TY - JOUR
T1 - LGPS: A lightweight GAN-based approach for polyp segmentation in colonoscopy images
AU - Tesema, Fiseha Berhanu
AU - Guerra-Manzanares, Alejandro
AU - Cui, Tianxiang
AU - Zhang, Qian
AU - Solomon, Moses M.
AU - He, Xiangjian
PY - 2026/6
Y1 - 2026/6
N2 - Accurate and real-time polyp segmentation is essential for early colorectal cancer detection, yet remains challenging due to small, low-contrast lesions and the computational demands of many deep learning models. We propose LGPS, a Lightweight GAN-based Polyp Segmentation framework that achieves high segmentation accuracy with minimal computational overhead. LGPS integrates a MobileNetV2-based generator enhanced with Residual Squeeze-and-Excitation (ReSE) blocks and a discriminator equipped with Convolutional Conditional Random Fields (ConvCRF) to refine spatial coherence and boundary precision. A hybrid loss function — combining Binary Cross-Entropy, Weighted IoU, and Dice Loss — improves class imbalance handling and sensitivity to small or blurry polyps. LGPS is an extremely compact model, requiring only 1.07 million parameters — over 17smaller than many recent transformer- and CNN-based SOTA architectures — while preserving high segmentation accuracy. In quantitative evaluation, LGPS achieves a Dice score of 0.7299 and an IoU of 0.7867 on the multi-center PolypGen dataset, the most challenging benchmark in polyp segmentation. On the widely used CVC-ClinicDB dataset, LGPS attains the highest IoU (0.9238) among lightweight and transformer-based approaches. The model also runs at 100.08 FPS on 256 × 256 inputs, demonstrating true real-time capability. Stratified evaluation and qualitative results further confirm its robustness on small and low-contrast lesions. These results highlight LGPS as a computationally efficient yet high-performing framework suitable for real-time clinical deployment. The code is available at https://github.com/Falmi/LGPS/
AB - Accurate and real-time polyp segmentation is essential for early colorectal cancer detection, yet remains challenging due to small, low-contrast lesions and the computational demands of many deep learning models. We propose LGPS, a Lightweight GAN-based Polyp Segmentation framework that achieves high segmentation accuracy with minimal computational overhead. LGPS integrates a MobileNetV2-based generator enhanced with Residual Squeeze-and-Excitation (ReSE) blocks and a discriminator equipped with Convolutional Conditional Random Fields (ConvCRF) to refine spatial coherence and boundary precision. A hybrid loss function — combining Binary Cross-Entropy, Weighted IoU, and Dice Loss — improves class imbalance handling and sensitivity to small or blurry polyps. LGPS is an extremely compact model, requiring only 1.07 million parameters — over 17smaller than many recent transformer- and CNN-based SOTA architectures — while preserving high segmentation accuracy. In quantitative evaluation, LGPS achieves a Dice score of 0.7299 and an IoU of 0.7867 on the multi-center PolypGen dataset, the most challenging benchmark in polyp segmentation. On the widely used CVC-ClinicDB dataset, LGPS attains the highest IoU (0.9238) among lightweight and transformer-based approaches. The model also runs at 100.08 FPS on 256 × 256 inputs, demonstrating true real-time capability. Stratified evaluation and qualitative results further confirm its robustness on small and low-contrast lesions. These results highlight LGPS as a computationally efficient yet high-performing framework suitable for real-time clinical deployment. The code is available at https://github.com/Falmi/LGPS/
KW - Polyp segmentation
KW - Generative adversarial networks
KW - Convolutional CRF
KW - Hybrid loss
KW - Real-time medical image analysis
KW - Lightweight model
KW - Colonoscopy
UR - https://doi.org/10.1016/j.bspc.2026.109777
U2 - 10.1016/j.bspc.2026.109777
DO - 10.1016/j.bspc.2026.109777
M3 - Article
SN - 1746-8094
VL - 118
JO - Biomedical Signal Processing and Control
JF - Biomedical Signal Processing and Control
M1 - 109777
ER -