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维拉帕米成功控制化脓性汗腺炎:一例报告

Successful control of hidradenitis suppurativa with verapamil: a case report.

作者信息

Laroche Marie-Laure, Teste Marianne, Vanoost Julien, Geniaux Hélène

机构信息

Pharmacology, Toxicology and Pharmacovigilance Department, University Hospital of Limoges, CHU de Limoges - 2 avenue Martin Luther King, Limoges Cedex, 87042, France.

Faculty of Medicine, University of Limoges, 2 rue du Dr Marcland Limoges, 87025, Cedex, France.

出版信息

Fundam Clin Pharmacol. 2019 Feb;33(1):122-124. doi: 10.1111/fcp.12403. Epub 2018 Aug 5.

Abstract

An inappropriate immunologic response has been suggested to play a role in the pathogenesis of hidradenitis suppurativa (HS). Adalimumab was the first TNF-α inhibitor approved for moderate to severe HS. We report on a case of HS (Hurley stage 2) in a 39-year-old man, who had received fusidic acid and isotretinoin treatments without evident benefit during the last 8 years. The patient noticed a reduction in the number of lesions and quality of life (DLQI from 27 to 6) in the 2 months following verapamil initiation for cluster headache. When verapamil was stopped, the lesions recurred within 1.5 months. The patient resumed taking verapamil as before and a remission occurred. Verapamil has been shown to inhibit TNF-α and IL-1β in vitro and in vivo. We hypothesize that verapamil inhibits the inflammatory process through the TNF-α/IL-1 pathway involved in the HS physiopathology. Compared to biologic agents as anti-TNF-α (adalimumab) and anti-IL1 (anakinra), verapamil is safer and cheaper. Given its possible role on TNF-α/IL-1, verapamil may represent an alternative therapeutic option in mild and moderate HS.

摘要

一种不适当的免疫反应被认为在化脓性汗腺炎(HS)的发病机制中起作用。阿达木单抗是首个被批准用于治疗中度至重度HS的肿瘤坏死因子-α(TNF-α)抑制剂。我们报告一例39岁男性的HS(Hurley 2期)病例,该患者在过去8年中接受了夫西地酸和异维A酸治疗,但无明显疗效。该患者在开始使用维拉帕米治疗丛集性头痛后的2个月内,注意到皮损数量减少,生活质量(皮肤病生活质量指数从27降至6)改善。当停用维拉帕米时,皮损在1.5个月内复发。患者再次像之前一样服用维拉帕米后病情缓解。维拉帕米已被证明在体外和体内均可抑制TNF-α和白细胞介素-1β(IL-1β)。我们推测维拉帕米通过参与HS病理生理学的TNF-α/IL-1途径抑制炎症过程。与抗TNF-α生物制剂(阿达木单抗)和抗IL-1生物制剂(阿那白滞素)相比,维拉帕米更安全、更便宜。鉴于其对TNF-α/IL-1可能的作用,维拉帕米可能是轻度和中度HS的一种替代治疗选择。

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