Pattern recognition in macroscopic and dermoscopic images is a challenging task in skin lesion diagnosis. The search for better performing classification has been a relevant issue for pattern recognition in images. Hence, this work was particularly focused on skin lesion pattern recognition, especially in macroscopic and dermoscopic images. For the pattern recognition in macroscopic images, a computational approach was developed to detect skin lesion features according to the asymmetry, border, colour and texture properties, as well as to diagnose types of skin lesions, i.e., nevus, seborrheic keratosis and melanoma. In this approach, an anisotropic diffusion filter is applied to enhance the input image and an active contour model without edges is used in the segmentation of the enhanced image. Finally , a support vector machine is used to classify each feature property according to their clinical principles, and also for the classification between different types of skin lesions. For the pattern recognition in dermoscopic images, classification models based on ensemble methods and input feature manipulation are used. The feature subsets was used to manipulate the input feature and to ensure the diversity of the ensemble models. Each ensemble classification model was generated by using an optimum-path forest classifier and integrated with a majority voting strategy. The performed experiments allowed to analyse the effectiveness of the developed approaches for pattern recognition in macroscopic and dermoscopic images, with the results obtained being very promising.
Abstract. This paper presents a novel approach to analysis and classification of skin lesions based on their growth pattern. Our method constructs a tree structure for every lesion by repeatedly subdividing the image into sub-images using color based clustering. In this method, segmentation which is a challenging task is not required. The obtained multi-scale tree structure provides a framework that allows us to extract a variety of features, based on the appearance of the tree structure or sub-images corresponding to nodes of the tree. Preliminary features (the number of nodes, leaves, and depth of the tree, and 9 compactness indices of the dark spots represented by the sub-images associated with each node of the tree) are used to train a supervised learning algorithm. Results show the strength of the method in classifying lesions into malignant and benign classes. We achieved Precision of 0.855, Recall of 0.849, and F-measure of 0.834 using 3-layer perceptron and Precision of 0.829, Recall of 0.832, and F-measure of 0.817 using AdaBoost on a dataset containing 112 malignant and 298 benign lesion dermoscopic images.
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