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特比萘芬诱发的亚急性皮肤型红斑狼疮在两名系统性红斑狼疮患者中,经局部使用皮质类固醇成功治疗。

Terbinafine-induced subacute cutaneous lupus erythematosus in two patients with systemic lupus erythematosus successfully treated with topical corticosteroids.

作者信息

Kalińska-Bienias Agnieszka, Kowalewski Cezary, Woźniak Katarzyna

机构信息

Department of Dermatology and Immunodermatology, Medical University of Warsaw, Poland. Head: Prof. Cezary Kowalewski MD, PhD.

出版信息

Postepy Dermatol Alergol. 2013 Aug;30(4):261-4. doi: 10.5114/pdia.2013.37038. Epub 2013 Aug 27.

Abstract

So far in the literature there have been reported only 5 patients with a recognized and well-documented history of systemic lupus erythematosus (SLE) who developed SCLE after terbinafine introduction. Here we report two women suffering from SLE who developed SCLE after initiation of oral terbinafine for onychomycosis. Skin lesions in both of them were extensive, located on the trunk, and upper and lower extremities. No exacerbation of SLE symptoms was observed at that time. Despite severe skin lesions, patients revealed good response to topical corticosteroids within a few weeks. The systemic review of the literature and our experience on terbinafine-induced SCLE developing in patients with SLE allowed to create a description for this special subset: a) terbinafine-induced SCLE usually develop in 1-8 weeks after terbinafine introduction, b) skin lesions are usually severe, disseminated including lower extremities, c) patients present Ro/SS-A La/SS-B antibodies, but anti-histone antibodies are rarely observed, d) exacerbation of SLE symptoms is rather not observed, e) eruptions clear within 2-8 weeks, f) withdrawal of terbinafine and topical corticosteroids should be considered as a first-line therapy in these cases, g) terbinafine should be carefully used in patients suffering from SLE.

摘要

迄今为止,文献中仅报道了5例有明确且充分记录的系统性红斑狼疮(SLE)病史的患者,在使用特比萘芬后发生了亚急性皮肤型红斑狼疮(SCLE)。在此,我们报告2例患有SLE的女性,在开始口服特比萘芬治疗甲癣后发生了SCLE。她们两人的皮肤损害都很广泛,位于躯干以及上下肢。当时未观察到SLE症状加重。尽管皮肤损害严重,但患者在几周内对局部使用糖皮质激素显示出良好反应。对文献的系统回顾以及我们关于SLE患者发生特比萘芬诱发的SCLE的经验,使得能够对这一特殊亚组进行如下描述:a)特比萘芬诱发的SCLE通常在使用特比萘芬后1 - 8周内发生,b)皮肤损害通常严重,呈播散性,包括下肢,c)患者存在Ro/SS - A、La/SS - B抗体,但很少观察到抗组蛋白抗体,d)相当未观察到SLE症状加重,e)皮疹在2 - 8周内消退,f)在这些病例中,应将停用特比萘芬和局部使用糖皮质激素视为一线治疗方法,g)对于患有SLE的患者,应谨慎使用特比萘芬。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fff/3834709/e763c400efac/PDIA-30-21272-g001.jpg

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