Abstract

Melanoma recognition is challenging due to data imbalance and high intra-class variations and large inter-class similarity. Aiming at the issues, we propose a melanoma recognition method using deep convolutional neural network with covariance discriminant loss in dermoscopy images. Deep convolutional neural network is trained under the joint supervision of cross entropy loss and covariance discriminant loss, rectifying the model outputs and the extracted features simultaneously. Specifically, we design an embedding loss, namely covariance discriminant loss, which takes the first and second distance into account simultaneously for providing more constraints. By constraining the distance between hard samples and minority class center, the deep features of melanoma and non-melanoma can be separated effectively. To mine the hard samples, we also design the corresponding algorithm. Further, we analyze the relationship between the proposed loss and other losses. On the International Symposium on Biomedical Imaging (ISBI) 2018 Skin Lesion Analysis dataset, the two schemes in the proposed method can yield a sensitivity of 0.942 and 0.917, respectively. The comprehensive results have demonstrated the efficacy of the designed embedding loss and the proposed methodology.

Highlights

  • Melanoma is the most-deadly type of skin cancer [1]

  • The are summarized as follows: contributions of our work are summarized as follows: (1) We propose a melanoma recognition approach with covariance discriminant (CovD) loss and deepdeep convolutional neural networks (DCNNs), ensuring feature representation and classification ability for melanoma and nonmelanoma

  • Five metrics are adopted for quantitative performance evaluation, including the sensitivity, specificity, accuracy, Receiver Operating Characteristics (ROC) curve, and Area Under the ROC Curve (AUC)

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Summary

Introduction

Melanoma is the most-deadly type of skin cancer [1]. early screening of melanoma benefits the successful treatment, and the estimated 5-year survival rate is over 99% [2]. The manual inspection for dermoscopy images is subjective and experimental. Numerous computer-aided diagnosis methods have been presented to perform melanoma recognition [2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19]. Melanoma recognition is quite challenging owing to the following factors. The performance of melanoma recognition suffers from the data imbalance. In the current public skin lesion datasets, the number of melanoma samples is much smaller than that of the non-melanoma lesions owing to the incidence rate of melanoma. The imbalanced data distribution makes the model biased towards the non-melanoma lesions during the learning process, leading to the missing

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