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一例儿童患者使用度普利尤单抗后引发脓疱型银屑病。

A pediatric case of dupilumab-induced pustular psoriasis.

机构信息

Department of Dermatology, Children's Hospital of Zhejiang University School of Medicine, Hangzhou.

出版信息

J Dermatolog Treat. 2024 Dec;35(1):2333016. doi: 10.1080/09546634.2024.2333016. Epub 2024 Jun 5.

Abstract

Dupilumab is a novel treatment agent for moderate to severe atopic dermatitis (AD) with few adverse effects. Drug-induced psoriasiform lesions are rare. We report a 4-year-old boy with AD who developed pustular psoriasis during treatment with dupilumab. Pustular psoriasis appeared within 1 week of treatment and worsened in the second week. After stopping dupilumab administration, topical corticosteroids (desonide and mometasone furoate creams) and oral desloratadine without relief. Pustular psoriasis was confirmed by pathological examination, and thiamphenicol was administered. After 2 weeks of treatment, the lesions nearly resolved without recurrence in 1-year follow-up. Dupilumab-induced pustular psoriasis is rare in children.

摘要

度普利尤单抗是一种新型治疗中度至重度特应性皮炎(AD)的药物,副作用较少。药物诱导的银屑病样病变较为罕见。我们报告了一例 4 岁男孩在使用度普利尤单抗治疗期间发生脓疱性银屑病。脓疱性银屑病在治疗后 1 周内出现,并在第 2 周加重。停止度普利尤单抗治疗后,外用皮质类固醇(地奈德和糠酸莫米松乳膏)和口服地氯雷他定无效。脓疱性银屑病通过病理检查得到确认,并给予了氯霉素。治疗 2 周后,皮损几乎消退,1 年随访无复发。度普利尤单抗诱导的脓疱性银屑病在儿童中较为罕见。

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