Department of Dermatology, S. Elia Hospital, Via Luigi Russo 6, Caltanissetta (CL), Italy.
Dermatol Ther. 2010 Sep-Oct;23(5):541-3. doi: 10.1111/j.1529-8019.2010.01357.x.
Pyoderma gangrenosum (PG) is a rare, noninfectious, neutrophilic dermatosis of unknown origin that is associated with systemic diseases in 50% of cases. The authors present a case of a 54-year-old man patient with refractory to conventional treatment PG associated with ulcerative colitis and psoriasis, which showed a successful response to treatment with infliximab, a chimeric monoclonal antibody that inhibits tumor necrosis factor alpha (TNF-α). This case report shows the frequent difficulty in the therapeutic approach of PG, especially if associated with underlying disease, and necessity to apply new agents, such as a novel application of the TNF-α inhibitors, in relationship to the recent pathogenic knowledge.
坏疽性脓皮病(PG)是一种罕见的、非传染性的中性粒细胞性皮肤病,病因不明,50%的病例与系统性疾病有关。作者报告了一例 54 岁男性患者,患有难治性 PG,与溃疡性结肠炎和银屑病有关,用英夫利昔单抗(一种抑制肿瘤坏死因子-α(TNF-α)的嵌合单克隆抗体)治疗后取得了成功的反应。本病例报告显示了 PG 的治疗方法经常存在困难,特别是如果与潜在疾病有关,并且需要应用新的药物,如 TNF-α抑制剂的新应用,与最近的发病机制知识有关。