白癜风
无容量
色素减退
医学
皮肤病科
黑色素瘤
免疫系统
肿瘤科
免疫学
免疫疗法
癌症研究
作者
Renat Ahatov,Allison Good,Lindy Ross
出处
期刊:Skin
[National Society for Cutaneous Medicine]
日期:2022-01-17
卷期号:6 (1): 65-68
摘要
Vitiligo, manifested by skin hypopigmentation, is an autoimmune disorder of the skin due to the autoimmune destruction of melanocytes. Nivolumab, which is a programmed cell death–1 receptor inhibitor, is a well-known therapy for melanoma. Nivolumab-induced vitiligo has been described in literature, explained by destruction of non-cancerous melanocytes. This is considered a favorable response, due to a correlated stronger immune response against tumor cells. The average onset of the vitiligo is reported to be 5.2 months after starting the therapy, with a maximum reported onset being 9 months. We present a 52-year-old male patient whose initial vitiligo presentation occurred a year after starting the therapy and has continued for months after concluding Nivolumab therapy.
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