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Duilio Deangeli

Publications and source records attributed to Duilio Deangeli.

2 recordsLinked to original sources

Abdominal Ultrasound Simulation from Semantic Labels using Paired Label-to-Physics-Based Image Translation

Purpose: Current abdominal ultrasound (US) simulation methods often require CT-based anatomical references for ray-casting, limiting deformation and pathology variability. We propose a learning-based pipeline trained to predict physics-based images derived from CT scans from semantic labels, enabling controlled simulations without patient-specific CT volumes at inference time. Methods: We introduce a two-stage pipeline that maps anatomical segmentations to realistic US images through a simplified US image. Stage~I synthesizes this image from semantic labels using models trained on CT-based ray-casting outputs. Stage~II refines it into a realistic US scan using anatomically guided unpaired translation. Deformations and pathologies are generated by editing anatomical maps. Results: We evaluated Pix2Pix and the Semantic Diffusion Model (SDM) in Stage~I, followed by segmentation-guided CycleGAN (SG-CycleGAN) refinement in Stage~II. SDM significantly outperformed Pix2Pix in morphological metrics, including MAE (19.85 vs. 21.65), SSIM (0.28 vs. 0.24), and mIoU (0.43 vs. 0.29), whereas Pix2Pix yielded better perceptual point estimates (LPIPS: 0.17 vs. 0.19; FID: 0.32 vs. 0.37; KID: 0.25 vs. 0.48). Conclusion: Training paired generative models with physics-based supervision enables approximation of CT-derived ray-casting outputs at inference time directly from semantic labels. Although the pipeline does not require patient-specific CT volumes at inference time, CT-derived segmentations and ray-casting simulations remain necessary to train Stage~I. Once trained, the framework enables controllable healthy and pathological simulations through semantic-map modification.

eess.IV↗

Learning normal asymmetry representations for homologous brain structures

Although normal homologous brain structures are approximately symmetrical by definition, they also have shape differences due to e.g. natural ageing. On the other hand, neurodegenerative conditions induce their own changes in this asymmetry, making them more pronounced or altering their location. Identifying when these alterations are due to a pathological deterioration is still challenging. Current clinical tools rely either on subjective evaluations, basic volume measurements or disease-specific deep learning models. This paper introduces a novel method to learn normal asymmetry patterns in homologous brain structures based on anomaly detection and representation learning. Our framework uses a Siamese architecture to map 3D segmentations of left and right hemispherical sides of a brain structure to a normal asymmetry embedding space, learned using a support vector data description objective. Being trained using healthy samples only, it can quantify deviations-from-normal-asymmetry patterns in unseen samples by measuring the distance of their embeddings to the center of the learned normal space. We demonstrate in public and in-house sets that our method can accurately characterize normal asymmetries and detect pathological alterations due to Alzheimer's disease and hippocampal sclerosis, even though no diseased cases were accessed for training. Our source code is available at https://github.com/duiliod/DeepNORHA.

q-bio.NC↗