Semantic Segmentation of Pathological Lung Tissue with Dilated Fully Convolutional Networks

Early and accurate diagnosis of interstitial lung diseases (ILDs) is crucial for making treatment decisions, but can be challenging even for experienced radiologists. The diagnostic procedure is based on the detection and recognition of the different ILD pathologies in thoracic CT scans, yet their manifestation often appears similar. In this study, we propose the use of a deep purely convolutional neural network for the semantic segmentation of ILD patterns, as the basic component of a computer aided diagnosis (CAD) system for ILDs. The proposed CNN, which consists of convolutional layers with dilated filters, takes as input a lung CT image of arbitrary size and outputs the corresponding label map. We trained and tested the network on a dataset of 172 sparsely annotated CT scans, within a cross-validation scheme. The training was performed in an end-to-end and semi-supervised fashion, utilizing both labeled and non-labeled image regions. The experimental results show significant performance improvement with respect to the state of the art

Lung Pattern Analysis using Artificial Intelligence for the Diagnosis Support of Interstitial Lung Diseases

Interstitial lung diseases (ILDs) is a group of more than 200 chronic lung disorders characterized by inflammation and scarring of the lung tissue that leads to respiratory failure. Although ILD is a heterogeneous group of histologically distinct diseases, most of them exhibit similar clinical presentations and their diagnosis often presents a diagnostic dilemma. Early diagnosis is crucial for making treatment decisions, while misdiagnosis may lead to life-threatening complications. If a final diagnosis cannot be reached with the high resolution computed tomography scan, additional invasive procedures are required (e.g. bronchoalveolar lavage, surgical biopsy). The aim of this PhD thesis was to investigate the components of a computational system that will assist radiologists with the diagnosis of ILDs, while avoiding the dangerous, expensive and time-consuming invasive biopsies. The appropriate interpretation of the available radiological data combined with clinical/biochemical information can provide a reliable diagnosis, able to improve the diagnostic accuracy of the radiologists. In this thesis, we introduce two convolutional neural networks particularly designed for ILDs and a training scheme that employs knowledge transfer from the similar domain of general texture classification for performance enhancement. Moreover, we investigate the clinical relevance of breathing information for disease classification. The breathing information is quantified as a deformation field between inhale-exhale lung images using a novel 3D convolutional neural network for medical image registration. Finally, we design and evaluate the final end-to-end computational system for ILD classification using lung anatomy segmentation algorithms from the literature and the proposed ILD quantification neural networks. Deep learning approaches have been mostly investigated for all the aforementioned steps, while the results demonstrated their potential in analyzing lung images

Prediction of progression in idiopathic pulmonary fibrosis using CT scans atbaseline: A quantum particle swarm optimization - Random forest approach

Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease characterized by an unpredictable progressive declinein lung function. Natural history of IPF is unknown and the prediction of disease progression at the time ofdiagnosis is notoriously difficult. High resolution computed tomography (HRCT) has been used for the diagnosisof IPF, but not generally for monitoring purpose. The objective of this work is to develop a novel predictivemodel for the radiological progression pattern at voxel-wise level using only baseline HRCT scans. Mainly, thereare two challenges: (a) obtaining a data set of features for region of interest (ROI) on baseline HRCT scans andtheir follow-up status; and (b) simultaneously selecting important features from high-dimensional space, andoptimizing the prediction performance. We resolved the first challenge by implementing a study design andhaving an expert radiologist contour ROIs at baseline scans, depending on its progression status in follow-upvisits. For the second challenge, we integrated the feature selection with prediction by developing an algorithmusing a wrapper method that combines quantum particle swarm optimization to select a small number of featureswith random forest to classify early patterns of progression. We applied our proposed algorithm to analyzeanonymized HRCT images from 50 IPF subjects from a multi-center clinical trial. We showed that it yields aparsimonious model with 81.8% sensitivity, 82.2% specificity and an overall accuracy rate of 82.1% at the ROIlevel. These results are superior to other popular feature selections and classification methods, in that ourmethod produces higher accuracy in prediction of progression and more balanced sensitivity and specificity witha smaller number of selected features. Our work is the first approach to show that it is possible to use onlybaseline HRCT scans to predict progressive ROIs at 6 months to 1year follow-ups using artificial intelligence

Sparse feature learning for image analysis in segmentation, classification, and disease diagnosis.

The success of machine learning algorithms generally depends on intermediate data representation, called features that disentangle the hidden factors of variation in data. Moreover, machine learning models are required to be generalized, in order to reduce the specificity or bias toward the training dataset. Unsupervised feature learning is useful in taking advantage of large amount of unlabeled data, which is available to capture these variations. However, learned features are required to capture variational patterns in data space. In this dissertation, unsupervised feature learning with sparsity is investigated for sparse and local feature extraction with application to lung segmentation, interpretable deep models, and Alzheimer\u27s disease classification. Nonnegative Matrix Factorization, Autoencoder and 3D Convolutional Autoencoder are used as architectures or models for unsupervised feature learning. They are investigated along with nonnegativity, sparsity and part-based representation constraints for generalized and transferable feature extraction

Discriminative Localized Sparse Representations for Breast Cancer Screening

Breast cancer is the most common cancer among women both in developed and developing countries. Early detection and diagnosis of breast cancer may reduce its mortality and improve the quality of life. Computer-aided detection (CADx) and computer-aided diagnosis (CAD) techniques have shown promise for reducing the burden of human expert reading and improve the accuracy and reproducibility of results. Sparse analysis techniques have produced relevant results for representing and recognizing imaging patterns. In this work we propose a method for Label Consistent Spatially Localized Ensemble Sparse Analysis (LC-SLESA). In this work we apply dictionary learning to our block based sparse analysis method to classify breast lesions as benign or malignant. The performance of our method in conjunction with LC-KSVD dictionary learning is evaluated using 10-, 20-, and 30-fold cross validation on the MIAS dataset. Our results indicate that the proposed sparse analyses may be a useful component for breast cancer screening applications

LUNG PATTERN CLASSIFICATION VIA DCNN

Interstitial lung disease (ILD) causes pulmonary fibrosis. The correct classification of ILD plays a crucial role in the diagnosis and treatment process. In this research work, we disclose a lung nodules recognition method based on a deep convolutional neural network (DCNN) and global features, which can be used for computer-aided diagnosis (CAD) of global features of lung nodules. Firstly, a DCNN is constructed based on the characteristics and complexity of lung computerized tomography (CT) images. Then discussed the effects of different iterations on the recognition results and influence of different model structures on the global features of lung nodules. We also improved the convolution kernel size, feature dimension, and network depth. Finally, the effects of different pooling methods, activation functions and training algorithms on the performance of DCNN were analyzed from the network optimization dimension. The experimental results verify the feasibility of the proposed DCNN for CAD of global features of lung nodules. Selecting appropriate model parameters and model structure and using the elastic momentum training method can achieve good recognition results