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依法利珠单抗治疗下红皮病型毛发红糠疹病情加重。

Exacerbation of pityriasis rubra pilaris under efalizumab therapy.

作者信息

Klein A, Szeimies R-M, Landthaler M, Karrer S

机构信息

Department of Dermatology, University of Regensburg, Regensburg, Germany.

出版信息

Dermatology. 2007;215(1):72-5. doi: 10.1159/000102039.

Abstract

A 60-year-old woman, diagnosed as having psoriasis vulgaris in 2004 and unresponsive to standard therapies, received weekly subcutaneous injections with efalizumab. Within 9 weeks of treatment a massive aggravation of skin lesions occurred with widespread orange-tinged erythroderma, islands of normal skin on the back and the inner side of the forearms and palmoplantar hyperkeratosis. A biopsy confirmed the clinical diagnosis of pityriasis rubra pilaris. After discontinuation of efalizumab and treatment with oral corticosteroids, acitretin (30 mg/day) and PUVA therapy, the skin lesions continuously improved. Efalizumab, a fully humanized monoclonal antibody against CD11a, inhibits various T cell processes important in the pathogenesis of psoriasis. Efalizumab has been approved for the treatment of moderate to severe psoriasis, but there are no reports in the literature on the use of efalizumab for pityriasis rubra pilaris.

摘要

一名60岁女性,2004年被诊断为寻常型银屑病,对标准治疗无反应,接受了依法利珠单抗每周一次的皮下注射。治疗9周内,皮肤病变出现大规模加重,伴有广泛的橙红色红皮病、背部及前臂内侧的正常皮肤岛以及掌跖角化过度。活检证实了毛发红糠疹的临床诊断。停用依法利珠单抗并采用口服皮质类固醇、阿维A(30毫克/天)和光化学疗法治疗后,皮肤病变持续改善。依法利珠单抗是一种针对CD11a的全人源化单克隆抗体,可抑制银屑病发病机制中重要的各种T细胞过程。依法利珠单抗已被批准用于治疗中度至重度银屑病,但文献中尚无关于依法利珠单抗用于毛发红糠疹治疗的报道。

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