Pardis Afshar | Searcharxiv

arXiv2026

Infrared Imaging Empowered by Artificial Intelligence for Pediatric Skeletal Triage: A Narrative Review and Future Perspectives

Background. Pediatric musculoskeletal trauma represents up to 18% of pediatric ED visits, yet diagnosis still depends on ionizing radiography. Cumulative low-dose radiation in early life raises lifetime leukemia and brain malignancy risk, motivating radiation-free triage alternatives. Objective. To synthesize evidence for a hybrid framework coupling broad-spectrum infrared (IR) imaging with deep-learning cross-modal translation to generate clinically interpretable synthetic-radiograph reconstructions from non-ionizing data. Approach. We review five IR spectral windows spanning 650 nm to 1 mm - NIR-I, NIR-II, SWIR, MIR/LWIR, and THz - and how dual-geometry (transmission/reflection) acquisition exploits wavelength-specific tissue depth and biochemical sensitivity. We summarize image-to-image translation networks (Pix2Pix, CycleGAN, Swin-Unet) and feature-matching algorithms (SuperPoint, SuperGlue, ALIKED, LightGlue) used to align and fuse IR data into radiograph-equivalent reconstructions. Implications. Pediatric anatomy - smaller cross-sections, thinner cortical bone - favors IR penetration, enabling compact, portable, non-ionizing triage hardware. Feasibility is grounded in fNIRS and transcranial photobiomodulation evidence: near-infrared light passes through skin, skull, and cortex with sufficient signal for hemodynamic monitoring - a longer, more attenuating path than through a pediatric forearm or distal leg. Key barriers: paired IR/X-ray dataset construction, AI-as-medical-device regulatory pathways, generalization across body habitus and skin pigmentation, and acquisition-protocol standardization. Conclusions. Integrated multi-spectral IR+AI imaging is a promising radiation-free complement to pediatric skeletal radiography. Progress requires multi-center paired datasets, externally validated models, and IR source safety qualification under IEC 60825-1.

cs.CV↗

arXiv2024

IBO: Inpainting-Based Occlusion to Enhance Explainable Artificial Intelligence Evaluation in Histopathology

Histopathological image analysis is crucial for accurate cancer diagnosis and treatment planning. While deep learning models, especially convolutional neural networks, have advanced this field, their "black-box" nature raises concerns about interpretability and trustworthiness. Explainable Artificial Intelligence (XAI) techniques aim to address these concerns, but evaluating their effectiveness remains challenging. A significant issue with current occlusion-based XAI methods is that they often generate Out-of-Distribution (OoD) samples, leading to inaccurate evaluations. In this paper, we introduce Inpainting-Based Occlusion (IBO), a novel occlusion strategy that utilizes a Denoising Diffusion Probabilistic Model to inpaint occluded regions in histopathological images. By replacing cancerous areas with realistic, non-cancerous tissue, IBO minimizes OoD artifacts and preserves data integrity. We evaluate our method on the CAMELYON16 dataset through two phases: first, by assessing perceptual similarity using the Learned Perceptual Image Patch Similarity (LPIPS) metric, and second, by quantifying the impact on model predictions through Area Under the Curve (AUC) analysis. Our results demonstrate that IBO significantly improves perceptual fidelity, achieving nearly twice the improvement in LPIPS scores compared to the best existing occlusion strategy. Additionally, IBO increased the precision of XAI performance prediction from 42% to 71% compared to traditional methods. These results demonstrate IBO's potential to provide more reliable evaluations of XAI techniques, benefiting histopathology and other applications. The source code for this study is available at https://github.com/a-fsh-r/IBO.

cs.CV↗