Suppr超能文献

以依奇珠单抗治疗 Hallopeau 连续性肢端皮炎。

Treatment of acrodermatitis continua of hallopeau with ixekizumab.

机构信息

Skin Care Physicians of Georgia, Macon, GA, USA.

Mercer University School of Medicine, Macon, GA, USA.

出版信息

J Dermatolog Treat. 2021 Feb;32(1):117-119. doi: 10.1080/09546634.2019.1628170. Epub 2019 Jul 5.

Abstract

Acrodermatitis continua of hallopeau (ACH) is a rare chronic inflammatory variant of pustular psoriasis often restricted to the distal portions the digits in the hands and feet. ACH is of a chronic relapsing nature and is invariably recalcitrant to many available topical and systemic anti-psoriatic therapies. On account of its low prevalence and high resistance to treatments, no clinical guideline of ACH exists. We present a patient with ACH resistant to multiple therapies, including the biologic adalimumab, who was successfully treated with an IL-17 inhibitor (ixekizumab). We believe our unique treatment with an excellent outcome may assist other dermatologists if faced with this condition.

摘要

掌跖脓疱性银屑病(Acrodermatitis continua of hallopeau,ACH)是一种罕见的慢性炎症性脓疱型银屑病变异型,通常局限于手部和脚部的远端指(趾)。ACH 具有慢性复发性,并且对许多可用的局部和全身抗银屑病治疗均具有抗性。由于其患病率低且对治疗的抵抗力高,ACH 目前尚无临床指南。我们报告了一例 ACH 患者,该患者对多种治疗方法(包括生物制剂阿达木单抗)均有耐药性,后成功接受了 IL-17 抑制剂(依奇珠单抗)治疗。我们相信,如果其他皮肤科医生遇到这种情况,我们独特的治疗方法和极佳的疗效可能会有所帮助。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验