Medical image segmentation is crucial for many healthcare tasks, including disease diagnosis and treatment planning. One key area is the segmentation of skin lesions, which is vital for diagnosing skin cancer and monitoring patients. In this context, this paper introduces SegDT, a new segmentation model based on diffusion transformer (DiT). SegDT is designed to work on low-cost hardware and incorporates Rectified Flow, which improves the generation quality at reduced inference steps and maintains the flexibility of standard diffusion models. Our method is evaluated on three benchmarking datasets and compared against several existing works, achieving state-of-the-art results while maintaining fast inference speeds. This makes the proposed model appealing for real-world medical applications. This work advances the performance and capabilities of deep learning models in medical image analysis, enabling faster, more accurate diagnostic tools for healthcare professionals. The code is made publicly available at \href{https://github.com/Bekhouche/SegDT}{GitHub}.

Parameter-efficient fine-tuning (PEFT) of pre-trained foundation models is increasingly attracting interest in medical imaging due to its effectiveness and computational efficiency. Among these methods, Low-Rank Adaptation (LoRA) is a notable approach based on the assumption that the adaptation inherently occurs in a low-dimensional subspace. While it has shown good performance, its implementation requires a fixed and unalterable rank, which might be challenging to select given the unique complexities and requirements of each medical imaging downstream task. Inspired by advancements in natural image processing, we introduce a novel approach for medical image segmentation that dynamically adjusts the intrinsic rank during adaptation. Viewing the low-rank representation of the trainable weight matrices as a singular value decomposition, we introduce an l_1 sparsity regularizer to the loss function, and tackle it with a proximal optimizer. The regularizer could be viewed as a penalty on the decomposition rank. Hence, its minimization enables to find task-adapted ranks automatically. Our method is evaluated in a realistic few-shot fine-tuning setting, where we compare it first to the standard LoRA and then to several other PEFT methods across two distinguishable tasks: base organs and novel organs. Our extensive experiments demonstrate the significant performance improvements driven by our method, highlighting its efficiency and robustness against suboptimal rank initialization. Our code is publicly available: https://github.com/ghassenbaklouti/ARENA

Background: Radiomics shows promise in characterizing glioblastoma, but its added value over clinical and molecular predictors has yet to be proven. This study assessed the added value of conventional radiomics (CR) and deep learning (DL) MRI radiomics for glioblastoma prognosis (<= 6 vs > 6 months survival) on a large multi-center dataset. Methods: After patient selection, our curated dataset gathers 1152 glioblastoma (WHO 2016) patients from five Swiss centers and one public source. It included clinical (age, gender), molecular (MGMT, IDH), and baseline MRI data (T1, T1 contrast, FLAIR, T2) with tumor regions. CR and DL models were developed using standard methods and evaluated on internal and external cohorts. Sub-analyses assessed models with different feature sets (imaging-only, clinical/molecular-only, combined-features) and patient subsets (S-1: all patients, S-2: with molecular data, S-3: IDH wildtype). Results: The best performance was observed in the full cohort (S-1). In external validation, the combined-feature CR model achieved an AUC of 0.75, slightly, but significantly outperforming clinical-only (0.74) and imaging-only (0.68) models. DL models showed similar trends, though without statistical significance. In S-2 and S-3, combined models did not outperform clinical-only models. Exploratory analysis of CR models for overall survival prediction suggested greater relevance of imaging data: across all subsets, combined-feature models significantly outperformed clinical-only models, though with a modest advantage of 2-4 C-index points. Conclusions: While confirming the predictive value of anatomical MRI sequences for glioblastoma prognosis, this multi-center study found standard CR and DL radiomics approaches offer minimal added value over demographic predictors such as age and gender.

High-resolution volumetric computed tomography (CT) is essential for accurate diagnosis and treatment planning in thoracic diseases; however, it is limited by radiation dose and hardware costs. We present the Transformer Volumetric Super-Resolution Network (\textbf{TVSRN-V2}), a transformer-based super-resolution (SR) framework designed for practical deployment in clinical lung CT analysis. Built from scalable components, including Through-Plane Attention Blocks (TAB) and Swin Transformer V2 -- our model effectively reconstructs fine anatomical details in low-dose CT volumes and integrates seamlessly with downstream analysis pipelines. We evaluate its effectiveness on three critical lung cancer tasks -- lobe segmentation, radiomics, and prognosis -- across multiple clinical cohorts. To enhance robustness across variable acquisition protocols, we introduce pseudo-low-resolution augmentation, simulating scanner diversity without requiring private data. TVSRN-V2 demonstrates a significant improvement in segmentation accuracy (+4\% Dice), higher radiomic feature reproducibility, and enhanced predictive performance (+0.06 C-index and AUC). These results indicate that SR-driven recovery of structural detail significantly enhances clinical decision support, positioning TVSRN-V2 as a well-engineered, clinically viable system for dose-efficient imaging and quantitative analysis in real-world CT workflows.

Accurate segmentation of pheochromocytoma (PCC) in abdominal CT scans is essential for tumor burden estimation, prognosis, and treatment planning. It may also help infer genetic clusters, reducing reliance on expensive testing. This study systematically evaluates anatomical priors to identify configurations that improve deep learning-based PCC segmentation. We employed the nnU-Net framework to evaluate eleven annotation strategies for accurate 3D segmentation of pheochromocytoma, introducing a set of novel multi-class schemes based on organ-specific anatomical priors. These priors were derived from adjacent organs commonly surrounding adrenal tumors (e.g., liver, spleen, kidney, aorta, adrenal gland, and pancreas), and were compared against a broad body-region prior used in previous work. The framework was trained and tested on 105 contrast-enhanced CT scans from 91 patients at the NIH Clinical Center. Performance was measured using Dice Similarity Coefficient (DSC), Normalized Surface Distance (NSD), and instance-wise F1 score. Among all strategies, the Tumor + Kidney + Aorta (TKA) annotation achieved the highest segmentation accuracy, significantly outperforming the previously used Tumor + Body (TB) annotation across DSC (p = 0.0097), NSD (p = 0.0110), and F1 score (25.84% improvement at an IoU threshold of 0.5), measured on a 70-30 train-test split. The TKA model also showed superior tumor burden quantification (R^2 = 0.968) and strong segmentation across all genetic subtypes. In five-fold cross-validation, TKA consistently outperformed TB across IoU thresholds (0.1 to 0.5), reinforcing its robustness and generalizability. These findings highlight the value of incorporating relevant anatomical context in deep learning models to achieve precise PCC segmentation, supporting clinical assessment and longitudinal monitoring.

Medical image segmentation suffers from data scarcity, particularly in polyp detection where annotation requires specialized expertise. We present SynDiff, a framework combining text-guided synthetic data generation with efficient diffusion-based segmentation. Our approach employs latent diffusion models to generate clinically realistic synthetic polyps through text-conditioned inpainting, augmenting limited training data with semantically diverse samples. Unlike traditional diffusion methods requiring iterative denoising, we introduce direct latent estimation enabling single-step inference with T x computational speedup. On CVC-ClinicDB, SynDiff achieves 96.0% Dice and 92.9% IoU while maintaining real-time capability suitable for clinical deployment. The framework demonstrates that controlled synthetic augmentation improves segmentation robustness without distribution shift. SynDiff bridges the gap between data-hungry deep learning models and clinical constraints, offering an efficient solution for deployment in resourcelimited medical settings.

Interpretability is critical in high-stakes domains such as medical imaging, where understanding model decisions is essential for clinical adoption. In this work, we introduce Sparse Autoencoder (SAE)-based interpretability to breast imaging by analyzing {Mammo-CLIP}, a vision--language foundation model pretrained on large-scale mammogram image--report pairs. We train a patch-level \texttt{Mammo-SAE} on Mammo-CLIP to identify and probe latent features associated with clinically relevant breast concepts such as \textit{mass} and \textit{suspicious calcification}. Our findings reveal that top activated class level latent neurons in the SAE latent space often tend to align with ground truth regions, and also uncover several confounding factors influencing the model's decision-making process. Additionally, we analyze which latent neurons the model relies on during downstream finetuning for improving the breast concept prediction. This study highlights the promise of interpretable SAE latent representations in providing deeper insight into the internal workings of foundation models at every layer for breast imaging.

To compare the trueness of artificial intelligence (AI)-based, manual, and global segmentation protocols by superimposing the resulting segmented 3D models onto reference gold standard surface scan models. Twelve dry human mandibles were used. A cone beam computed tomography (CBCT) scanner was used to scan the mandibles, and the acquired digital imaging and communications in medicine (DICOM) files were segmented using three protocols: global thresholding, manual, and AI-based segmentation (Diagnocat; Diagnocat, San Francisco, CA). The segmented files were exported as study 3D models. A structured light surface scanner (GoSCAN Spark; Creaform 3D, Levis, Canada) was used to scan all mandibles, and the resulting reference 3D models were exported. The study 3D models were compared with the respective reference 3D models by using a mesh comparison software (Geomagic Design X; 3D Systems Inc, Rock Hill, SC). Root mean square (RMS) error values were recorded to measure the magnitude of deviation (trueness), and color maps were obtained to visualize the differences. Comparisons of the trueness of three segmentation methods for differences in RMS were made using repeated measures analysis of variance (ANOVA). A two-sided 5% significance level was used for all tests in the software program. AI-based segmentations had significantly higher RMS values than manual segmentations for the entire mandible (p < 0.001), alveolar process (p < 0.001), and body of the mandible (p < 0.001). AI-based segmentations had significantly lower RMS values than manual segmentations for the condyles (p = 0.018) and ramus (p = 0.013). No significant differences were found between the AI-based and manual segmentations for the coronoid process (p = 0.275), symphysis (p = 0.346), and angle of the mandible (p = 0.344). Global thresholding had significantly higher RMS values than manual segmentations for the alveolus (p < 0.001), angle of the mandible (p < 0.001), body of the mandible (p < 0.001), condyles (p < 0.001), coronoid (p = 0.002), entire mandible (p < 0.001), ramus (p < 0.001), and symphysis (p < 0.001). Global thresholding had significantly higher RMS values than AI-based segmentation for the alveolar process (p = 0.002), angle of the mandible (p < 0.001), body of the mandible (p < 0.001), condyles (p < 0.001), coronoid (p = 0.017), mandible (p < 0.001), ramus (p < 0.001), and symphysis (p < 0.001). AI-based segmentations produced lower RMS values, indicating truer 3D models, compared to global thresholding, and showed no significant differences in some areas compared to manual segmentation. Thus, AI-based segmentation offers a level of segmentation trueness acceptable for use as an alternative to manual or global thresholding segmentation protocols.

Spinal navigation systems require pre- and/or intra-operative 3-D imaging, which expose young patients to harmful radiation. We assessed a scoliosis-specific MRI-protocol that provides T2-weighted MRI and AI-generated synthetic-CT (sCT) scans, through deep learning algorithms. This study aims to compare MRI-based synthetic-CT spinal navigation to CT for safety and accuracy of pedicle screw planning and placement at thoracic and lumbar levels. Spines of 5 cadavers were scanned with thin-slice CT and the scoliosis-specific MRI-protocol (to create sCT). Preoperatively, on both CT and sCT screw trajectories were planned. Subsequently, four spine surgeons performed surface-matched, navigated placement of 2.5 mm k-wires in all pedicles from T3 to L5. Randomization for CT/sCT, surgeon and side was performed (1:1 ratio). On postoperative CT-scans, virtual screws were simulated over k-wires. Maximum angulation, distance between planned and postoperative screw positions and medial breach rate (Gertzbein-Robbins classification) were assessed. 140 k-wires were inserted, 3 were excluded. There were no pedicle breaches > 2 mm. Of sCT-guided screws, 59 were grade A and 10 grade B. For the CT-guided screws, 47 were grade A and 21 grade B (p = 0.022). Average distance (± SD) between intraoperative and postoperative screw positions was 2.3 ± 1.5 mm in sCT-guided screws, and 2.4 ± 1.8 mm for CT (p = 0.78), average maximum angulation (± SD) was 3.8 ± 2.5° for sCT and 3.9 ± 2.9° for CT (p = 0.75). MRI-based, AI-generated synthetic-CT spinal navigation allows for safe and accurate planning and placement of thoracic and lumbar pedicle screws in a cadaveric model, without significant differences in distance and angulation between planned and postoperative screw positions compared to CT.

PXseg, a novel approach for tooth segmentation, numbering and abnormal morphology detection in panoramic X-ray (PX), was designed and promoted through optimizing annotation and applying pre-training. Derived from multicenter, ctPXs generated from cone beam computed tomography (CBCT) with accurate 3D labels were utilized for pre-training, while conventional PXs (cPXs) with 2D labels were input for training. Visual and statistical analyses were conducted using the internal dataset to assess segmentation and numbering performances of PXseg and compared with the model without ctPX pre-training, while the accuracy of PXseg detecting abnormal teeth was evaluated using the external dataset consisting of cPXs with complex dental diseases. Besides, a diagnostic testing was performed to contrast diagnostic efficiency with and without PXseg's assistance. The DSC and F1-score of PXseg in tooth segmentation reached 0.882 and 0.902, which increased by 4.6% and 4.0% compared to the model without pre-training. For tooth numbering, the F1-score of PXseg reached 0.943 and increased by 2.2%. Based on the promotion in segmentation, the accuracy of abnormal tooth morphology detection exceeded 0.957 and was 4.3% higher. A website was constructed to assist in PX interpretation, and the diagnostic efficiency was greatly enhanced with the assistance of PXseg. The application of accurate labels in ctPX increased the pre-training weight of PXseg and improved the training effect, achieving promotions in tooth segmentation, numbering and abnormal morphology detection. Rapid and accurate results provided by PXseg streamlined the workflow of PX diagnosis, possessing significant clinical application prospect.