de Lorenzi C, André R, Vuilleumier A, Kaya G, Abosaleh M
Department of Dermatology and Venerealology, Hôpitaux Universitaires de Genève, 4, rue Gabrielle-Perret-Gentil, 1205 Geneva, Switzerland.
Department of Dermatology and Venerealology, Hôpitaux Universitaires de Genève, 4, rue Gabrielle-Perret-Gentil, 1205 Geneva, Switzerland.
Ann Dermatol Venereol. 2020 Mar;147(3):221-227. doi: 10.1016/j.annder.2019.07.008. Epub 2020 Jan 22.
Cutaneous adverse effects of immunotherapies are being seen with increasing frequency in general practice. While anti-PD1 lichenoid reactions are well known, only a few cases of bullous lichen planus have so far been reported in the medical literature. Herein we described a case of secondary bullous lichen planus associated with nivolumab and we present a systematic review of all anti-P1-induced cases reported in the literature.
Three months after beginning treatment with nivolumab for metastatic clear-cell renal carcinoma, a 68-year-old man presented pruritic purplish papules on his limbs that subsequently became bullous. Clinical-histological correlation led us to a diagnosis of secondary bullous lichen planus induced by nivolumab. Systemic steroids and withdrawal of immunotherapy resulted in clinical improvement.
Our systematic review revealed 20 cases of lichen planus induced by anti-PD1 (nivolumab and pembrolizumab) published between 2016 and 2018, 6 of which were of the bullous form. Treatment and maintenance or discontinuation of anti-PD1 were dependent on severity.
Bullous lichen planus has been reported only rarely in the context of nivolumab therapy. The timeline for development of cutaneous adverse reactions under anti-PD1 immunotherapy may last weeks or months and regular monitoring is required. Withdrawal of immunotherapy should only be considered where the outcome under systemic corticosteroids is unfavourable.
免疫疗法的皮肤不良反应在普通临床实践中越来越常见。虽然抗程序性死亡蛋白1(PD1)苔藓样反应已为人熟知,但迄今为止,医学文献中仅报道了少数几例大疱性扁平苔藓病例。在此,我们描述了一例与纳武单抗相关的继发性大疱性扁平苔藓病例,并对文献中报道的所有抗PD1诱导病例进行了系统综述。
一名68岁男性因转移性透明细胞肾癌开始使用纳武单抗治疗3个月后,四肢出现瘙痒性紫色丘疹,随后发展为水疱。临床与组织学相关性诊断为纳武单抗诱导的继发性大疱性扁平苔藓。全身使用类固醇并停用免疫疗法后临床症状改善。
我们的系统综述发现,2016年至2018年间发表了20例由抗PD1(纳武单抗和派姆单抗)诱导的扁平苔藓病例,其中6例为大疱型。抗PD1的治疗及维持或停药取决于严重程度。
在纳武单抗治疗背景下,大疱性扁平苔藓报道较少。抗PD1免疫疗法下皮肤不良反应的发生时间可能持续数周或数月,需要定期监测。只有在全身使用皮质类固醇效果不佳时才考虑停用免疫疗法。