The association between dermoscopic features and BRAF mutational status in cutaneous melanoma: significance of the blue-white veil.
By: M Armengot-Carbó, E Nagore, Z García-Casado, R Botella-Estrada

Department of Dermatology, Hospital General Universitari de Castelló [General University Hospital of Castellon], Castellón de la Plana, Spain; Universidad Cardenal Herrera-CEU [University Cardenal Herrera-CEU], CEU Universities. Electronic address: miquelarmengot@gmail.com.
2017-10-22; doi: 10.1016/j.jaad.2017.12.064
Abstract

Background

The genetic basis of melanoma affects its clinicopathological characteristics and increasingly influences its management. BRAF-mutated melanoma may present with specific dermoscopic features.

Objectives

To identify the dermoscopic features associated with BRAF mutation in cutaneous melanoma and to evaluate a model capable of predicting BRAF mutations based on dermoscopic and clinicopathological features easily accessible in normal clinical practice.

Methods

A prospective, cross-sectional, observational, and descriptive study was performed. Ninety-three cutaneous melanomas with dermoscopic images from 93 patients were included. BRAF mutational status was determined by genetic analysis using two methods: cobas 4800 BRAF V600 Mutation Test and Sanger sequencing. Clinicopathological data were collected; dermoscopic images were analyzed by two independent blind observers.

Results

Blue-white veil in dermoscopy was significantly associated with BRAF mutations (OR: 4.3; 95% CI: 1.6-11.5; p=0.003). Patients with BRAF-mutated melanomas were significantly younger than those with wild-type melanomas (OR: 0.96; 95% CI: 0.93-0.99; p=0.008). Based on these two variables, it was possible to predict BRAF mutational status in melanoma with 73% accuracy.

Limitations

Histological data were obtained from pathology reports. The accuracy of the predictive model has not been tested with a new dataset.

Conclusions

Blue-white veil in dermoscopy is associated with BRAF mutations in cutaneous melanoma.



Copyright © 2018. Published by Elsevier Inc.

PMID:29307636






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