Abstract

Dark skin-type individuals have a greater tendency to have pigmentary disorders, among which melasma is especially refractory to treat and often recurs. Objective measurement of melanin amount helps evaluate the treatment response of pigmentary disorders. However, naked-eye evaluation is subjective to weariness and bias. We used a cellular resolution full-field optical coherence tomography (FF-OCT) to assess melanin features of melasma lesions and perilesional skin on the cheeks of eight Asian patients. A computer-aided detection (CADe) system is proposed to mark and quantify melanin. This system combines spatial compounding-based denoising convolutional neural networks (SC-DnCNN), and through image processing techniques, various types of melanin features, including area, distribution, intensity, and shape, can be extracted. Through evaluations of the image differences between the lesion and perilesional skin, a distribution-based feature of confetti melanin without layering, two distribution-based features of confetti melanin in stratum spinosum, and a distribution-based feature of grain melanin at the dermal–epidermal junction, statistically significant findings were achieved (p-values = 0.0402, 0.0032, 0.0312, and 0.0426, respectively). FF-OCT enables the real-time observation of melanin features, and the CADe system with SC-DnCNN was a precise and objective tool with which to interpret the area, distribution, intensity, and shape of melanin on FF-OCT images.

Highlights

  • Dark skin-type individuals have more hyperactive melanocytes compared to the fair skin-type individuals and are prone to develop melasma and other pigmentary disorders [1,2,3]

  • The deposit of melanin in keratinocytes is readily seen on hematoxylin and eosin stain (H&E stain), while melanocytes must be identified by special staining

  • These experiments verified the performance of the computeraided detection (CADe) system and Spatial compounding (SC)-denoising convolutional neural network (DnCNN)

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Summary

Introduction

Dark skin-type individuals have more hyperactive melanocytes compared to the fair skin-type individuals and are prone to develop melasma and other pigmentary disorders [1,2,3]. With the emerging non-invasive techniques, melanin in the epidermis can be visualized because of its brightness by dermatofluoroscopy [4], reflectance confocal microscopy (RCM) [3], multiphoton microscopy [5], and optical coherence tomography (OCT) [6]. Studies suggested melanocytes rapidly transfer the produced melanin to keratinocytes rather than accumulating it [7]. We recently demonstrated the cellular resolution full-field optical coherence tomography (FF-OCT) system allows real-time, non-invasive imaging of superficial skin diseases [6]. These imaging techniques allow observation of in vivo melanolysis and qualitative pigmentary changes, studies with quantitative measurements of the amount and intensity of melanin remain scarce [4,12,13].

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