Clinical Inspired MRI Lesion Segmentation
Lijun Yan, Churan Wang, Fangwei Zhong, Yizhou Wang
TL;DR
The paper tackles MRI lesion segmentation across pre- and post-contrast T1-weighted sequences, a challenging task due to diverse enhancement patterns. It introduces a residual fusion framework with a dual-branch encoder (main post-contrast and auxiliary pre-contrast) and a multi-scale fusion strategy, formalized by the residual block $H(x)=E(x_{ ext{main}})+x_{ ext{aux}}$. A lightweight dynamic weighting mechanism using a 1×1×1 convolution optimizes auxiliary contributions without substantial parameter overhead, enabling robust performance across scales. Empirically, the method achieves state-of-the-art results on BraTS2023 brain tumor segmentation and an in-house breast MRI dataset, with clear improvements in small or irregular lesions and reduced false positives, underscoring its clinically relevant potential.
Abstract
Magnetic resonance imaging (MRI) is a potent diagnostic tool for detecting pathological tissues in various diseases. Different MRI sequences have different contrast mechanisms and sensitivities for different types of lesions, which pose challenges to accurate and consistent lesion segmentation. In clinical practice, radiologists commonly use the sub-sequence feature, i.e. the difference between post contrast-enhanced T1-weighted (post) and pre-contrast-enhanced (pre) sequences, to locate lesions. Inspired by this, we propose a residual fusion method to learn subsequence representation for MRI lesion segmentation. Specifically, we iteratively and adaptively fuse features from pre- and post-contrast sequences at multiple resolutions, using dynamic weights to achieve optimal fusion and address diverse lesion enhancement patterns. Our method achieves state-of-the-art performances on BraTS2023 dataset for brain tumor segmentation and our in-house breast MRI dataset for breast lesion segmentation. Our method is clinically inspired and has the potential to facilitate lesion segmentation in various applications.
