Unit of Dermatology, University of Padua, Padua, Italy.
Unit of Dermatology, University of Padua, Padua, Italy
In Vivo. 2020 Jan-Feb;34(1):441-445. doi: 10.21873/invivo.11793.
A 59-year-old woman, undergoing treatment with encorafenib for metastatic BRAF mutated colorectal cancer, developed during the first two months of therapy multiple eruptive nevi and changes in pre-existing nevi. Development of eruptive nevi has increasingly been reported in association with medications, most frequently conventional immunosuppressants and biologics. Some drugs are associated with eruptive nevi through an indirect effect of their mechanism of action, whereas other drugs are directly implicated in melanocyte proliferation. In this regard, BRAF inhibitors have been demonstrated to activate the MAPK pathway, and to promote cellular proliferation and survival, therefore leading to the development of new melanocytic nevi and to an increase in the size and hyperpigmentation of pre-existing nevi. A dermatological assessment and follow-up should be recommended in all patients presenting with eruptive nevi, regardless of the pathogenesis, because a high number of acquired melanocytic nevi may represent an adjunctive risk factor for melanoma.
一位 59 岁女性因转移性 BRAF 突变结直肠癌接受 encorafenib 治疗,在治疗的头两个月内,她出现了多发性爆发性痣和先前存在的痣的变化。越来越多的药物与爆发性痣有关,最常见的是传统免疫抑制剂和生物制剂。一些药物通过其作用机制的间接作用与爆发性痣有关,而其他药物则直接涉及黑素细胞增殖。在这方面,BRAF 抑制剂已被证明可激活 MAPK 途径,并促进细胞增殖和存活,从而导致新的黑素细胞痣的发展,并增加先前存在的痣的大小和色素沉着。无论发病机制如何,建议所有出现爆发性痣的患者进行皮肤科评估和随访,因为大量获得性黑素细胞痣可能是黑色素瘤的附加危险因素。