在更新他替尼治疗特应性皮炎期间白癜风恶化和改用阿布替尼后的改善:一个病例报告。

IF 3.9
Zhaoyang Wang, Meng Wang, Yonghu Sun
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引用次数: 0

摘要

目的:Janus激酶(JAK)抑制剂已成为特应性皮炎(AD)的靶向治疗方法,越来越多的证据表明它们对白癜风有潜在的益处。虽然这两种疾病被认为在免疫学上是不同的,但最近的见解指出,重叠的细胞因子通路可能由jak1选择性抑制剂调节。材料和方法:我们报告了一例37岁男性,患有中重度AD和稳定型白癜风,在upadacitinib治疗后白癜风恶化。虽然阿尔茨海默病症状消退,白癜风病变进展,尽管光疗。结果:从upadacitinib切换到abrocitinib后,患者在三个月内经历了白癜风病变的显着重新着色,同时AD症状继续得到控制。结论:该病例突出了upadacitinib和abrocitinib的不同作用,可能是由于它们不同的JAK2抑制谱。这些发现强调了在重叠免疫介导的皮肤病患者中使用JAK抑制剂时考虑激酶选择性的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vitiligo exacerbation during upadacitinib treatment for atopic dermatitis and improvement following a switch to abrocitinib: a case report.

Aim: Janus kinase (JAK) inhibitors have emerged as targeted therapies for atopic dermatitis (AD), and increasing evidence suggests their potential benefit in vitiligo. While both diseases are considered immunologically distinct, recent insights point to overlapping cytokine pathways that may be modulated by JAK1-selective inhibitors.

Materials and methods: We present a case of a 37-year-old male with moderate-to-severe AD and stable vitiligo who developed worsening of vitiligo following treatment with upadacitinib. Although AD symptoms resolved, vitiligo lesions progressed despite phototherapy.

Results: After switching from upadacitinib to abrocitinib, the patient experienced marked repigmentation of vitiligo lesions within three months, along with continued control of AD symptoms.

Conclusions: This case highlights the differential effects of upadacitinib and abrocitinib, possibly due to their distinct JAK2 inhibition profiles. The findings underscore the importance of considering kinase selectivity when using JAK inhibitors in patients with overlapping immune-mediated skin disorders.

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