Yamashita Aya, Akasaka Eijiro, Nakano Hajime, Sawamura Daisuke
Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Case Rep Dermatol. 2021 Oct 8;13(3):487-491. doi: 10.1159/000519486. eCollection 2021 Sep-Dec.
A 67-year-old man with non-small-cell lung carcinoma was referred to our department because of a pruritic rash on his head and upper extremities. Prior to the development of the rash, he had received 4 cycles of combination therapy with pemetrexed, carboplatin, and pembrolizumab, followed by 2 cycles of pembrolizumab monotherapy. On physical examination, violaceous scaly erythema grouped on his scalp and upper extremities. Histologically, the scalp lesions demonstrated irregular acanthosis that formed a characteristic saw-tooth appearance with hypergranulosis and typical lichenoid tissue reaction. These findings suggested that the scalp lesions were lichen planus. Two-week administration of topical corticosteroid dramatically improved the rash. Immunotherapy with pembrolizumab, an anti-PD-1 antibody, can induce T-cell activation that results in various immune-related adverse effects such as lichenoid tissue reaction. However, lichen planus is generally found on the extremities and/or oral mucosa, and unlike in this case, the scalp is rarely affected. Although the exact mechanism underlying predominant scalp involvement is unknown, the present case indicates that anti-PD-1 therapy-induced lichen planus can develop not only on the extremities and oral mucosa but also on the scalp. Interestingly, the lesions were not induced by the combination of chemotherapy and pembrolizumab; rather, they occurred soon after initiation of pembrolizumab monotherapy. In the present case, pembrolizumab-induced T-cell activation which triggered lichenoid tissue reaction may have been suppressed by chemotherapy-induced immunosuppression. Dermatologists should have a thorough knowledge of the cutaneous lesions that manifest as irAEs of anti-PD-1 therapy.
一名67岁的非小细胞肺癌男性因头部和上肢出现瘙痒性皮疹而转诊至我科。在皮疹出现之前,他接受了4个周期的培美曲塞、卡铂和帕博利珠单抗联合治疗,随后进行了2个周期的帕博利珠单抗单药治疗。体格检查发现,他的头皮和上肢出现紫红色鳞屑性红斑,呈群集分布。组织学检查显示,头皮病变表现为不规则棘层肥厚,形成特征性的锯齿状外观,伴有颗粒层增厚和典型的苔藓样组织反应。这些发现提示头皮病变为扁平苔藓。局部应用皮质类固醇激素两周后,皮疹明显改善。抗PD -1抗体帕博利珠单抗进行免疫治疗可诱导T细胞活化,导致各种免疫相关不良反应,如苔藓样组织反应。然而,扁平苔藓通常发生在四肢和/或口腔黏膜,与本病例不同的是,头皮很少受累。虽然头皮受累为主的确切机制尚不清楚,但本病例表明,抗PD -1治疗引起的扁平苔藓不仅可发生在四肢和口腔黏膜,也可发生在头皮。有趣的是,这些病变并非由化疗与帕博利珠单抗联合使用引起;相反,它们在帕博利珠单抗单药治疗开始后不久就出现了。在本病例中,化疗诱导的免疫抑制可能抑制了帕博利珠单抗诱导的触发苔藓样组织反应的T细胞活化。皮肤科医生应全面了解作为抗PD -1治疗免疫相关不良反应表现的皮肤病变。