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一例转移性 Spitz 样黑色素瘤儿童重度纳武利尤单抗诱导的扁平苔藓样天疱疮。

A case of severe nivolumab-induced lichen planus pemphigoides in a child with metastatic spitzoid melanoma.

机构信息

Department of Dermatology, University of Rochester Medical Center, Rochester, New York, USA.

Department of Pediatrics, University of Rochester Medical Center, Rochester, New York, USA.

出版信息

Pediatr Dermatol. 2023 Jan;40(1):154-156. doi: 10.1111/pde.15097. Epub 2022 Jul 26.

Abstract

Dermatologic reactions are among the most common adverse events of antiprogrammed cell death-1 (anti-PD-1) monoclonal antibodies agents and include maculopapular rash, psoriasiform rash, lichenoid eruptions, autoimmune bullous disorders, and vitiligo. Here, we present a case of a 12-year-old African American male with metastatic spitzoid melanoma treated with nivolumab who developed a mild lichenoid eruption that progressed to a severe case of lichen planus pemphigoides (LPP). Management was complex given the patient's age and history and included hospitalization for intravenous steroids, an intensive topical steroid regimen, methotrexate, and discontinuation of nivolumab. This case illustrates a rare but dramatic progression from a mild LP-like eruption to severe bullous lichenoid eruption, most consistent with LPP, as well as the diagnostic and treatment challenges in the setting of a pediatric patient on nivolumab.

摘要

皮肤反应是抗程序性死亡受体-1(抗 PD-1)单克隆抗体药物最常见的不良反应之一,包括斑丘疹、银屑病样皮疹、苔藓样疹、自身免疫性大疱性疾病和白癜风。在这里,我们报告了一例 12 岁的非洲裔美国男性转移性 Spitz 样黑色素瘤患者,接受 nivolumab 治疗后出现轻度苔藓样疹,进展为严重的扁平苔藓样类天疱疮(LPP)。鉴于患者的年龄和病史,管理非常复杂,包括住院静脉注射类固醇、强化局部类固醇治疗、甲氨蝶呤和停止 nivolumab。本病例说明了从轻度 LP 样疹到严重水疱性苔藓样疹的罕见但戏剧性进展,最符合 LPP,以及在接受 nivolumab 的儿科患者中出现的诊断和治疗挑战。

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