Eosinophilic Fasciitis in a 78-Year-Old Man Following Pembrolizumab Treatment for Bladder Cancer.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Ibiyemi Oke, Aleksander Lenert, Brian L Swick, Petar Lenert
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引用次数: 0

Abstract

BACKGROUND Immune checkpoint inhibitors (ICI) like pembrolizumab are increasingly used in cancer treatment and have become the standard of care for certain types of malignancies. Expanded use of these medications has led to more frequent recognition of immune-related adverse events (irAEs), including those presenting with sclerosing skin conditions such as eosinophilic fasciitis (EF). This case report describes the clinical presentation and management of a 78-year-old man with a history of bladder cancer who developed eosinophilic fasciitis after 6 months of treatment with an ICI. CASE REPORT Following 6 months of treatment with pembrolizumab, the patient developed capillary-leakage syndrome (CLS), which was treated with intravenous immunoglobulin (IVIG) and steroids. Several months after the resolution of his CLS, he developed painful hardening of the skin in his extremities and back, with notable induration of the skin and restricted range of motion across his elbows on physical examination. Laboratory workup revealed elevated inflammatory markers and eosinophilia. Skin biopsy revealed fibrosis of subcutaneous tissue and deep fascia, with multifocal collections of lymphocytes and plasma cells, consistent with eosinophilic fasciitis. Pembrolizumab was discontinued, and he received treatment with prednisone, mycophenolate mofetil, hydroxychloroquine, and benralizumab, with some improvement in his skin lesions. CONCLUSIONS This case report supports the need to have a high index of suspicion and investigate for eosinophilic fasciitis in cancer patients treated with anti-PD-1 medications who present with symmetric, painful hardening of the skin.

78岁男性因膀胱癌接受派姆单抗治疗后的嗜酸性筋膜炎
免疫检查点抑制剂(ICI)如派姆单抗越来越多地用于癌症治疗,并已成为某些类型恶性肿瘤的标准治疗。这些药物的广泛使用导致免疫相关不良事件(irae)的识别更加频繁,包括那些表现为皮肤硬化的情况,如嗜酸性筋膜炎(EF)。本病例报告描述了一位78岁有膀胱癌病史的男性患者在接受ICI治疗6个月后出现嗜酸性筋膜炎的临床表现和处理方法。病例报告:在使用派姆单抗治疗6个月后,患者出现了毛细血管渗漏综合征(CLS),并接受静脉注射免疫球蛋白(IVIG)和类固醇治疗。CLS消退几个月后,患者四肢和背部皮肤出现疼痛性硬化,体格检查显示皮肤明显硬化,肘部活动范围受限。实验室检查显示炎症标志物和嗜酸性粒细胞升高。皮肤活检显示皮下组织和深筋膜纤维化,伴多灶性淋巴细胞和浆细胞聚集,符合嗜酸性筋膜炎。停用派姆单抗,他接受强的松、霉酚酸酯、羟氯喹和苯那利单抗治疗,皮肤病变有所改善。结论:本病例报告支持在接受抗pd -1药物治疗的癌症患者中出现对称性、疼痛性皮肤硬化的嗜酸性筋膜炎的高度怀疑和调查的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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