Fernandes Iolanda C, Torres Tiago, Sanches Madalena, Velho Glória, Lago Paula, Selores Manuela
Serviço de Dermatologia, Hospital de Santo António, Porto, Portugal.
Acta Med Port. 2011 Dec;24 Suppl 3:709-12. Epub 2011 Dec 31.
Recently, the tumor necrosis factor-α inhibitors (anti-TNF-α) have been extensively used in clinical practice, in the treatment of several immune-mediated disorders, such as inflammatory bowel diseases, rheumatoid arthritis and more recently in psoriasis.
A 35-year-old woman, suffering from Crohn's disease, diagnosed in 1994, successfully treated with infliximab at the dosage of 5 mg/Kg every 8 weeks, since 10 months ago, was referred to our Dermatology Department due to the development of erythematic-scaling confluent plaques on the scalp, back and umbilical fold. The skin biopsy confirmed the clinical diagnosis of psoriasis. Given the severity of the skin lesions and its relation with the anti-TNF-α, we decided to discontinue infliximab.
Psoriasis results from the combination of polygenic predisposition and several triggering factors. Paradoxically, it has been described an increase of psoriasis induced by biologic agents. The pathogenic mechanism of such paradoxical effect has not yet been clearly elucidated.
近年来,肿瘤坏死因子-α抑制剂(抗TNF-α)已广泛应用于临床实践,用于治疗多种免疫介导的疾病,如炎症性肠病、类风湿性关节炎,最近还用于治疗银屑病。
一名35岁女性,1994年被诊断为克罗恩病,自10个月前起每8周接受5mg/kg剂量的英夫利昔单抗治疗,效果良好。因头皮、背部和脐周出现红斑鳞屑性融合斑块,转诊至我院皮肤科。皮肤活检确诊为银屑病。鉴于皮肤病变的严重程度及其与抗TNF-α的关系,我们决定停用英夫利昔单抗。
银屑病是由多基因易感性和多种触发因素共同作用导致的。矛盾的是,已有生物制剂诱发银屑病增多的报道。这种矛盾效应的致病机制尚未完全阐明。