Lightweight Relational Embedding in Task-Interpolated Few-Shot Networks for Enhanced Gastrointestinal Disease Classification

Traditional diagnostic methods like colonoscopy are invasive yet critical tools necessary for accurately diagnosing colorectal cancer (CRC). Detection of CRC at early stages is crucial for increasing patient survival rates. However, colonoscopy is dependent on obtaining adequate and high-quality endoscopic images. Prolonged invasive procedures are inherently risky for patients, while suboptimal or insufficient images hamper diagnostic accuracy. These images, typically derived from video frames, often exhibit similar patterns, posing challenges in discrimination. To overcome these challenges, we propose a novel Deep Learning network built on a Few-Shot Learning architecture, which includes a tailored feature extractor, task interpolation, relational embedding, and a bi-level routing attention mechanism. The Few-Shot Learning paradigm enables our model to rapidly adapt to unseen fine-grained endoscopic image patterns, and the task interpolation augments the insufficient images artificially from varied instrument viewpoints. Our relational embedding approach discerns critical intra-image features and captures inter-image transitions between consecutive endoscopic frames, overcoming the limitations of Convolutional Neural Networks (CNNs). The integration of a light-weight attention mechanism ensures a concentrated analysis of pertinent image regions. By training on diverse datasets, the model's generalizability and robustness are notably improved for handling endoscopic images. Evaluated on Kvasir dataset, our model demonstrated superior performance, achieving an accuracy of 90.1\%, precision of 0.845, recall of 0.942, and an F1 score of 0.891. This surpasses current state-of-the-art methods, presenting a promising solution to the challenges of invasive colonoscopy by optimizing CRC detection through advanced image analysis.

Contrast-Invariant Self-supervised Segmentation for Quantitative Placental MRI

Accurate placental segmentation is essential for quantitative analysis of the placenta. However, this task is particularly challenging in T2*-weighted placental imaging due to: (1) weak and inconsistent boundary contrast across individual echoes; (2) the absence of manual ground truth annotations for all echo times; and (3) motion artifacts across echoes caused by fetal and maternal movement. In this work, we propose a contrast-augmented segmentation framework that leverages complementary information across multi-echo T2*-weighted MRI to learn robust, contrast-invariant representations. Our method integrates: (i) masked autoencoding (MAE) for self-supervised pretraining on unlabeled multi-echo slices; (ii) masked pseudo-labeling (MPL) for unsupervised domain adaptation across echo times; and (iii) global-local collaboration to align fine-grained features with global anatomical context. We further introduce a semantic matching loss to encourage representation consistency across echoes of the same subject. Experiments on a clinical multi-echo placental MRI dataset demonstrate that our approach generalizes effectively across echo times and outperforms both single-echo and naive fusion baselines. To our knowledge, this is the first work to systematically exploit multi-echo T2*-weighted MRI for placental segmentation.