adapt to varied diagnostic contexts. Furthermore, it exhibits versatile capabilities across multiple paradigms, efficiently handling slide-level classification and retrieval, fine-grained lesion localization, and instruction following. Extensive experiments demonstrate that PathFLIP outperforms existing large-scale pathological VLMs on four representative benchmarks while requiring significantly less training data, paving the way for fine-grained, instruction-aware WSI interpretation in research and clinical practice.

Panoramic segmentation of renal pathological tissues plays a crucial role in diagnosing renal carcinoma and other kidney-related diseases. The multi-scale nature of kidney tissues, which requires different magnification levels for accurate analysis, presents a significant challenge for segmentation models. In this work, we propose a Multi-scale Context Intertwining Network (MCINet) to address this issue. Our approach utilizes an auxiliary interaction network to enhance feature interaction between different scales and generate pseudo-labels for unannotated structures. By incorporating exponential moving average strategies, we ensure seamless feature integration across scales. Extensive experiments demonstrate that MCINet outperforms state-of-the-art models in key metrics such as Dice and Hausdorff Distance, proving its efficacy in renal tissue segmentation tasks.

Given an object mask, Semi-supervised Video Object Segmentation (SVOS) technique aims to track and segment the object across video frames, serving as a fundamental task in computer vision. Although recent memory-based methods demonstrate potential, they often struggle with scenes involving occlusion, particularly in handling object interactions and high feature similarity. To address these issues and meet the real-time processing requirements of downstream applications, in this paper, we propose a novel bOundary Amendment video object Segmentation method with Inherent Structure refinement, hereby named OASIS. Specifically, a lightweight structure refinement module is proposed to enhance segmentation accuracy. With the fusion of rough edge priors captured by the Canny filter and stored object features, the module can generate an object-level structure map and refine the representations by highlighting boundary features. Evidential learning for uncertainty estimation is introduced to further address challenges in occluded regions. The proposed method, OASIS, maintains an efficient design, yet extensive experiments on challenging benchmarks demonstrate its superior performance and competitive inference speed compared to other state-of-the-art methods, i.e., achieving the F values of 91.6 (vs. 89.7 on DAVIS-17 validation set) and G values of 86.6 (vs. 86.2 on YouTubeVOS 2019 validation set) while maintaining a competitive speed of 48 FPS on DAVIS.

Cell instance segmentation is critical to analyzing biomedical images, yet accurately distinguishing tightly touching cells remains a persistent challenge. Existing instance segmentation frameworks, including detection-based, contour-based, and distance mapping-based approaches, have made significant progress, but balancing model performance with computational efficiency remains an open problem. In this paper, we propose a novel cell instance segmentation method inspired by the four-color theorem. By conceptualizing cells as countries and tissues as oceans, we introduce a four-color encoding scheme that ensures adjacent instances receive distinct labels. This reformulation transforms instance segmentation into a constrained semantic segmentation problem with only four predicted classes, substantially simplifying the instance differentiation process. To solve the training instability caused by the non-uniqueness of four-color encoding, we design an asymptotic training strategy and encoding transformation method. Extensive experiments on various modes demonstrate our approach achieves state-of-the-art performance. The code is available at https://github.com/zhangye-zoe/FCIS.

Weakly supervised segmentation methods have garnered considerable attention due to their potential to alleviate the need for labor-intensive pixel-level annotations during model training. Traditional weakly supervised nuclei segmentation approaches typically involve a two-stage process: pseudo-label generation followed by network training. The performance of these methods is highly dependent on the quality of the generated pseudo-labels, which can limit their effectiveness. In this paper, we propose a novel domain-adaptive weakly supervised nuclei segmentation framework that addresses the challenge of pseudo-label generation through cross-task interaction strategies. Specifically, our approach leverages weakly annotated data to train an auxiliary detection task, which facilitates domain adaptation of the segmentation network. To improve the efficiency of domain adaptation, we introduce a consistent feature constraint module that integrates prior knowledge from the source domain. Additionally, we develop methods for pseudo-label optimization and interactive training to enhance domain transfer capabilities. We validate the effectiveness of our proposed method through extensive comparative and ablation experiments conducted on six datasets. The results demonstrate that our approach outperforms existing weakly supervised methods and achieves performance comparable to or exceeding that of fully supervised methods. Our code is available athttps://github.com/zhangye-zoe/DAWN.

Nuclei instance segmentation in histopathological images is crucial for biological analysis and cancer diagnosis. However, it faces two significant challenges: (1) poorly stained nuclei can lead to under-segmentation, as the background may be mistakenly identified as the foreground; and (2) deep textures within nuclei often result in fragmented instance predictions, as these textures can be misinterpreted as contours. To address these problems, this paper proposes a Structure Encoding and Interaction NEtwork, termed SEINE, which develops the nuclei structure modeling scheme and takes advantage of the similarity between nuclei structure to improve the integrality of instance segmentation. Specifically, SEINE introduces a contour-based structure encoding mechanism that integrates the correlation between nuclear structure and semantics, enabling a more accurate structural representation. Building on this encoding, we propose a structure-guided attention module, which uses clear nuclei as prototypes to guide the structural learning of unclear nuclei, thereby addressing the under-segmentation problem. Additionally, a position enhancement strategy applies a centroid distance constraint to reduce contour prediction errors, effectively mitigating fragmented instance segmentation. Extensive experiments demonstrate the effectiveness of SEINE, achieving state-of-the-art performance across four benchmark datasets.