Computer aided diagnosis system using dermatoscopical image

Computer Aided Diagnosis (CAD) systems for melanoma detection aim to mirror the expert dermatologist decision when watching a dermoscopic or clinical image. Computer Vision techniques, which can be based on expert knowledge or not, are used to characterize the lesion image. This information is delivered to a machine learning algorithm, which gives a diagnosis suggestion as an output. This research is included into this field, and addresses the objective of implementing a complete CAD system using ‘state of the art’ descriptors and dermoscopy images as input. Some of them are based on expert knowledge and others are typical in a wide variety of problems. Images are initially transformed into oRGB, a perceptual color space, looking for both enhancing the information that images provide and giving human perception to machine algorithms. Feature selection is also performed to find features that really contribute to discriminate between benign and malignant pigmented skin lesions (PSL). The problem of robust model fitting versus statistically significant system evaluation is critical when working with small datasets, which is indeed the case. This topic is not generally considered in works related to PSLs. Consequently, a method that optimizes the compromise between these two goals is proposed, giving non-overfitted models and statistically significant measures of performance. In this manner, different systems can be compared in a fairer way. A database which enjoys wide international acceptance among dermatologists is used for the experiments.Ingeniería de Sistemas Audiovisuale

Diagnosis of Skin Lesions Based on Dermoscopic Images Using Image Processing Techniques

Great effort has been put into the development of diagnosis methods for the most dangerous type of skin diseases—melanoma. This paper aims to develop a prototype capable of segment and classify skin lesions in dermoscopy images based on ABCD rule. The proposed work is divided into four distinct stages: (1) pre-processing, consists of filtering and contrast enhancing techniques, (2) segmentation, thresholding, and statistical properties are computed to localize the lesion, (3) features extraction, asymmetry is calculated by averaging the calculated results of the two methods: entropy and bi-fold. Border irregularity is calculated by accumulate the statistical scores of the eight segments of the segmented lesion. Color feature is calculated among the existence of six candidate colors: white, black, red, light-brown, dark-brown, and blue-gray. Diameter is measured by the conversion operation from the total number of pixels in the greatest diameter into millimeter (mm), and (4) classification, the summation of the four extracted feature scores multiplied by their weights to yield a total dermoscopy score (TDS); hence, the lesion is classified into benign, suspicious, or malignant. The prototype is implemented in MATLAB and the dataset used consists of 200 dermoscopic images from Hospital Pedro Hispano, Matosinhos. The achieved results show an acceptable performance rates, an accuracy 90%, sensitivity 85%, and specificity 92.22%

Lacunarity Analysis: A Promising Method for the Automated Assessment of Melanocytic Naevi and Melanoma

The early diagnosis of melanoma is critical to achieving reduced mortality and increased survival. Although clinical examination is currently the method of choice for melanocytic lesion assessment, there is a growing interest among clinicians regarding the potential diagnostic utility of computerised image analysis. Recognising that there exist significant shortcomings in currently available algorithms, we are motivated to investigate the utility of lacunarity, a simple statistical measure previously used in geology and other fields for the analysis of fractal and multi-scaled images, in the automated assessment of melanocytic naevi and melanoma. Digitised dermoscopic images of 111 benign melanocytic naevi, 99 dysplastic naevi and 102 melanomas were obtained over the period 2003 to 2008, and subject to lacunarity analysis. We found the lacunarity algorithm could accurately distinguish melanoma from benign melanocytic naevi or non-melanoma without introducing many of the limitations associated with other previously reported diagnostic algorithms. Lacunarity analysis suggests an ordering of irregularity in melanocytic lesions, and we suggest the clinical application of this ordering may have utility in the naked-eye dermoscopic diagnosis of early melanoma

Extraction of specific parameters for skin tumour classification

In this paper, a methodological approach to the classification of tumour skin lesions in dermoscopy images is presented. Melanomas are the most malignant skin tumours. They grow in melanocytes, the cells responsible for pigmentation. This type of cancer is increasing rapidly; its related mortality rate is increasing more modestly, and inversely proportional to the thickness of the tumour. The mortality rate can be decreased by earlier detection of suspicious lesions and better prevention. Using skin tumour features such as colour, symmetry and border regularity, an attempt is made to determine if the skin tumour is a melanoma or a benign tumour. In this work, we are interested in extracting specific attributes which can be used for computer-aided diagnosis of melanoma, especially among general practitioners. In the first step, we eliminate surrounding hair in order to eliminate the residual noise. In the second step, an automatic segmentation is applied to the image of the skin tumour. This method reduces a colour image into an intensity image and approximately segments the image by intensity thresholding. Then, it refines the segmentation using the image edges, which are used to localize the boundary in that area of the skin. This step is essential to characterize the shape of the lesion and also to locate the tumour for analysis. Then, a sequences of transformations is applied to the image to measure a set of attributes (A: asymmetry, B: border, C: colour and D: diameter) which contain sufficient information to differentiate a melanoma from benign lesions. Finally, the various signs of specific lesion (ABCD) are provided to an artificial neural network to differentiate between malignant tumours and benign lesions

Stacked Cross Validation with Deep Features: A Hybrid Method for Skin Cancer Detection

Detection of malignant skin lesions is important for early and accurate diagnosis of skin cancer. In this work, a hybrid method for malignant lesion detection from dermoscopy images is proposed. The method combines the feature extraction process of convolutional neural networks (CNN) with an ensemble learner called stacked cross-validation (CV). The features extracted by three different CNN architectures, namely, ResNet50, Xception, and VGG16 are used for training of four different baseline classifiers, which are support vector machines, k-nearest neighbors, artificial neural networks, and random forests. The stacked outputs of these classifiers are used to train a logistic regression model as a meta-classifier. The performance of the proposed method is compared with the baseline classifiers trained individually as well as AdaBoost classifier, another ensemble learner. Feature extraction with Xception architecture, outperforms all other benchmark models by achieving scores of 0.909, 0.896, 0.886, and 0.917 for accuracy, F1-score, sensitivity, and AUC, respectively

Automatic Detection of Critical Dermoscopy Features for Malignant Melanoma Diagnosis

Improved methods for computer-aided analysis of identifying features of skin lesions from digital images of the lesions are provided. Improved preprocessing of the image that 1) eliminates artifacts that occlude or distort skin lesion features and 2) identifies groups of pixels within the skin lesion that represent features and/or facilitate the quantification of features are provided including improved digital hair removal algorithms. Improved methods for analyzing lesion features are also provided

Segmentation and lesion detection in dermoscopic images

This thesis was submitted for the award of Doctor of Philosophy and was awarded by Brunel University LondonMalignant melanoma is one of the most fatal forms of skin cancer. It has also become increasingly common, especially among white-skinned people exposed to the sun. Early detection of melanoma is essential to raise survival rates, since its detection at an early stage can be helpful and curable. Working out the dermoscopic clinical features (pigment network and lesion borders) of melanoma is a vital step for dermatologists, who require an accurate method of reaching the correct clinical diagnosis, and ensure the right area receives the correct treatment. These structures are considered one of the main keys that refer to melanoma or non-melanoma disease. However, determining these clinical features can be a time-consuming, subjective (even for trained clinicians) and challenging task for several reasons: lesions vary considerably in size and colour, low contrast between an affected area and the surrounding healthy skin, especially in early stages, and the presence of several elements such as hair, reflections, oils and air bubbles on almost all images. This thesis aims to provide an accurate, robust and reliable automated dermoscopy image analysis technique, to facilitate the early detection of malignant melanoma disease. In particular, four innovative methods are proposed for region segmentation and classification, including two for pigmented region segmentation, one for pigment network detection, and one for lesion classification. In terms of boundary delineation, four pre-processing operations, including Gabor filter, image sharpening, Sobel filter and image inpainting methods are integrated in the segmentation approach to delete unwanted objects (noise), and enhance the appearance of the lesion boundaries in the image. The lesion border segmentation is performed using two alternative approaches. The Fuzzy C-means and the Markov Random Field approaches detect the lesion boundary by repeating the labeling of pixels in all clusters, as a first method. Whereas, the Particle Swarm Optimization with the Markov Random Field method achieves greater accuracy for the same aim by combining them in the second method to perform a local search and reassign all image pixels to its cluster properly. With respect to the pigment network detection, the aforementioned pre-processing method is applied, in order to remove most of the hair while keeping the image information and increase the visibility of the pigment network structures. Therefore, a Gabor filter with connected component analysis are used to detect the pigment network lines, before several features are extracted and fed to the Artificial Neural Network as a classifier algorithm. In the lesion classification approach, the K-means is applied to the segmented lesion to separate it into homogeneous clusters, where important features are extracted; then, an Artificial Neural Network with Radial Basis Functions is trained by representative features to classify the given lesion as melanoma or not. The strong experimental results of the lesion border segmentation methods including Fuzzy C-means with Markov Random Field and the combination between the Particle Swarm Optimization and Markov Random Field, achieved an average accuracy of 94.00% , 94.74% respectively. Whereas, the lesion classification stage by using extracted features form pigment network structures and segmented lesions achieved an average accuracy of 90.1% , 95.97% respectively. The results for the entire experiment were obtained using a public database PH2 comprising 200 images. The results were then compared with existing methods in the literature, which have demonstrated that our proposed approach is accurate, robust, and efficient in the segmentation of the lesion boundary, in addition to its classification