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一名伴有哮喘的泛发性脓疱型银屑病患者使用白细胞介素-17A抑制剂后出现的矛盾性湿疹

Paradoxical Eczema Associated With Interleukin-17A Inhibitor Use in a Patient With Generalized Pustular Psoriasis Accompanied by Asthma.

作者信息

Yatsuzuka Kazuki, Muto Jun, Shiraishi Ken, Fujisawa Yasuhiro, Murakami Masamoto

机构信息

Department of Dermatology, Ehime University Graduate School of Medicine, Toon, JPN.

出版信息

Cureus. 2024 Jul 16;16(7):e64680. doi: 10.7759/cureus.64680. eCollection 2024 Jul.

Abstract

Although rare, paradoxical eczema (PE) is an adverse event associated with the use of biological agents to treat psoriasis, particularly in patients with atopic predispositions. We report the first case of severe PE induced by secukinumab in a patient with generalized pustular psoriasis (GPP) and asthma. A woman in her 50s with a history of interstitial nephritis attributable to Sjogren's syndrome experienced a flare-up of GPP after discontinuing mycophenolate mofetil and was hospitalized. Treatment with secukinumab accompanied by an increased prednisolone level afforded rapid improvement, but she subsequently developed widespread, itchy, serous papules and erythema. A biopsy confirmed that the erythema was an eczematous reaction, thus PE. Her condition improved after switching from secukinumab to deucravacitinib with a temporary increase in the prednisolone level; no recurrence of GPP or PE was observed for 11 months. Elevated serum levels of interleukin (IL)-17A, IL-22, and the Th2 chemokine TARC recorded at the onset time of PE suggested that these mediators contributed to the observed pathology. Our case highlights the need for careful consideration when prescribing IL-17 inhibitors to patients with GPP, particularly those with atopic predispositions, given the potential activation of the Th2 axis and thus severe eczematous reactions. Further research is required to understand the essential nature of PE in patients with GPP and the roles of IL-17A and IL-22 in this context.

摘要

虽然罕见,但矛盾性湿疹(PE)是一种与使用生物制剂治疗银屑病相关的不良事件,尤其是在有特应性倾向的患者中。我们报告了第一例由司库奇尤单抗诱发的严重PE病例,该患者患有泛发性脓疱型银屑病(GPP)和哮喘。一名50多岁有干燥综合征所致间质性肾炎病史的女性,在停用霉酚酸酯后GPP病情加重并住院。使用司库奇尤单抗治疗并提高泼尼松龙水平后病情迅速改善,但随后她出现了广泛的、瘙痒的、浆液性丘疹和红斑。活检证实红斑为湿疹样反应,即PE。从司库奇尤单抗换用德卡伐替尼并暂时提高泼尼松龙水平后,她的病情有所改善;11个月内未观察到GPP或PE复发。PE发作时记录的血清白细胞介素(IL)-17A、IL-22和Th2趋化因子TARC水平升高,提示这些介质促成了观察到的病理变化。我们的病例强调,在给GPP患者,尤其是有特应性倾向的患者开IL-17抑制剂时,鉴于Th2轴可能被激活从而引发严重的湿疹样反应,需要谨慎考虑。需要进一步研究以了解GPP患者中PE的本质以及IL-17A和IL-22在此背景下的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/523c/11326853/619bd73b5b7d/cureus-0016-00000064680-i01.jpg

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