IVAICVMay 29, 2025

Synthetic Generation and Latent Projection Denoising of Rim Lesions in Multiple Sclerosis

arXiv:2505.23353v11 citationsh-index: 24Has Code
Originality Incremental advance
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This work addresses the challenge of rare lesion detection in medical imaging for multiple sclerosis diagnosis, representing an incremental advancement with domain-specific applications.

The paper tackled the class imbalance problem in detecting paramagnetic rim lesions (PRLs) in multiple sclerosis by generating synthetic quantitative susceptibility maps and introducing a denoising method, resulting in improved classifier performance and better approximation of the unseen rim lesion distribution.

Quantitative susceptibility maps from magnetic resonance images can provide both prognostic and diagnostic information in multiple sclerosis, a neurodegenerative disease characterized by the formation of lesions in white matter brain tissue. In particular, susceptibility maps provide adequate contrast to distinguish between "rim" lesions, surrounded by deposited paramagnetic iron, and "non-rim" lesion types. These paramagnetic rim lesions (PRLs) are an emerging biomarker in multiple sclerosis. Much effort has been devoted to both detection and segmentation of such lesions to monitor longitudinal change. As paramagnetic rim lesions are rare, addressing this problem requires confronting the class imbalance between rim and non-rim lesions. We produce synthetic quantitative susceptibility maps of paramagnetic rim lesions and show that inclusion of such synthetic data improves classifier performance and provide a multi-channel extension to generate accompanying contrasts and probabilistic segmentation maps. We exploit the projection capability of our trained generative network to demonstrate a novel denoising approach that allows us to train on ambiguous rim cases and substantially increase the minority class. We show that both synthetic lesion synthesis and our proposed rim lesion label denoising method best approximate the unseen rim lesion distribution and improve detection in a clinically interpretable manner. We release our code and generated data at https://github.com/agr78/PRLx-GAN upon publication.

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