Background: Pancreatic cystic lesions (PCLs) are frequent and underreported incidental findings on computed tomography (CT) scans and can evolve to pancreatic cancer—the most lethal cancer, with less than 5 months of life expectancy. Objective: The aim of this study was to develop and validate an artificial deep neural network (attention gate U-Net, also named “AGNet”) for automated detection of PCLs. This kind of technology can help radiologists to cope with an increasing demand of cross-sectional imaging tests and increase the number of PCLs incidentally detected, thus increasing the early detection of pancreatic cancer. Methods: We adapted and evaluated an algorithm based on an attention gate U-Net architecture for automated detection of PCL on CTs. A total of 335 abdominal CTs with PCLs and control cases were manually segmented in 3D by 2 radiologists with over 10 years of experience in consensus with a board-certified radiologist specialized in abdominal radiology. This information was used to train a neural network for segmentation followed by a postprocessing pipeline that filtered the results of the network and applied some physical constraints, such as the expected position of the pancreas, to minimize the number of false positives. Results: Of 335 studies included in this study, 297 had a PCL, including serous cystadenoma, intraductal pseudopapillary mucinous neoplasia, mucinous cystic neoplasm, and pseudocysts . The Shannon Index of the chosen data set was 0.991 with an evenness of 0.902. The mean sensitivity obtained in the detection of these lesions was 93.1% (SD 0.1%), and the specificity was 81.8% (SD 0.1%). Conclusions: This study shows a good performance of an automated artificial deep neural network in the detection of PCL on both noncontrast- and contrast-enhanced abdominal CT scans.
Designing optimal and light weight networks to fit in resource-limited platforms like mobiles, DSPs or GPUs is a challenging problem with a wide range of interesting applications, e.g. in embedded systems for autonomous driving. While most approaches are based on manual hyperparameter tuning, there exist a new line of research, the so-called NAS (Neural Architecture Search) methods, that aim to optimize several metrics during the design process, including memory requirements of the network, number of FLOPs, number of MACs (Multiply-ACcumulate operations) or inference latency. However, while NAS methods have shown very promising results, they are still significantly time and cost consuming. In this work we introduce E-DNAS, a differentiable architecture search method, which improves the efficiency of NAS methods in designing light-weight networks for the task of image classification. Concretely, E-DNAS computes, in a differentiable manner, the optimal size of a number of meta-kernels that capture patterns of the input data at different resolutions. We also leverage on the additive property of convolution operations to merge several kernels with different compatible sizes into a single one, reducing thus the number of operations and the time required to estimate the optimal configuration. We evaluate our approach on several datasets to perform classification. We report results in terms of the SoC (System on Chips) metric, typically used in the Texas Instruments TDA2x families for autonomous driving applications. The results show that our approach allows designing low latency architectures significantly faster than state-of-the-art.
In this paper we address the problem of extracting vehicle 3D pose from 2D RGB images. An accurate methodology is presented that is capable of locating 3D coordinates of 20 pre-defined semantic vehicle points of interest or keypoints from 2D information. The presented two-step pipeline provides a straightforward way of extracting three-dimensional information from planar images and avoiding also the usage of other sensor that would lead to a more expensive and hard to manage system. The main contribution of this work is the presented dedicated network architectures that are able to locate simultaneously occluded and visible semantic points of interest to convert these 2D points into 3D space in a simple but efficient way. The presented method uses a robust network based on Stack-Hourglass architecture for precise prediction of semantic 2D keypoints from vehicles even if they are occluded. Furthermore, in the second step another dedicated network converts the 2D points into 3D world coordinates and therefore, the 3D pose of the vehicle can be automatically extracted, outperforming state-of-the-art techniques in terms of accuracy.
The increasing use of high-resolution cross-sectional imaging has significantly enhanced the detection of pancreatic cystic lesions (PCLs), including pseudocysts and neoplastic entities such as IPMN, MCN, and SCN. However, accurate categorization of PCLs remains a challenge. This study aims to improve PCL evaluation by developing and validating a radiomics-based software tool leveraging machine learning (ML) for lesion classification. The model categorizes PCLs into mucinous and non-mucinous types using a custom dataset of 261 CT examinations, with 156 images for training and 105 for external validation. Three experienced radiologists manually delineated the images, extracting 38 radiological and 214 radiomic features using the Pyradiomics module in Python 3.13.2. Feature selection was performed using Least Absolute Shrinkage and Selection Operator (LASSO) regression, followed by classification with an Adaptive Boosting (AdaBoost) model trained on the optimized feature set. The proposed model achieved an accuracy of 89.3% in the internal validation cohort and demonstrated robust performance in the external validation cohort, with 90.2% sensitivity, 80% specificity, and 88.2% overall accuracy. Comparative analysis with existing radiomics-based studies showed that the proposed model either outperforms or performs on par with the current state-of-the-art methods, particularly in external validation scenarios. These findings highlight the potential of radiomics-driven machine learning approaches in enhancing PCL diagnosis across diverse patient populations.
11 September 2025 in Computers in Biology and Medicine