Unpaired Translation of Chest X-ray Images for Lung Opacity Diagnosis via Adaptive Activation Masks and Cross-Domain Alignment
Junzhi Ning, Dominic Marshall, Yijian Gao, Xiaodan Xing Yang Nan, Yingying Fang, Sheng Zhang, Matthieu Komorowski, Guang Yang
TL;DR
This work tackles the challenge of lung opacity in chest X-rays by proposing an unpaired translation framework that removes opacities while preserving anatomical and radiomic features. It introduces adaptive activation masks (AASPM) to guide selective region modification and a cross-domain alignment module (CDAM) that leverages a frozen pre-trained CXR classifier for feature- and label-level consistency. The method achieves superior translation quality (lower FID and KID) and enhances downstream tasks such as lung border segmentation and lesion classification across RSNA, MIMIC-CXR-ARDS, and JSRT datasets; ablation confirms the contribution of each component. The results suggest practical clinical value by improving visualization, segmentation reliability, and opacity detection, with future plans to reduce artifacts and validate in out-of-distribution settings through prospective studies.
Abstract
Chest X-ray radiographs (CXRs) play a pivotal role in diagnosing and monitoring cardiopulmonary diseases. However, lung opacities in CXRs frequently obscure anatomical structures, impeding clear identification of lung borders and complicating the localization of pathology. This challenge significantly hampers segmentation accuracy and precise lesion identification, which are crucial for diagnosis. To tackle these issues, our study proposes an unpaired CXR translation framework that converts CXRs with lung opacities into counterparts without lung opacities while preserving semantic features. Central to our approach is the use of adaptive activation masks to selectively modify opacity regions in lung CXRs. Cross-domain alignment ensures translated CXRs without opacity issues align with feature maps and prediction labels from a pre-trained CXR lesion classifier, facilitating the interpretability of the translation process. We validate our method using RSNA, MIMIC-CXR-JPG and JSRT datasets, demonstrating superior translation quality through lower Frechet Inception Distance (FID) and Kernel Inception Distance (KID) scores compared to existing methods (FID: 67.18 vs. 210.4, KID: 0.01604 vs. 0.225). Evaluation on RSNA opacity, MIMIC acute respiratory distress syndrome (ARDS) patient CXRs and JSRT CXRs show our method enhances segmentation accuracy of lung borders and improves lesion classification, further underscoring its potential in clinical settings (RSNA: mIoU: 76.58% vs. 62.58%, Sensitivity: 85.58% vs. 77.03%; MIMIC ARDS: mIoU: 86.20% vs. 72.07%, Sensitivity: 92.68% vs. 86.85%; JSRT: mIoU: 91.08% vs. 85.6%, Sensitivity: 97.62% vs. 95.04%). Our approach advances CXR imaging analysis, especially in investigating segmentation impacts through image translation techniques.
