Successful Treatment of Cutaneous Foreign Body Granuloma with JAK Inhibitor Abrocitinib and Prednisone: A Case Report.

IF 1.9 4区 医学 Q3 DERMATOLOGY
Clinical, Cosmetic and Investigational Dermatology Pub Date : 2025-05-17 eCollection Date: 2025-01-01 DOI:10.2147/CCID.S522469
Jingqiu Fu, Wen Luo, Ping Wang, Weiwei Wu, Jiejie Lu
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引用次数: 0

Abstract

Background: Foreign body granuloma (FBG) formation is linked to chronic persistent cutaneous inflammation, representing a severe delayed complication characterized histologically by infiltration of multinucleated giant cells and aggregation of lymphocytes. In filler-induced FBG following cosmetic injections, implanted materials represent a key driver of sustained inflammatory responses. Achieving complete resolution remains challenging, with current therapeutic outcomes for FBG being suboptimal. Emerging evidence suggests that Janus kinase (JAK) inhibitors may constitute a promising therapeutic strategy for refractory granulomatous conditions.

Objective: This case report describes the successful management of FBG using JAK inhibitors and synthesizes existing literature to evaluate the efficacy, safety, and potential mechanisms of abrocitinib in treating filler-induced cutaneous FBG.

Methods: We present a case of post-filler FBG that presents with multiple smooth-surfaced, hemispherical lesions (3-5 mm in diameter) distributed across the entire facial region. The patient was treated with oral abrocitinib (100 mg daily) and prednisone (30 mg daily, tapered over 9 weeks). Clinical outcomes were assessed weekly for 13 weeks through serial clinical photography, dermoscopy, reflectance confocal microscopy, and multispectral imaging. Adverse events, including rash exacerbation, vomiting, dizziness, and fever, were systematically monitored. A comprehensive literature review was conducted to elucidate JAK inhibitors' therapeutic rationale in filler-associated FBG.

Results: The patient achieved complete granuloma resolution within 13 weeks following failed corticosteroid monotherapy. No treatment-related adverse effects were observed during the one-month follow-up period, supporting the favorable safety profile of this therapeutic approach.

Conclusion: This report provides preliminary evidence for JAK inhibitors' efficacy in managing refractory filler-induced FBG. Large-scale controlled trials are warranted to validate long-term safety and therapeutic benefits.

JAK抑制剂阿布替尼联合强的松治疗皮肤异物肉芽肿1例。
背景:异物肉芽肿(FBG)的形成与慢性持续性皮肤炎症有关,是一种严重的延迟并发症,其组织学特征是多核巨细胞浸润和淋巴细胞聚集。在美容注射后填充物诱导的FBG中,植入材料是持续炎症反应的关键驱动因素。实现完全解决仍然具有挑战性,目前FBG的治疗结果并不理想。新出现的证据表明,Janus激酶(JAK)抑制剂可能是难治性肉芽肿疾病的一种有希望的治疗策略。目的:本病例报告描述了使用JAK抑制剂成功治疗FBG,并综合现有文献评价阿布替尼治疗填充物诱导的皮肤FBG的有效性、安全性和潜在机制。方法:我们提出一例后填充FBG,呈现多个光滑表面,半球形病变(直径3-5毫米)分布在整个面部区域。患者接受口服阿布替尼(100mg /天)和强的松(30mg /天,9周逐渐减少)治疗。临床结果通过连续临床摄影、皮肤镜检查、反射共聚焦显微镜和多光谱成像每周评估一次,持续13周。系统监测不良事件,包括皮疹加重、呕吐、头晕和发烧。我们进行了一项全面的文献综述,以阐明JAK抑制剂在填充物相关性FBG中的治疗原理。结果:患者在皮质类固醇单药治疗失败后13周内肉芽肿完全消退。在一个月的随访期间没有观察到与治疗相关的不良反应,支持这种治疗方法的良好安全性。结论:本报告为JAK抑制剂治疗难治性填充物诱导的FBG提供了初步证据。需要大规模的对照试验来验证长期的安全性和治疗效果。
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
CiteScore
2.80
自引率
4.30%
发文量
353
审稿时长
16 weeks
期刊介绍: Clinical, Cosmetic and Investigational Dermatology is an international, peer-reviewed, open access journal that focuses on the latest clinical and experimental research in all aspects of skin disease and cosmetic interventions. Normal and pathological processes in skin development and aging, their modification and treatment, as well as basic research into histology of dermal and dermal structures that provide clinical insights and potential treatment options are key topics for the journal. Patient satisfaction, preference, quality of life, compliance, persistence and their role in developing new management options to optimize outcomes for target conditions constitute major areas of interest. The journal is characterized by the rapid reporting of clinical studies, reviews and original research in skin research and skin care. All areas of dermatology will be covered; contributions will be welcomed from all clinicians and basic science researchers globally.
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