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在帕博利珠单抗治疗膀胱癌期间发生的急性痘疮样苔藓状糠疹。

Pityriasis Lichenoides et Varioliformis Acuta Developing during Pembrolizumab Treatment for Bladder Cancer.

作者信息

Mizutani Yuki, Noda Ena, Kondo Makoto, Hayashi Akinobu, Yamanaka Keiichi

机构信息

Department of Dermatology, Graduate School of Medicine, Mie University, Tsu, Japan.

Department of Oncologic Pathology, Graduate School of Medicine, Mie University, Tsu, Japan.

出版信息

Case Rep Dermatol. 2024 May 17;16(1):116-122. doi: 10.1159/000538767. eCollection 2024 Jan-Dec.

Abstract

INTRODUCTION

Anti-PD-1 immunotherapies enhance T-cell responses against tumor cells by blocking the interaction between PD-1 and its ligand, PD-L1. While these therapies offer significant benefits in treating various malignancies, they can also lead to several immune-related adverse events (irAEs), most notably manifesting in the skin. Lichenoid reactions, eczema, and vitiligo are the three most prevalent forms of cutaneous irAE.

CASE PRESENTATION

Here, we report a rare case of a pityriasis lichenoides et varioliformis acuta (PLEVA) that developed during pembrolizumab treatment for invasive bladder cancer. A 53-year-old man, receiving pembrolizumab for invasive bladder cancer, developed erythematous papules on his legs after his 11th infusion. The skin lesions gradually spread to his entire trunk and extremities. A punch biopsy revealed several apoptotic keratinocytes and spongiosis, along with perivascular and lichenoid lymphocytic infiltration with vacuolar alteration. Immunohistochemistry showed infiltration of CD4+ and CD8+ T cells in both the epidermis and dermis. Granzyme B-positive inflammatory cells were also slightly present. From these results, he was diagnosed with PLEVA, which might be classified as a lichenoid eruption, especially based on the histological findings.

CONCLUSION

We hypothesize that the anti-PD-1 antibody might lead to epidermal necrosis by amplifying the expression of cytolytic molecules such as granzyme B in CD8+ T cells.

摘要

引言

抗程序性死亡蛋白1(PD-1)免疫疗法通过阻断PD-1与其配体程序性死亡配体1(PD-L1)之间的相互作用来增强T细胞对肿瘤细胞的反应。虽然这些疗法在治疗各种恶性肿瘤方面有显著益处,但它们也可能导致一些免疫相关不良事件(irAE),最明显的表现是在皮肤上。苔藓样反应、湿疹和白癜风是皮肤irAE最常见的三种形式。

病例报告

在此,我们报告1例在使用帕博利珠单抗治疗浸润性膀胱癌期间发生急性痘疮样苔藓状糠疹(PLEVA)的罕见病例。一名53岁男性因浸润性膀胱癌接受帕博利珠单抗治疗,在第11次输注后腿部出现红斑丘疹。皮肤病变逐渐蔓延至其整个躯干和四肢。皮肤活检显示有多个凋亡角质形成细胞和海绵形成,伴有血管周围和苔藓样淋巴细胞浸润及空泡改变。免疫组织化学显示表皮和真皮均有CD4+和CD8+T细胞浸润。也有少量颗粒酶B阳性炎性细胞。根据这些结果,他被诊断为PLEVA,尤其是基于组织学表现,其可能被归类为苔藓样皮疹。

结论

我们推测抗PD-1抗体可能通过放大CD8+T细胞中颗粒酶B等溶细胞分子的表达而导致表皮坏死。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2405/11250282/06d78b4887b3/cde-2024-0016-0001-538767_F01.jpg

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