Perman Marissa J, Lovell Daniel J, Denson Lee A, Farrell Michael K, Lucky Anne W
Division of Dermatology, College of Medicine, University of Cincinnati and Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Pediatr Dermatol. 2012 Jul-Aug;29(4):454-9. doi: 10.1111/j.1525-1470.2011.01521.x. Epub 2011 Oct 13.
Although anti-tumor necrosis factor alpha (TNF-α) agents are commonly used to treat psoriasis and other inflammatory diseases in adults and children, numerous reports have documented new-onset or flaring psoriasis in adults treated for the other conditions. Individual case reports have documented similar observations in three children. We report a series of anti-TNF-α-induced psoriasis in children with juvenile idiopathic arthritis or inflammatory bowel disease treated at a large children's hospital. All five patients presented with severe scalp involvement. One child was treated with adalimumab for juvenile idiopathic arthritis, and four received infliximab for inflammatory bowel disease. The five patients developed psoriasis 2 to 10 months after initiating anti-TNF-α therapy. They presented with erythematous, scaly, crusted scalp lesions. Three of the five patients were initially treated with griseofulvin for presumed tinea capitis. The anti-TNF-α agent was discontinued at the time of diagnosis in two cases. Topical steroids were the mainstay of psoriasis therapy, with improvement in four of five patients. Anti-TNF-α agents have been associated with the onset or worsening of psoriasis in adults, but this has rarely been reported in children. We describe five pediatric cases of anti-TNF-α-induced psoriasis presenting with severe scalp involvement and review their subsequent management. We hope that clinicians caring for patients receiving anti-TNF-α agents will consider psoriasis from the onset of cutaneous symptoms and institute appropriate therapy or referral.
尽管抗肿瘤坏死因子α(TNF-α)药物常用于治疗成人和儿童的银屑病及其他炎症性疾病,但众多报告记录了在因其他病症接受治疗的成人中出现新发或银屑病病情加重的情况。个别病例报告记录了在三名儿童中也有类似的观察结果。我们报告了在一家大型儿童医院接受治疗的患有幼年特发性关节炎或炎症性肠病的儿童中一系列抗TNF-α诱导的银屑病病例。所有五名患者均有严重的头皮受累情况。一名儿童因幼年特发性关节炎接受阿达木单抗治疗,四名儿童因炎症性肠病接受英夫利昔单抗治疗。这五名患者在开始抗TNF-α治疗后2至10个月出现银屑病。他们表现为头皮有红斑、鳞屑、结痂性病变。五名患者中有三名最初因疑似头癣接受灰黄霉素治疗。两例在诊断时停用了抗TNF-α药物。局部用类固醇是银屑病治疗的主要方法,五名患者中有四名病情改善。抗TNF-α药物与成人银屑病的发作或病情恶化有关,但在儿童中很少有报道。我们描述了五例以严重头皮受累为表现的抗TNF-α诱导的儿童银屑病病例,并回顾了其后续治疗情况。我们希望为接受抗TNF-α药物治疗的患者提供护理的临床医生从皮肤症状出现时就考虑到银屑病,并进行适当的治疗或转诊。