A Case Report of JAK Inhibitors Therapy for Adult-Onset Still’s Disease with Persistent Pruritic Lesions

Li Tang, Hongjian Shi, Weijun Liu, Pingxiu He, Chun Huang, Xiaobing Wang
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Abstract

Background and Objective

Adult-onset Still’s disease (AOSD) is a recognized autoinflammatory disorder of unknown etiology. The standard initial management for AOSD includes conventional corticosteroids and disease-modifying antirheumatic drugs. In cases that are resistant to these treatments, additional therapeutic options such as immunosuppressants, biologics, and other alternative treatments may be considered. Yet, a significant proportion of patients remain unresponsive to these therapeutic interventions. Herein, a case is reported involving a patient with AOSD who had persistent pruritic lesions that did not respond to conventional therapy, but were alleviated with Janus kinase inhibitors (JAKi), namely baricitinib and upadacitinib. The objective is to expand the number of refractory AOSD cases treated with JAKi in clinical practice. Another aim is to offer potentially effective therapeutic options for AOSD patients who experience persistent pruritus.

Methods

A case was reported involving AOSD characterized by persistent pruritic lesions that failed to respond to conventional treatment, but showed favorable outcomes with JAKi therapy. An analysis of the PubMed literature was performed to assess the medication’s efficacy and explore possible mechanisms.

Results

The present case study is one of the few documented instances exploring the use of JAKi for treating AOSD, aligning with previously published research. After initiating JAKi therapy, the patient exhibited significant improvement in symptoms, most notably a reduction in persistent pruritus. Additionally, there was a substantial decrease in the patient’s glucocorticoid dosage. Aside from minor renal function anomalies, no adverse reactions were observed.

Conclusions

The present case illustrates that JAKi can provide rapid and sustained clinical improvement in patients with AOSD, especially those who have not responded to conventional treatment, and they have the ability to alleviate persistent itching. Further investigation is needed to ascertain the precise mechanism.

Abstract Image

JAK 抑制剂治疗伴有持续性瘙痒皮损的成年型 Still's 病病例报告
背景和目的早发性斯蒂尔病(AOSD)是一种公认的病因不明的自身炎症性疾病。AOSD 的标准初始治疗方法包括常规皮质类固醇激素和改善病情的抗风湿药物。对这些治疗方法产生耐药性的病例,可考虑使用免疫抑制剂、生物制剂和其他替代疗法。然而,仍有相当一部分患者对这些治疗干预无效。本文报告了一例AOSD患者的病例,该患者的瘙痒性皮损持续存在,对常规治疗无效,但使用Janus激酶抑制剂(JAKi),即巴利昔尼(baricitinib)和乌帕替尼(upadacitinib)后病情有所缓解。我们的目标是在临床实践中增加使用JAKi治疗难治性AOSD病例的数量。方法报告了一例以持续性瘙痒病变为特征的AOSD病例,该病例对常规治疗无效,但在接受JAKi治疗后显示出良好的疗效。对PubMed上的文献进行了分析,以评估该药物的疗效并探讨可能的机制。结果本病例研究是为数不多的探讨使用JAKi治疗AOSD的文献之一,与之前发表的研究结果一致。在开始接受JAKi治疗后,患者的症状有了明显改善,最显著的是持续性瘙痒减轻。此外,患者的糖皮质激素用量也大幅减少。除了轻微的肾功能异常外,未观察到任何不良反应。结论本病例表明,JAKi 能使 AOSD 患者的临床症状得到快速、持续的改善,尤其是那些对常规治疗无效的患者,而且它们还能缓解持续性瘙痒。需要进一步研究以确定其确切机制。
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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