arXiv subjects

Theresa Urban

Publications and source records attributed to Theresa Urban.

6 recordsLinked to original sources

arXiv2026

LoRCA: LoRA Cycle Adaptation for Histology to HiP-CT Translation with DINOv3

Hierarchical Phase-Contrast Tomography (HiP-CT) is a synchrotron based X-ray imaging technique that enables non-destructive, volumetric imaging of intact organs with multi-resolutions bridging 20 $μm$/voxel for whole organs to near-cellular resolution ($\sim$0.8 $μm$/voxel) in local regions. This offers the opportunity to bring volumetric whole-organ context to histology. However, nonlinear registration between H\&E histology and HiP-CT volumes is challenging due to the differences in feature representations of different colour spaces. Synthesis-before-registration methods have shown strong results in histology-to-MRI and histology-to-CT alignment. However, existing approaches either rely on manual anatomical contours or are trained from scratch without semantic constraints, limiting their generalisability to soft tissue organs and novel modalities. We propose LoRCA (LoRA Cycle Adaptation), a cycle consistent style translation framework built on a shared frozen DINOv3 with modality-specific LoRA adapters, learning modality-specific representations that are decoded and adversarially trained. LoRCA enables structure-preserving translation without requiring paired training data. The frozen backbone is intended to be a structural anchor that prevents content drift by preserving pretrained semantic-extraction capability. We evaluate translation quality using Fréchet Inception Distance (FID) and structural fidelity via mutual information and Canny edge preservation. LoRCA outperforms CycleGAN in both translation quality and structural consistency. As a preliminary indicator of downstream registration utility, we find that style-translated images yield increased feature correspondences under MatchAnything on manually aligned HiP-CT and histology test pairs, suggesting that LoRCA-style translation is a promising step towards 2D histological sections to 3D HiP-CT volumes registration.

eess.IV↗

arXiv2026

Fast Eikonal Phase Retrieval for High-Throughput Beamlines

We introduce a fast Eikonal Phase Retrieval (EPR) formulation that accelerates eikonal phase retrieval by more than two orders of magnitude while retaining controlled accuracy. The method is derived from a second-order asymptotic expansion in the propagation distance $L$ and complemented by the leading Wentzel--Kramers--Brillouin (WKB) wave-optics correction, yielding an efficient iterative correction scheme preconditioned by FFT-diagonal, energy-dependent inverse operators (Paganin-type filters). To ensure robustness across practical experimental regimes, we combine two complementary solvers: (i) a local $O(L^2)$ closure that is accurate when eikonal shifts remain sub-pixel, and (ii) a non-local formulation for multi-pixel shifts, in which intensity is propagated through an explicit eikonal ray mapping using a mass-conserving bilinear redisribution on the detector grid, and detector residuals are transferred back to the object grid by the corresponding adjoint (transpose), implemented as bilinear interpolation, before applying an approximate FFT-diagonal preconditioner to accelerate convergence. The same framework supports polychromatic data through a compact spectral discretisation, allowing energy-dependent transport and inversion while keeping the iteration GPU/FFT efficient. Overall, this unified approach enables accurate and computationally efficient phase retrieval across propagation conditions relevant to high-throughput PPC-$μ$CT experiments.

physics.optics↗

arXiv2025

Look-Up Table-Correction for Beam Hardening-Induced Signal of Clinical Dark-Field Chest Radiographs

Background: Material structures at the micrometer scale cause ultra-small-angle X-ray scattering, e.g., seen in lung tissue or plastic foams. In grating-based X-ray imaging, this causes a reduction of the fringe visibility, forming a dark-field signal. Polychromatic beam hardening also changes visibility, adding a false dark-field signal due to attenuation, even in homogeneous, non-scattering materials. Purpose: The objective of this study is to develop a fast, simple, and robust method to correct dark-field signals and bony structures present due to beam hardening on dark-field chest radiographs of study participants. Methods: The method is based on calibration measurements and image processing. Beam hardening by bones and soft tissue is modeled by aluminum and water, respectively, which have no microstructure and thus only generate an artificial dark-field signal. Look-up tables were then created for both. By using a weighted mean of these, forming a single look-up table, and using the attenuation images, the artificial dark-field signal and thus the bone structures present are reduced for study participants. Results: It was found that applying a correction using a weighted look-up table leads to a significant reduction of bone structures in the dark-field image. The weighting of the aluminum component has a substantial impact on the degree to which bone structures remain visible in the dark-field image. Furthermore, a large negative bias in the dark-field image, dependent on the aluminum weighting, was successfully corrected. Conclusions: The beam-hardening-induced signal in the dark-field images was successfully reduced using the method described. The choice of aluminum weighting to suppress rib structures, as well as the selection of bias correction, should be evaluated based on the specific clinical question.

physics.med-ph↗

arXiv2024

Optimizing Convolutional Neural Networks for Chronic Obstructive Pulmonary Disease Detection in Clinical Computed Tomography Imaging

We aim to optimize the binary detection of Chronic Obstructive Pulmonary Disease (COPD) based on emphysema presence in the lung with convolutional neural networks (CNN) by exploring manually adjusted versus automated window-setting optimization (WSO) on computed tomography (CT) images. 7,194 CT images (3,597 with COPD; 3,597 healthy controls) from 78 subjects were selected retrospectively (10.2018-12.2021) and preprocessed. For each image, intensity values were manually clipped to the emphysema window setting and a baseline 'full-range' window setting. Class-balanced train, validation, and test sets contained 3,392, 1,114, and 2,688 images. The network backbone was optimized by comparing various CNN architectures. Furthermore, automated WSO was implemented by adding a customized layer to the model. The image-level area under the Receiver Operating Characteristics curve (AUC) [lower, upper limit 95% confidence] was utilized to compare model variations. Repeated inference (n=7) on the test set showed that the DenseNet was the most efficient backbone and achieved a mean AUC of 0.80 [0.76, 0.85] without WSO. Comparably, with input images manually adjusted to the emphysema window, the DenseNet model predicted COPD with a mean AUC of 0.86 [0.82, 0.89]. By adding a customized WSO layer to the DenseNet, an optimal window in the proximity of the emphysema window setting was learned automatically, and a mean AUC of 0.82 [0.78, 0.86] was achieved. Detection of COPD with DenseNet models was improved by WSO of CT data to the emphysema window setting range.

eess.IV↗

arXiv2024

Influence of Medical Foreign Bodies on Dark-Field Chest Radiographs: First experiences

Objectives: Evaluating the effects and artifacts introduced by medical foreign bodies in clinical dark-field chest radiographs and assessing their influence on the evaluation of pulmonary tissue, compared to conventional radiographs. Material & Methods: This retrospective study analyzed data from subjects enrolled in clinical trials conducted between 2018 and 2021, focusing on chronic obstructive pulmonary disease (COPD) and COVID-19 patients. All patients obtained a radiograph using an in-house developed clinical prototype for grating-based dark-field chest radiography. The prototype simultaneously delivers a conventional and dark-field radiograph. Two radiologists independently assessed the clinical studies to identify patients with foreign bodies. Subsequently, an analysis was conducted on the effects and artifacts attributed to distinct foreign bodies and their impact on the assessment of pulmonary tissue. Results: Overall, 30 subjects with foreign bodies were included in this study (mean age, 64 years +/- 11 [standard deviation]; 15 men). Foreign bodies composed of materials lacking microstructure exhibited a diminished dark-field signal or no discernible signal. Foreign bodies with a microstructure, in our investigations the cementation of the kyphoplasty, produce a positive dark-field signal. Since most foreign bodies lack microstructural features, dark-field imaging revealed fewer signals and artifacts by foreign bodies compared to conventional radiographs. Conclusion: Dark-field radiography enhances the assessment of pulmonary tissue with overlaying foreign bodies compared to conventional radiography. Reduced interfering signals result in fewer overlapping radiopaque artifacts within the investigated regions. This mitigates the impact on image quality and interpretability of the radiographs and the projection-related limitations of radiography compared to CT.

physics.med-ph↗

arXiv2023

X-ray dark-field signal reduction due to hardening of the visibility spectrum

X-ray dark-field imaging enables a spatially-resolved visualization of ultra-small-angle X-ray scattering. Using phantom measurements, we demonstrate that a material's effective dark-field signal may be reduced by modification of the visibility spectrum by other dark-field-active objects in the beam. This is the dark-field equivalent of conventional beam-hardening, and is distinct from related, known effects, where the dark-field signal is modified by attenuation or phase shifts. We present a theoretical model for this group of effects and verify it by comparison to the measurements. These findings have significant implications for the interpretation of dark-field signal strength in polychromatic measurements.

physics.med-ph↗