BARL: Bilateral Alignment in Representation and Label Spaces for Semi-Supervised Volumetric Medical Image Segmentation
Shujian Gao, Yuan Wang, Zekuan Yu
TL;DR
This work tackles the challenge of semi-supervised volumetric medical image segmentation under limited annotations by proposing BARL, a dual-space framework that enforces alignment in both representation and label spaces. It introduces region-level and lesion-instance representation alignment alongside label-space modules DPR and PCBC within a co-training setup, unifying constraints across multiple decoder scales. Extensive experiments across BraTS 2020/2021/2023 MEN, CBCT Tooth, and IXI demonstrate that BARL achieves state-of-the-art performance under 5–20% labeling, with strong Dice and boundary metrics and robust cross-dataset generalization. Ablation studies validate the contribution of each component, including the importance of instance-level representation alignment, multi-level DPR, and uncertainty-guided PCBC, establishing BARL as a powerful baseline for data-efficient 3D medical image segmentation.
Abstract
Semi-supervised medical image segmentation (SSMIS) seeks to match fully supervised performance while sharply reducing annotation cost. Mainstream SSMIS methods rely on \emph{label-space consistency}, yet they overlook the equally critical \emph{representation-space alignment}. Without harmonizing latent features, models struggle to learn representations that are both discriminative and spatially coherent. To this end, we introduce \textbf{Bilateral Alignment in Representation and Label spaces (BARL)}, a unified framework that couples two collaborative branches and enforces alignment in both spaces. For label-space alignment, inspired by co-training and multi-scale decoding, we devise \textbf{Dual-Path Regularization (DPR)} and \textbf{Progressively Cognitive Bias Correction (PCBC)} to impose fine-grained cross-branch consistency while mitigating error accumulation from coarse to fine scales. For representation-space alignment, we conduct region-level and lesion-instance matching between branches, explicitly capturing the fragmented, complex pathological patterns common in medical imagery. Extensive experiments on four public benchmarks and a proprietary CBCT dataset demonstrate that BARL consistently surpasses state-of-the-art SSMIS methods. Ablative studies further validate the contribution of each component. Code will be released soon.
