Anomaly detection (AD) is the identification of data samples that do not fit a learned data distribution. As such, AD systems can help physicians to determine the presence, severity, and extension of a pathology. Deep generative models, such as Generative Adversarial Networks (GANs), can be exploited to capture anatomical variability. Consequently, any outlier (i.e., sample falling outside of the learned distribution) can be detected as an abnormality in an unsupervised fashion. By using this method, we can not only detect expected or known lesions, but we can even unveil previously unrecognized biomarkers. To the best of our knowledge, this study exemplifies the first AD approach that can efficiently handle volumetric data and detect 3D brain anomalies in one single model. Our proposal is a volumetric and high-detail extension of the 2D f-AnoGAN model obtained by combining a state-of-the-art 3D GAN with refinement training steps. In experiments using non-contrast computed tomography images from traumatic brain injury (TBI) patients, the model detects and localizes TBI abnormalities with an area under the ROC curve of ~75%. Moreover, we test the potential of the method for detecting other anomalies such as low quality images, preprocessing inaccuracies, artifacts, and even the presence of post-operative signs (such as a craniectomy or a brain shunt). The method has potential for rapidly labeling abnormalities in massive imaging datasets, as well as identifying new biomarkers.
翻译:异常检测( AD) 是指识别数据样本, 并不符合所学的数据分布。 因此, AD 系统可以帮助医生确定病理学的存在、 严重程度和扩展范围。 深度基因模型, 如基因反versarial 网络( GANs), 可以用来捕捉解剖变异性。 因此, 任何异常模型( 位于所学分布范围之外的样本) 都可以在不受监督的情况下被检测为异常。 使用这种方法, 我们不仅可以检测预期或已知的损伤, 而且我们甚至可以揭开先前未被承认的生物标志。 根据我们最先进的知识, 这项研究展示了第一个能有效处理体积数据并用单一模型探测3D- AnoGAN 的异常模型。 因此, 我们的建议是一个2D f- AnoGAN 模型的体积和高度分解扩展, 通过将3D GAN 状态的样本与精细的培训步骤相结合, 任何异常的GAN 。 在实验中, 我们不仅可以解析大脑创伤患者( TTII) 的骨质图像( ), 也通过模型检测模型和本地的稳定性 方法,, 也能够检测到 。