Retinal optical coherence tomography (OCT) imaging is a valuable tool for assessing the condition of the back part of the eye. The condition has a great effect on the specificity of diagnosis, the monitoring of many physiological and pathological procedures, and the response and evaluation of therapeutic effectiveness in various fields of clinical practices, including primary eye diseases and systemic diseases such as diabetes. Therefore, precise diagnosis, classification, and automated image analysis models are crucial. In this paper, we propose an enhanced optical coherence tomography (EOCT) model to classify retinal OCT based on modified ResNet (50) and random forest algorithms, which are used in the proposed study’s training strategy to enhance performance. The Adam optimizer is applied during the training process to increase the efficiency of the ResNet (50) model compared with the common pre-trained models, such as spatial separable convolutions and visual geometry group (VGG) (16). The experimentation results show that the sensitivity, specificity, precision, negative predictive value, false discovery rate, false negative rate accuracy, and Matthew’s correlation coefficient are 0.9836, 0.9615, 0.9740, 0.9756, 0.0385, 0.0260, 0.0164, 0.9747, 0.9788, and 0.9474, respectively.

With the massive success of deep networks, there have been significant efforts to analyze cancer diseases, especially skin cancer. For this purpose, this work investigates the capability of deep networks in diagnosing a variety of dermoscopic lesion images. This paper aims to develop and fine-tune a deep learning architecture to diagnose different skin cancer grades based on dermatoscopic images. Fine-tuning is a powerful method to obtain enhanced classification results by the customized pre-trained network. Regularization, batch normalization, and hyperparameter optimization are performed for fine-tuning the proposed deep network. The proposed fine-tuned ResNet50 model successfully classified 7-respective classes of dermoscopic lesions using the publicly available HAM10000 dataset. The developed deep model was compared against two powerful models, i.e., InceptionV3 and VGG16, using the Dice similarity coefficient (DSC) and the area under the curve (AUC). The evaluation results show that the proposed model achieved higher results than some recent and robust models.

Due to the complexity of skin cancer treatment at later stages, the investigation of an efficient non-invasive automated system can help in guiding diagnosis. This paper proposes a non-invasive automatic system for characterizing malignant melanoma from seborrheic keratosis (BKL) using pixel-based segmentation and feature extraction techniques. The proposed system utilizes the pixel-based features to capture the main characteristics that discriminate BKL and malignant melanoma (MEL). The pixel-based technique enabled single-pixel distributions for color and texture that results in good discrimination of pigmented skin lesions from unaffected skin regions in the processed image. In the experimental results, the obtained characterization result using gradient boosted trees (GBT) is promising and outperformed other state-of-the-art techniques, which had an accuracy equaled to 97.5%, Dice measure equaled to 98.5%, sensitivity equaled to 98.3%, and specificity equaled to 92.1%.

The formation of malignant neoplasm can be seen as deterioration of a pre-malignant skin neoplasm in its functionality and structure. Distinguishing melanocytic skin neoplasms is a challenging task due to their high visual similarity with different types of lesions and the intra-structural variants of melanocytic neoplasms. Besides, there is a high visual likeliness level between different lesion types with inhomogeneous features and fuzzy boundaries. The abnormal growth of melanocytic neoplasms takes various forms from uniform typical pigment network to irregular atypical shape, which can be described by border irregularity of melanocyte lesion image. This work proposes analytical reasoning for the human-observable phenomenon as a high-level feature to determine the neoplasm growth phase using a novel pixel-based feature space. The pixel-based feature space, which is comprised of high-level features and other color and texture features, are fed into the classifier to classify different melanocyte neoplasm phases. The proposed system was evaluated on the PH2 dermoscopic images benchmark dataset. It achieved an average accuracy of 95.1% using a support vector machine (SVM) classifier with the radial basis function (RBF) kernel. Furthermore, it reached an average Disc similarity coefficient (DSC) of 95.1%, an area under the curve (AUC) of 96.9%, and a sensitivity of 99%. The results of the proposed system outperform the results of other state-of-the-art multiclass techniques.