X-ray Computed Laminography (CL) is essential for non-destructive inspection of plate-like structures in applications such as microchips and composite battery materials, where traditional computed tomography (CT) struggles due to geometric constraints. However, reconstructing high-quality volumes from laminographic projections remains challenging, particularly under highly sparse-view acquisition conditions. In this paper, we propose a reconstruction algorithm, namely LamiGauss, that combines Gaussian Splatting radiative rasterization with a dedicated detector-to-world transformation model incorporating the laminographic tilt angle. LamiGauss leverages an initialization strategy that explicitly filters out common laminographic artifacts from the preliminary reconstruction, preventing redundant Gaussians from being allocated to false structures and thereby concentrating model capacity on representing the genuine object. Our approach effectively optimizes directly from sparse projections, enabling accurate and efficient reconstruction with limited data. Extensive experiments on both synthetic and real datasets demonstrate the effectiveness and superiority of the proposed method over existing techniques. LamiGauss uses only 3$\%$ of full views to achieve superior performance over the iterative method optimized on a full dataset.

Sparse-View CT (SVCT) reconstruction enhances temporal resolution and reduces radiation dose, yet its clinical use is hindered by artifacts due to view reduction and domain shifts from scanner, protocol, or anatomical variations, leading to performance degradation in out-of-distribution (OOD) scenarios. In this work, we propose a Cross-Distribution Diffusion Priors-Driven Iterative Reconstruction (CDPIR) framework to tackle the OOD problem in SVCT. CDPIR integrates cross-distribution diffusion priors, derived from a Scalable Interpolant Transformer (SiT), with model-based iterative reconstruction methods. Specifically, we train a SiT backbone, an extension of the Diffusion Transformer (DiT) architecture, to establish a unified stochastic interpolant framework, leveraging Classifier-Free Guidance (CFG) across multiple datasets. By randomly dropping the conditioning with a null embedding during training, the model learns both domain-specific and domain-invariant priors, enhancing generalizability. During sampling, the globally sensitive transformer-based diffusion model exploits the cross-distribution prior within the unified stochastic interpolant framework, enabling flexible and stable control over multi-distribution-to-noise interpolation paths and decoupled sampling strategies, thereby improving adaptation to OOD reconstruction. By alternating between data fidelity and sampling updates, our model achieves state-of-the-art performance with superior detail preservation in SVCT reconstructions. Extensive experiments demonstrate that CDPIR significantly outperforms existing approaches, particularly under OOD conditions, highlighting its robustness and potential clinical value in challenging imaging scenarios.

Fontan palliation for univentricular congenital heart disease progresses to hemodynamic failure with complex flow patterns poorly characterized by conventional 2D imaging. Current assessment relies on fluoroscopic angiography, providing limited 3D geometric information essential for computational fluid dynamics (CFD) analysis and surgical planning. A multi-step AI pipeline was developed utilizing Google's Gemini 2.5 Flash (2.5B parameters) for systematic, iterative processing of fluoroscopic angiograms through transformer-based neural architecture. The pipeline encompasses medical image preprocessing, vascular segmentation, contrast enhancement, artifact removal, and virtual hemodynamic flow visualization within 2D projections. Final views were processed through Tencent's Hunyuan3D-2mini (384M parameters) for stereolithography file generation. The pipeline successfully generated geometrically optimized 2D projections from single-view angiograms after 16 processing steps using a custom web interface. Initial iterations contained hallucinated vascular features requiring iterative refinement to achieve anatomically faithful representations. Final projections demonstrated accurate preservation of complex Fontan geometry with enhanced contrast suitable for 3D conversion. AI-generated virtual flow visualization identified stagnation zones in central connections and flow patterns in branch arteries. Complete processing required under 15 minutes with second-level API response times. This approach demonstrates clinical feasibility of generating CFD-suitable geometries from routine angiographic data, enabling 3D generation and rapid virtual flow visualization for cursory insights prior to full CFD simulation. While requiring refinement cycles for accuracy, this establishes foundation for democratizing advanced geometric and hemodynamic analysis using readily available imaging data.

The utility of Magnetic Resonance Imaging (MRI) in anomaly detection and disease diagnosis is well recognized. However, the current imaging protocol is often hindered by long scanning durations and a misalignment between the scanning process and the specific requirements of subsequent clinical assessments. While recent studies have actively explored accelerated MRI techniques, the majority have concentrated on improving overall image quality across all voxel locations, overlooking the attention to specific abnormalities that hold clinical significance. To address this discrepancy, we propose a model-unrolled deep-learning method, guided by weakly supervised lesion attention, for accelerated MRI oriented by downstream clinical needs. In particular, we construct a lesion-focused MRI reconstruction model, which incorporates customized learnable regularizations that can be learned efficiently by using only image-level labels to improve potential lesion reconstruction but preserve overall image quality. We then design a dedicated iterative algorithm to solve this task-driven reconstruction model, which is further unfolded as a cascaded deep network for lesion-focused fast imaging. Comprehensive experiments on two public datasets, i.e., fastMRI and Stanford Knee MRI Multi-Task Evaluation (SKM-TEA), demonstrate that our approach, referred to as Lesion-Focused MRI (LF-MRI), surpassed existing accelerated MRI methods by relatively large margins. Remarkably, LF-MRI led to substantial improvements in areas showing pathology. The source code and pretrained models will be publicly available at https://github.com/ladderlab-xjtu/LF-MRI.

To investigate the imaging performance of deep-learning reconstruction on multiplexed sensitivity encoding (MUSE DL) compared to single-shot diffusion-weighted imaging (SS-DWI) in the breast. In this prospective, institutional review board-approved study, both single-shot (SS-DWI) and multi-shot MUSE DWI were performed on patients. MUSE DWI was processed using deep-learning reconstruction (MUSE DL). Quantitative analysis included calculating apparent diffusion coefficients (ADCs), signal-to-noise ratio (SNR) within fibroglandular tissue (FGT), adjacent pectoralis muscle, and breast tumors. The Hausdorff distance (HD) was used as a distortion index to compare breast contours between T2-weighted anatomical images, SS-DWI, and MUSE images. Subjective visual qualitative analysis was performed using Likert scale. Quantitative analyses were assessed using Friedman's rank-based analysis with Bonferroni correction. Sixty-one female participants (mean age 49.07 years ± 11.0 [standard deviation]; age range 23-75 years) with 65 breast lesions were included in this study. All data were acquired using a 3 T MRI scanner. The MUSE DL yielded significant improvement in image quality compared with non-DL MUSE in both 2-shot and 4-shot settings (SNR enhancement FGT 2-shot DL 207.8 % [125.5-309.3],4- shot DL 175.1 % [102.2-223.5]). No significant difference was observed in the ADC between MUSE, MUSE DL, and SS-DWI in both benign (P = 0.154) and malignant tumors (P = 0.167). There was significantly less distortion in the 2- and 4-shot MUSE DL images (HD 3.11 mm, 2.58 mm) than in the SS-DWI images (4.15 mm, P < 0.001). MUSE DL enhances SNR, minimizes image distortion, and preserves lesion diagnosis accuracy and ADC values.

Deep learning-based super-resolution (SR) reconstruction can obtain high-quality images with more detailed information. To compare multiparametric normal-resolution (NR) and SR magnetic resonance imaging (MRI) in predicting the histopathologic grade in hepatocellular carcinoma. We retrospectively analyzed a total of 826 patients from two medical centers (training 459; validation 196; test 171). T2-weighted imaging, diffusion-weighted imaging, and portal venous phases were collected. Tumor segmentations were conducted automatically by 3D U-Net. Based on generative adversarial network, we utilized 3D SR reconstruction to produce SR MRI. Radiomics models were developed and validated by XGBoost and Catboost. The predictive efficiency was demonstrated by calibration curves, decision curve analysis, area under the curve (AUC) and net reclassification index (NRI). We extracted 3045 radiomic features from both NR and SR MRI, retaining 29 and 28 features, respectively. For XGBoost models, SR MRI yielded higher AUC value than NR MRI in the validation and test cohorts (0.83 <i>vs</i> 0.79; 0.80 <i>vs</i> 0.78), respectively. Consistent trends were seen in CatBoost models: SR MRI achieved AUCs of 0.89 and 0.80 compared to NR MRI's 0.81 and 0.76. NRI indicated that the SR MRI models could improve the prediction accuracy by -1.6% to 20.9% compared to the NR MRI models. Deep learning-based SR MRI could improve the predictive performance of histopathologic grade in HCC. It may be a powerful tool for better stratification management for patients with operable HCC.

Missing input sequences are common in medical imaging data, posing a challenge for deep learning models reliant on complete input data. In this work, inspired by MultiMAE [2], we develop a masked autoencoder (MAE) paradigm for multi-modal, multi-task learning in 3D medical imaging with brain MRIs. Our method treats each MRI sequence as a separate input modality, leveraging a late-fusion-style transformer encoder to integrate multi-sequence information (multi-modal) and individual decoder streams for each modality for multi-task reconstruction. This pretraining strategy guides the model to learn rich representations per modality while also equipping it to handle missing inputs through cross-sequence reasoning. The result is a flexible and generalizable encoder for brain MRIs that infers missing sequences from available inputs and can be adapted to various downstream applications. We demonstrate the performance and robustness of our method against an MAE-ViT baseline in downstream segmentation and classification tasks, showing absolute improvement of $10.1$ overall Dice score and $0.46$ MCC over the baselines with missing input sequences. Our experiments demonstrate the strength of this pretraining strategy. The implementation is made available.

To develop a volume of interest (VOI) imaging technique in multi-detector-row helical CT to reduce radiation dose or improve image quality within the VOI. A deep-learning method based on a residual U-Net architecture, named VOI-Net, was developed to correct truncation artifacts in VOI helical CT. Three patient cases, a chest CT of interstitial lung disease and 2 abdominopelvic CT of liver tumour, were used for evaluation through simulation. VOI-Net effectively corrected truncation artifacts (root mean square error [RMSE] of 5.97 ± 2.98 Hounsfield Units [HU] for chest, 3.12 ± 1.93 HU, and 3.71 ± 1.87 HU for liver). Radiation dose was reduced by 71% without sacrificing image quality within a 10-cm diameter VOI, compared to a full scan field of view (FOV) of 50 cm. With the same total energy deposited as in a full FOV scan, image quality within the VOI matched that at 350% higher radiation dose. A radiologist confirmed improved lesion conspicuity and visibility of small linear reticulations associated with ground-glass opacity and liver tumour. Focusing radiation on the VOI and using VOI-Net in a helical scan, total radiation can be reduced or higher image quality equivalent to those at higher doses in standard full FOV scan can be achieved within the VOI. A targeted helical VOI imaging technique enabled by a deep-learning-based artifact correction method improves image quality within the VOI without increasing radiation dose.

Rigid-motion artifacts, such as cortical bone streaking and trabecular smearing, hinder in vivo assessment of bone microstructures in high-resolution peripheral quantitative computed tomography (HR-pQCT). Despite various motion grading techniques, no motion correction methods exist due to the lack of standardized degradation models. We optimize a conventional sinogram-based method to simulate motion artifacts in HR-pQCT images, creating paired datasets of motion-corrupted images and their corresponding ground truth, which enables seamless integration into supervised learning frameworks for motion correction. As such, we propose an Edge-enhanced Self-attention Wasserstein Generative Adversarial Network with Gradient Penalty (ESWGAN-GP) to address motion artifacts in both simulated (source) and real-world (target) datasets. The model incorporates edge-enhancing skip connections to preserve trabecular edges and self-attention mechanisms to capture long-range dependencies, facilitating motion correction. A visual geometry group (VGG)-based perceptual loss is used to reconstruct fine micro-structural features. The ESWGAN-GP achieves a mean signal-to-noise ratio (SNR) of 26.78, structural similarity index measure (SSIM) of 0.81, and visual information fidelity (VIF) of 0.76 for the source dataset, while showing improved performance on the target dataset with an SNR of 29.31, SSIM of 0.87, and VIF of 0.81. The proposed methods address a simplified representation of real-world motion that may not fully capture the complexity of in vivo motion artifacts. Nevertheless, because motion artifacts present one of the foremost challenges to more widespread adoption of this modality, these methods represent an important initial step toward implementing deep learning-based motion correction in HR-pQCT.

Three-dimensional ultrasound (US) offers many clinical advantages over conventional 2D imaging, yet its widespread adoption is limited by the cost and complexity of traditional 3D systems. Sensorless 3D US, which uses deep learning to estimate a 3D probe trajectory from a sequence of 2D US images, is a promising alternative. Local features, such as speckle patterns, can help predict frame-to-frame motion, while global features, such as coarse shapes and anatomical structures, can situate the scan relative to anatomy and help predict its general shape. In prior approaches, global features are either ignored or tightly coupled with local feature extraction, restricting the ability to robustly model these two complementary aspects. We propose DualTrack, a novel dual-encoder architecture that leverages decoupled local and global encoders specialized for their respective scales of feature extraction. The local encoder uses dense spatiotemporal convolutions to capture fine-grained features, while the global encoder utilizes an image backbone (e.g., a 2D CNN or foundation model) and temporal attention layers to embed high-level anatomical features and long-range dependencies. A lightweight fusion module then combines these features to estimate the trajectory. Experimental results on a large public benchmark show that DualTrack achieves state-of-the-art accuracy and globally consistent 3D reconstructions, outperforming previous methods and yielding an average reconstruction error below 5 mm.