Pseudo-healthy image synthesis aims to generate subject-specific, pathology-free images from pathological scans. Such images can be helpful in certain tasks, such as anomaly detection and understanding changes induced by pathology and disease. A participant cannot be "healthy" and "unhealthy" at the same time, and thus, directly obtaining pathological and healthy paired images of the same individual to train and evaluate supervised learning algorithms is infeasible. In addition, simultaneously meeting the requirements of subjects' "identity" preservation and pathology restoration performance is frequently difficult for existing unsupervised learning methods, especially for large or information-free pathological regions, such as postoperative cavities. In this study, we propose a novel pseudo-healthy synthesis framework that combines low-resolution residual decoupling with an edge-prior-guided super-resolution reconstruction module. We named this framework LRD-ESR-Net. In particular, by using a coarse-to-fine synthesis pipeline, the residual decoupling network first decouples information-rich tumor tissues or information-free resection cavities from healthy brain tissues in low-resolution pathological magnetic resonance images. Then, a residual-shifting diffusion network with Canny edge maps is employed to reconstruct low-resolution pseudo-healthy images to their original resolutions. We evaluate the proposed framework on one in-house brain dataset, two public brain datasets, and one public liver dataset, and validate its effectiveness on low-contrast lesion segmentation and pre-/postoperative brain tumor MRI registration. Results show that LRD-ESR-Net consistently outperforms state-of-the-art methods in pseudo-healthy image quality, anatomical preservation, and downstream task performance, demonstrating strong robustness and generalization across organs, modalities, and lesion types.

Spine parsing (i.e., multi-class segmentation of vertebrae and intervertebral discs (IVDs)) for volumetric magnetic resonance (MR) image plays a significant role in various spinal disease diagnoses and treatments of spine disorders, yet is still a challenge due to the inter-class similarity and intra-class variation of spine images. Existing fully convolutional network based methods failed to explicitly exploit the dependencies between different spinal structures. In this article, we propose a novel two-stage framework named SpineParseNet to achieve automated spine parsing for volumetric MR images. The SpineParseNet consists of a 3D graph convolutional segmentation network (GCSN) for 3D coarse segmentation and a 2D residual U-Net (ResUNet) for 2D segmentation refinement. In 3D GCSN, region pooling is employed to project the image representation to graph representation, in which each node representation denotes a specific spinal structure. The adjacency matrix of the graph is designed according to the connection of spinal structures. The graph representation is evolved by graph convolutions. Subsequently, the proposed region unpooling module re-projects the evolved graph representation to a semantic image representation, which facilitates the 3D GCSN to generate reliable coarse segmentation. Finally, the 2D ResUNet refines the segmentation. Experiments on T2-weighted volumetric MR images of 215 subjects show that SpineParseNet achieves impressive performance with mean Dice similarity coefficients of 87.32 ± 4.75%, 87.78 ± 4.64%, and 87.49 ± 3.81% for the segmentations of 10 vertebrae, 9 IVDs, and all 19 spinal structures respectively. The proposed method has great potential in clinical spinal disease diagnoses and treatments.

Conducting an accurate motion correction of liver dynamic contrast-enhanced magnetic resonance (DCE-MR) imaging remains challenging because of intensity variations caused by contrast agents. Such variations lead to the failure of the traditional intensity-based registration method. To address this problem, we propose a correlation-weighted sparse representation framework to separate the contrast agent from original liver DCE-MR images. This framework allows the robust registration of motion components over time without intensity variances. Existing sparse coding techniques recover a 3D image containing only contrast agents (named contrast enhancement component) from a manually labeled dictionary, whose column has the same size with the original 3D volume (3D-t mode). The high dimension of the recovery target (3D volume) and the indistinguishability between the unenhanced and enhanced images make accurate coding difficult. In this paper, we predefine an ideal time-intensity curve containing only contrast agents (named contrast agent curve) and recover it from the transpose dictionary (t-3D mode), whose column has been updated into the original time-intensity curves. The low dimension of the target (1D curve) and the significant intergroup difference between contrast agent curves and non-contrast agent curves can estimate a series of pure contrast agent curves. A "correlation-weighted" constraint is introduced for the selection of a coding subset with more contrast agent curves, leading to an efficient and accurate sparse recovery process. Then, the contrast enhancement component can be estimated by the solved sparse coefficients' map and the ideal curve and subtracted from the original DCE-MRI. Finally, we register the de-enhanced images and apply the obtained deformation fields for the original DCE-MRI to achieve the goal of motion correction. We conduct the experiments on both simulated and real liver DCE-MRI data. Compared with other state-of-the-art DCE-MRI registration methods, the experimental results show that our method achieves a better registration performance with less computational efficiency.