Medical image segmentation is challenging due to overlapping anatomies with ambiguous boundaries and a severe imbalance between the foreground and background classes, which particularly affects the delineation of small lesions. Existing methods, including encoder-decoder networks and prompt-driven variants of the Segment Anything Model (SAM), rely heavily on local cues or user prompts and lack integrated semantic priors, thus failing to generalize well to low-contrast or overlapping targets. To address these issues, we propose MedSeg-R, a lightweight, dual-stage framework inspired by inspired by clinical reasoning. Its cognitive stage interprets medical report into structured semantic priors (location, texture, shape), which are fused via transformer block. In the perceptual stage, these priors modulate the SAM backbone: spatial attention highlights likely lesion regions, dynamic convolution adapts feature filters to expected textures, and deformable sampling refines spatial support. By embedding this fine-grained guidance early, MedSeg-R disentangles inter-class confusion and amplifies minority-class cues, greatly improving sensitivity to small lesions. In challenging benchmarks, MedSeg-R produces large Dice improvements in overlapping and ambiguous structures, demonstrating plug-and-play compatibility with SAM-based systems.

Artificial Intelligence (AI) holds significant promise for improving prognosis prediction in medical imaging, yet its effective application remains challenging. In this work, we introduce a structured benchmark explicitly designed to evaluate and compare the transferability of Convolutional Neural Networks and Foundation Models in predicting clinical outcomes in COVID-19 patients, leveraging diverse publicly available Chest X-ray datasets. Our experimental methodology extensively explores a wide set of fine-tuning strategies, encompassing traditional approaches such as Full Fine-Tuning and Linear Probing, as well as advanced Parameter-Efficient Fine-Tuning methods including Low-Rank Adaptation, BitFit, VeRA, and IA3. The evaluations were conducted across multiple learning paradigms, including both extensive full-data scenarios and more clinically realistic Few-Shot Learning settings, which are critical for modeling rare disease outcomes and rapidly emerging health threats. By implementing a large-scale comparative analysis involving a diverse selection of pretrained models, including general-purpose architectures pretrained on large-scale datasets such as CLIP and DINOv2, to biomedical-specific models like MedCLIP, BioMedCLIP, and PubMedCLIP, we rigorously assess each model's capacity to effectively adapt and generalize to prognosis tasks, particularly under conditions of severe data scarcity and pronounced class imbalance. The benchmark was designed to capture critical conditions common in prognosis tasks, including variations in dataset size and class distribution, providing detailed insights into the strengths and limitations of each fine-tuning strategy. This extensive and structured evaluation aims to inform the practical deployment and adoption of robust, efficient, and generalizable AI-driven solutions in real-world clinical prognosis prediction workflows.

As the deep learning revolution marches on, masked modeling has emerged as a distinctive approach that involves predicting parts of the original data that are proportionally masked during training, and has demonstrated exceptional performance in multiple fields. Magnetic Resonance Imaging (MRI) reconstruction is a critical task in medical imaging that seeks to recover high-quality images from under-sampled k-space data. However, previous MRI reconstruction strategies usually optimized the entire image domain or k-space, without considering the importance of different frequency regions in the k-space This work introduces a diffusion model based on adaptive masks (AMDM), which utilizes the adaptive adjustment of frequency distribution based on k-space data to develop a hybrid masks mechanism that adapts to different k-space inputs. This enables the effective separation of high-frequency and low-frequency components, producing diverse frequency-specific representations. Additionally, the k-space frequency distribution informs the generation of adaptive masks, which, in turn, guide a closed-loop diffusion process. Experimental results verified the ability of this method to learn specific frequency information and thereby improved the quality of MRI reconstruction, providing a flexible framework for optimizing k-space data using masks in the future.

Foundation models for volumetric medical image segmentation have emerged as powerful tools in clinical workflows, enabling radiologists to delineate regions of interest through intuitive clicks. While these models demonstrate promising capabilities in segmenting previously unseen anatomical structures, their performance is strongly influenced by prompt quality. In clinical settings, radiologists often provide suboptimal prompts, which affects segmentation reliability and accuracy. To address this limitation, we present SafeClick, an error-tolerant interactive segmentation approach for medical volumes based on hierarchical expert consensus. SafeClick operates as a plug-and-play module compatible with foundation models including SAM 2 and MedSAM 2. The framework consists of two key components: a collaborative expert layer (CEL) that generates diverse feature representations through specialized transformer modules, and a consensus reasoning layer (CRL) that performs cross-referencing and adaptive integration of these features. This architecture transforms the segmentation process from a prompt-dependent operation to a robust framework capable of producing accurate results despite imperfect user inputs. Extensive experiments across 15 public datasets demonstrate that our plug-and-play approach consistently improves the performance of base foundation models, with particularly significant gains when working with imperfect prompts. The source code is available at https://github.com/yifangao112/SafeClick.

Segmenting biomarkers in medical images is crucial for various biotech applications. Despite advances, Transformer and CNN based methods often struggle with variations in staining and morphology, limiting feature extraction. In medical image segmentation, where datasets often have limited sample availability, recent state-of-the-art (SOTA) methods achieve higher accuracy by leveraging pre-trained encoders, whereas end-to-end methods tend to underperform. This is due to challenges in effectively transferring rich multiscale features from encoders to decoders, as well as limitations in decoder efficiency. To address these issues, we propose an architecture that captures multi-scale local and global contextual information and a novel decoder design, which effectively integrates features from the encoder, emphasizes important channels and regions, and reconstructs spatial dimensions to enhance segmentation accuracy. Our method, compatible with various encoders, outperforms SOTA methods, as demonstrated by experiments on four datasets and ablation studies. Specifically, our method achieves absolute performance gains of 2.76% on MoNuSeg, 3.12% on DSB, 2.87% on Electron Microscopy, and 4.03% on TNBC datasets compared to existing SOTA methods. Code: https://github.com/saadwazir/MCADS-Decoder

Existing foundation models for neuroimaging are often prohibitively large and data-intensive. We introduce BrainSymphony, a lightweight, parameter-efficient foundation model that achieves state-of-the-art performance while being pre-trained on significantly smaller public datasets. BrainSymphony's strong multimodal architecture processes functional MRI data through parallel spatial and temporal transformer streams, which are then efficiently distilled into a unified representation by a Perceiver module. Concurrently, it models structural connectivity from diffusion MRI using a novel signed graph transformer to encode the brain's anatomical structure. These powerful, modality-specific representations are then integrated via an adaptive fusion gate. Despite its compact design, our model consistently outperforms larger models on a diverse range of downstream benchmarks, including classification, prediction, and unsupervised network identification tasks. Furthermore, our model revealed novel insights into brain dynamics using attention maps on a unique external psilocybin neuroimaging dataset (pre- and post-administration). BrainSymphony establishes that architecturally-aware, multimodal models can surpass their larger counterparts, paving the way for more accessible and powerful research in computational neuroscience.

Endoscopic image classification plays a pivotal role in medical diagnostics by identifying anatomical landmarks and pathological findings. However, conventional closed-set classification frameworks are inherently limited in open-world clinical settings, where previously unseen conditions can arise andcompromise model reliability. To address this, we explore the application of Open Set Recognition (OSR) techniques on the Kvasir dataset, a publicly available and diverse endoscopic image collection. In this study, we evaluate and compare the OSR capabilities of several representative deep learning architectures, including ResNet-50, Swin Transformer, and a hybrid ResNet-Transformer model, under both closed-set and open-set conditions. OpenMax is adopted as a baseline OSR method to assess the ability of these models to distinguish known classes from previously unseen categories. This work represents one of the first efforts to apply open set recognition to the Kvasir dataset and provides a foundational benchmark for evaluating OSR performance in medical image analysis. Our results offer practical insights into model behavior in clinically realistic settings and highlight the importance of OSR techniques for the safe deployment of AI systems in endoscopy.

Incidental pulmonary nodules are very frequently found on CT imaging and may represent (early stage) lung cancers without any signs or symptoms. These incidental findings can be solid lesions or ground glass lesions that may be solitary or multiple. Careful, and systematic evaluation of these findings in imaging is needed to determine the risk of malignancy, based on imaging characteristics, patient factors like smoking habits, prior cancers or family history, and growth rate preferably determined by volume measurements. Once the risk of malignancy is increased, minimal invasive image guided biopsy is warranted, preferably by navigation bronchoscopy. We present two cases to illustrate this clinical workup: one case with a benign solitary pulmonary nodule, and a second case with multiple ground glass opacities, diagnosed as synchronous primary adenocarcinomas of the lung. This is followed by a review of the current status of computer and artificial intelligence aided diagnostic support and clinical workflow optimization.

BackgroundManual data curation was necessary to extract radiology reports due to the ambiguities of natural language.PurposeTo develop a fine-tuned large language model that classifies computed tomography (CT)-guided interventional radiology reports into technique categories and to compare its performance with that of the readers.Material and MethodsThis retrospective study included patients who underwent CT-guided interventional radiology between August 2008 and November 2024. Patients were chronologically assigned to the training (n = 1142; 646 men; mean age = 64.1 ± 15.7 years), validation (n = 131; 83 men; mean age = 66.1 ± 16.1 years), and test (n = 332; 196 men; mean age = 66.1 ± 14.8 years) datasets. In establishing a reference standard, reports were manually classified into categories 1 (drainage), 2 (lesion biopsy within fat or soft tissue density tissues), 3 (lung biopsy), and 4 (bone biopsy). The bi-directional encoder representation from the transformers model was fine-tuned with the training dataset, and the model with the best performance in the validation dataset was selected. The performance and required time for classification in the test dataset were compared between the best-performing model and the two readers.ResultsCategories 1/2/3/4 included 309/367/270/196, 30/42/40/19, and 75/124/78/55 patients for the training, validation, and test datasets, respectively. The model demonstrated an accuracy of 0.979 in the test dataset, which was significantly better than that of the readers (0.922-0.940) (<i>P</i> ≤0.012). The model classified reports within a 49.8-53.5-fold shorter time compared to readers.ConclusionThe fine-tuned large language model classified CT-guided interventional radiology reports into four categories demonstrating high accuracy within a remarkably short time.

Pathological complete response (pCR) to neoadjuvant systemic therapy (NAST) is an established prognostic marker in breast cancer (BC). Multimodal deep learning (DL), integrating diverse data sources (radiology, pathology, omics, clinical), holds promise for improving pCR prediction accuracy. This systematic review synthesizes evidence on multimodal DL for pCR prediction and compares its performance against unimodal DL. Following PRISMA, we searched PubMed, Embase, and Web of Science (January 2015-April 2025) for studies applying DL to predict pCR in BC patients receiving NAST, using data from radiology, digital pathology (DP), multi-omics, and/or clinical records, and reporting AUC. Data on study design, DL architectures, and performance (AUC) were extracted. A narrative synthesis was conducted due to heterogeneity. Fifty-one studies, mostly retrospective (90.2%, median cohort 281), were included. Magnetic resonance imaging and DP were common primary modalities. Multimodal approaches were used in 52.9% of studies, often combining imaging with clinical data. Convolutional neural networks were the dominant architecture (88.2%). Longitudinal imaging improved prediction over baseline-only (median AUC 0.91 vs. 0.82). Overall, the median AUC across studies was 0.88, with 35.3% achieving AUC ≥ 0.90. Multimodal models showed a modest but consistent improvement over unimodal approaches (median AUC 0.88 vs. 0.83). Omics and clinical text were rarely primary DL inputs. DL models demonstrate promising accuracy for pCR prediction, especially when integrating multiple modalities and longitudinal imaging. However, significant methodological heterogeneity, reliance on retrospective data, and limited external validation hinder clinical translation. Future research should prioritize prospective validation, integration underutilized data (multi-omics, clinical), and explainable AI to advance DL predictors to the clinical setting.