Organizations: Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China · South China University of Technology, Guangzhou, China · CyPhi(ΨΦ) AI Research Lab, School of IT, Monash University Malaysia · Department of Electronic & Computer Engineering, The Hong Kong University of Science and Technology
Abstract
While lightweight polyp segmentation is highly desirable for low-cost deployment, reported performance gains often stem from upgraded backbone encoders, complex decoders, or heavy refinement branches. Consequently, it remains difficult to isolate whether a lightweight correction mechanism is inherently effective on its own. We address this limitation by formulating refinement as a prediction-space recursive correction task, introducing a recursive controller that operates directly on backbone logits. Under a fixed recursion budget, this controller aggregates discrepancy and uncertainty evidence, updates a compact state tracking recent correction utility, and applies additive residual logit corrections. By design, this correction path remains small, host-portable, and deployment-explicit. Utilizing a unified Kvasir-trained protocol, we evaluate our approach across seven lightweight backbones on Kvasir-SEG and three transfer datasets, measuring segmentation accuracy (Dice/IoU) alongside deployment efficiency (parameters, GMACs, and peak memory). The controller yields consistent improvements in the source domain, achieves competitive performance against both training-side baselines and heavier structural refiners on representative hosts, and delivers selective transfer gains with minimal static overhead. Code is available at https://github.com/tyui99/Gain-Aware-Prediction-Space-Recursive-Controller.
Post-refinement can improve colonoscopy segmentation after host inference, but many designs still rely on extra correction heads or multi-stage pipelines with non-negligible parameter or computational cost. For polyp segmentation, host predictions are often already reasonable globally, with remaining errors clustered around ambiguous boundaries and difficult local structures. These residual errors matter in colonoscopy images because useful masks need correct lesion coverage and clean contour delineation across subtle mucosal transitions. This setting favors selective local repair in prediction space over reprocessing the entire mask. We therefore propose RIGS-Refiner, a lightweight post-refinement plugin for risk-guided recursive refinement in prediction space. Starting from a frozen host anchor prediction, RIGS-Refiner extracts lightweight image priors and prediction cues, applies risk-guided update, and writes back residual corrections through a shared recursive cell. The module adds only +519 parameters and +0.631 GFLOPs, keeping the refinement path compact for deployment. Experiments use Kvasir-SEG for training and Kvasir, ClinicDB, ColonDB, and ETIS for evaluation under two frozen hosts, namely PraNet and SegFormer-B0. Results show consistent gains on both hosts and a favorable efficiency-accuracy trade-off against representative post-refinement methods. Code is available at https://github.com/tyui99/RIGS-Refiner.
Automated polyp segmentation in colonoscopy continues to pose challenges due to substantial appearance variations and indistinct polyp boundaries. Although emerging foundation models (FMs) such as DINOv2, SAM, and OneFormer, demonstrate remarkable generalization capabilities, their direct transfer to the polyp segmentation task and deployment in real-time clinical settings are difficult due to lack of large-scale labeled data and high computational demands. In addition, adopting multiple FMs together raises concerns, even though they encode complementary semantic and structural information. While lightweight models, including U-Net, PraNet and U-Net++, are computationally efficient, they often struggle to generalize across datasets due to limited representational capacity. To address this gap, we propose Lite-Polyp Inductor (Lite-Pi), a novel foundation model induction framework that significantly enhances lightweight polyp segmentation baselines. Our proposed framework generates FM-specific prototype representations and aligns them semantically with the corresponding foundation model priors through reconstruction-based supervision. Subsequently, transformer-based fusion is introduced to highlight the polyp relevant representations, including salient boundary information, while preserving complementary semantic cues. Extensive experiments across five polyp segmentation benchmark datasets demonstrate that Lite-π significantly improves lightweight baselines, achieving superior generalization performance with minimal computational overhead and thereby, offering a practical solution for generalized polyp segmentation. Our code is available at GitHub. https://github.com/lostinrepo/Lite-Pi
Automated polyp segmentation is critical for early colorectal cancer detection and its prevention, yet remains challenging due to weak boundaries, large appearance variations, and limited annotated data. Lightweight segmentation models such as U-Net, U-Net++, and PraNet offer practical efficiency for clinical deployment but struggle to capture the rich semantic and structural cues required for accurate delineation of complex polyp regions. In contrast, large Vision Foundation Models (VFMs), including SAM, OneFormer, Mask2Former, and DINOv2, exhibit strong generalization but transfer poorly to polyp segmentation due to domain mismatch, insufficient boundary sensitivity, and high computational cost. To bridge this gap, we propose \textit{\textbf{LiteBounD}, a \underline{Li}gh\underline{t}w\underline{e}ight \underline{Boun}dary-guided \underline{D}istillation} framework that transfers complementary semantic and structural priors from multiple VFMs into compact segmentation backbones. LiteBounD introduces (i) a dual-path distillation mechanism that disentangles semantic and boundary-aware representations, (ii) a frequency-aware alignment strategy that supervises low-frequency global semantics and high-frequency boundary details separately, and (iii) a boundary-aware decoder that fuses multi-scale encoder features with distilled semantically rich boundary information for precise segmentation. Extensive experiments on both seen (Kvasir-SEG, CVC-ClinicDB) and unseen (ColonDB, CVC-300, ETIS) datasets demonstrate that LiteBounD consistently outperforms its lightweight baselines by a significant margin and achieves performance competitive with state-of-the-art methods, while maintaining the efficiency required for real-time clinical use. Our code is available at https://github.com/lostinrepo/LiteBounD.