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用比美吉珠单抗成功治疗的哈洛佩奥连续性肢端皮炎:一例报告

Acrodermatitis continua of Hallopeau successfully treated with bimekizumab: A case report.

作者信息

Cirone Katrina D, Lovegrove Fiona E

机构信息

Schulich School of Medicine & Dentistry, Western University, London, ON, Canada.

Lovegrove Dermatology, London, ON, Canada.

出版信息

SAGE Open Med Case Rep. 2023 Mar 21;11:2050313X231160937. doi: 10.1177/2050313X231160937. eCollection 2023.

Abstract

Acrodermatitis continua of Hallopeau is a rare variant of localized pustular psoriasis characterized by the recurrent eruption of sterile pustules involving the distal portions of the fingers and toes that can lead to the destruction of the nail apparatus. Acrodermatitis continua of Hallopeau is a chronic, relapsing condition that is resistant to most topical and systemic psoriasis therapies, making it notoriously difficult to manage. Interleukin-36 and interleukin-17 are thought to play a pivotal role in the pathophysiology of pustular psoriasis, and evidence suggests that interleukin-17 inhibition can be an effective therapy for pustular psoriasis variants, including acrodermatitis continua of Hallopeau. Bimekizumab, a monoclonal antibody that inhibits the interleukin-17 pathway, may be a safe and effective treatment option for patients with acrodermatitis continua of Hallopeau. We present the first documented case of a patient with acrodermatitis continua of Hallopeau of the bilateral thumbnails who experienced an excellent response to bimekizumab treatment.

摘要

哈洛佩au连续性肢端皮炎是局限性脓疱型银屑病的一种罕见变体,其特征是无菌性脓疱反复出现在手指和脚趾的远端部分,可导致甲器破坏。哈洛佩au连续性肢端皮炎是一种慢性复发性疾病,对大多数局部和全身性银屑病治疗均有抵抗性,因此极难治疗。白细胞介素-36和白细胞介素-17被认为在脓疱型银屑病的病理生理学中起关键作用,有证据表明抑制白细胞介素-17可能是脓疱型银屑病变体(包括哈洛佩au连续性肢端皮炎)的有效治疗方法。比美吉珠单抗是一种抑制白细胞介素-17通路的单克隆抗体,可能是哈洛佩au连续性肢端皮炎患者的一种安全有效的治疗选择。我们报告了首例双侧拇指甲患有哈洛佩au连续性肢端皮炎的患者对比美吉珠单抗治疗反应良好的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fddc/10034280/e35404db63a0/10.1177_2050313X231160937-fig1.jpg

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