PD-1 Inhibitor Induced Hypertrophic Lichen Planus: A Case Report.

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Drugs in Research & Development Pub Date : 2024-06-01 Epub Date: 2024-06-15 DOI:10.1007/s40268-024-00461-x
Olivia Lim, Eamonn Maher, Daniel D Miller
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引用次数: 0

Abstract

Background and objective: PD-1 inhibitors have revolutionized cancer therapies and are being used to treat an expanding array of cancers. To best serve patients, clinicians should be familiar with the spectrum of skin manifestations associated with PD-1 inhibitor therapy. Here, we report a unique case of hypertrophic lichen planus (HLP) in a 64-year-old man treated with pembrolizumab; the presentation initially suggested a squamous cell carcinoma (SCC) morphology, then evolved into a morphology more typical of hypertrophic lichen planus. This case underscores the need for caution in diagnosing eruptive SCCs associated with PD-1 inhibitor therapy. In such instances, maintaining a high suspicion for lichenoid reactions as sequelae of PD-1 inhibitor treatment and starting an empiric trial of therapy for lichenoid dermatitis may be warranted to ensure timely management of lesions.

Methods: We describe a case of hypertrophic lichen planus mimicking squamous cell carcinoma in the setting of PD-1 inhibitory therapy with pembrolizumab. A PubMed literature review was conducted to identify other cases and determine the incidence of lichenoid reactions imitating squamous cell carcinoma in the setting of PD-1 inhibitor use.

Results: Our case is one of the few available pieces of literature describing eruptive hypertrophic lichen planus imitating SCC in the setting of PD-1 inhibitor use. Initial skin nodule biopsy appeared histologically compatible with squamous cell carcinoma. Repeat biopsy of the skin lesions revealed histological features consistent with hypertrophic lichen planus. Over time, lower extremity lesions evolved into a more typical appearance of hypertrophic lichen planus. Treatment with topical 0.05% clobetasol ointment and oral acitretin 25 mg led to complete resolution of lesions within 2-3 months.

Conclusions: This case underscores the significance of maintaining vigilance for lichenoid reactions as potential sequelae of PD-1 inhibitor therapy. It highlights the variability in initial presentation and the potential for lesions to transform over time. Timely recognition and appropriate management, including high-potency topical corticosteroids and oral acitretin, are crucial for achieving favorable outcomes in patients experiencing such reactions. More studies are necessary to fully analyze the rate of HLP occurrence as a consequence of PD-1 inhibitor use.

Abstract Image

PD-1 抑制剂诱发的肥厚性扁平苔藓:病例报告。
背景和目的:PD-1 抑制剂已彻底改变了癌症疗法,目前正被用于治疗越来越多的癌症。为更好地服务患者,临床医生应熟悉与 PD-1 抑制剂治疗相关的各种皮肤表现。在此,我们报告了一例独特的肥厚性扁平苔藓(HLP)病例,患者是一名接受过 Pembrolizumab 治疗的 64 岁男性;该病例最初表现为鳞状细胞癌(SCC)形态,随后演变为更典型的肥厚性扁平苔藓形态。该病例强调,在诊断与 PD-1 抑制剂治疗相关的爆发性 SCC 时需要谨慎。在这种情况下,应高度怀疑类苔藓样反应是 PD-1 抑制剂治疗的后遗症,并开始对类苔藓样皮炎进行经验性治疗试验,以确保及时处理病变:我们描述了一例在使用pembrolizumab进行PD-1抑制剂治疗时出现的模仿鳞状细胞癌的肥厚性扁平苔藓。我们对PubMed上的文献进行了查阅,以确定其他病例,并确定在使用PD-1抑制剂的情况下模仿鳞状细胞癌的苔藓样反应的发生率:我们的病例是为数不多的描述在使用PD-1抑制剂的情况下模仿鳞状细胞癌的爆发性肥厚性扁平苔藓的文献之一。最初的皮肤结节活检在组织学上与鳞状细胞癌相符。再次对皮损进行活检发现,组织学特征与肥厚性扁平苔藓一致。随着时间的推移,下肢皮损演变成更典型的肥厚性扁平苔藓。外用 0.05% 氯倍他索软膏和口服阿昔曲汀 25 毫克治疗后,皮损在 2-3 个月内完全消退:本病例强调了对 PD-1 抑制剂治疗的潜在后遗症苔癣样反应保持警惕的重要性。结论:本病例强调了对作为 PD-1 抑制剂治疗潜在后遗症的苔癣样反应保持警惕的重要性,突出了初始表现的可变性和皮损随时间变化的可能性。及时发现并采取适当的治疗措施,包括高效外用皮质类固醇激素和口服阿昔曲汀,对于此类反应患者获得良好的治疗效果至关重要。要全面分析使用 PD-1 抑制剂导致的 HLP 发生率,还需要进行更多的研究。
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来源期刊
Drugs in Research & Development
Drugs in Research & Development Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.10
自引率
0.00%
发文量
31
审稿时长
8 weeks
期刊介绍: Drugs in R&D is an international, peer reviewed, open access, online only journal, and provides timely information from all phases of drug research and development that will inform clinical practice. Healthcare decision makers are thus provided with knowledge about the developing place of a drug in therapy. The Journal includes: Clinical research on new and established drugs; Preclinical research of direct relevance to clinical drug development; Short communications and case study reports that meet the above criteria will also be considered; Reviews may also be considered.
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