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病例报告:通过优化阿达木单抗生物类似药与阿维A及孟鲁司特联合使用的剂量来治疗重度毛发红糠疹的重点领域。

Case report: Area of focus of management of severe pityriasis rubra pilaris by dose optimization of adalimumab biosimilar in combination with acitretin and montelukast.

作者信息

Heidemeyer Kristine, Seyed Jafari S Morteza, Farnina Lena, Bossart Simon, Feldmeyer Laurence, Yawalkar Nikhil

机构信息

Department of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

出版信息

Front Med (Lausanne). 2023 Nov 30;10:1295777. doi: 10.3389/fmed.2023.1295777. eCollection 2023.

Abstract

Pityriasis rubra pilaris (PRP) is a rare inflammatory skin disorder characterized by hyperkeratotic follicular papules, orange-red scaling plaques with islands of sparing and palmoplantar keratoderma. While spontaneous resolution occurs in some cases, treatment can be challenging for others. The use of biologics in PRP management has gained attention in recent studies, although their high costs and potential side effects present limitations. We present a case of a 71-year-old patient with treatment-resistant PRP who showed significant improvement through optimized adalimumab treatment. Considering the emerging role of phospholipase A2 in PRP pathogenesis, montelukast was added, further enhancing the therapeutic response. By maintaining montelukast and prolonging the adalimumab interval to 3 and 4 weeks, effective dose optimization was achieved without PRP relapse. This case report highlights the potential for adalimumab dose optimization by shortening the initial treatment interval for increased effectiveness and lengthening the interval during the maintenance phase to conserve medication doses. Montelukast appears to assist in sustaining clinical outcomes during interval prolongation, necessitating further investigation through additional studies.

摘要

红皮病型毛发红糠疹(PRP)是一种罕见的炎症性皮肤病,其特征为角化过度的毛囊丘疹、有正常皮肤岛的橙红色鳞屑斑块以及掌跖角化病。虽然有些病例可自发缓解,但对其他病例而言,治疗可能具有挑战性。尽管生物制剂成本高昂且存在潜在副作用,但在PRP治疗中的应用在最近的研究中受到了关注。我们报告一例71岁治疗抵抗性PRP患者,通过优化阿达木单抗治疗取得显著改善。考虑到磷脂酶A2在PRP发病机制中的新作用,加用了孟鲁司特,进一步增强了治疗反应。通过维持孟鲁司特并将阿达木单抗间隔延长至3周和4周,实现了有效的剂量优化且PRP未复发。本病例报告强调了通过缩短初始治疗间隔以提高疗效、延长维持阶段间隔以节省药物剂量来优化阿达木单抗剂量的潜力。孟鲁司特似乎有助于在延长间隔期间维持临床疗效,需要通过更多研究进行进一步调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5490/10720432/90a84f65eab8/fmed-10-1295777-g001.jpg

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