Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Pace, 9, 20122, Milan, Italy.
Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.
Am J Clin Dermatol. 2022 Sep;23(5):615-634. doi: 10.1007/s40257-022-00699-8. Epub 2022 May 24.
Pyoderma gangrenosum is a rare inflammatory skin disease classified within the group of neutrophilic dermatoses and clinically characterized by painful, rapidly evolving cutaneous ulcers with undermined, irregular, erythematous-violaceous edges. Pyoderma gangrenosum pathogenesis is complex and involves a profound dysregulation of components of both innate and adaptive immunity in genetically predisposed individuals, with the follicular unit increasingly recognized as the putative initial target. T helper 17/T helper 1-skewed inflammation and exaggerated inflammasome activation lead to a dysregulated neutrophil-dominant milieu with high levels of tumor necrosis factor-α, interleukin (IL)-1β, IL-1α, IL-8, IL-12, IL-15, IL-17, IL-23, and IL-36. Low-evidence studies and a lack of validated diagnostic and response criteria have hindered the discovery and validation of new effective treatments for pyoderma gangrenosum. We review established and emerging treatments for pyoderma gangrenosum. A therapeutic algorithm based on available evidence is also provided. For emerging treatments, we review target molecules and their role in the pathogenesis of pyoderma gangrenosum.
坏疽性脓皮病是一种罕见的炎症性皮肤病,属于中性粒细胞皮肤病组,临床上以疼痛、迅速发展的皮肤溃疡为特征,边缘有侵蚀、不规则、红斑-紫色。坏疽性脓皮病的发病机制很复杂,涉及到遗传易感性个体固有和适应性免疫成分的深刻失调,毛囊单位越来越被认为是最初的假定靶标。辅助性 T 细胞 17/辅助性 T 细胞 1 倾斜性炎症和过度炎症小体激活导致失调的中性粒细胞主导环境,高水平的肿瘤坏死因子-α、白细胞介素(IL)-1β、IL-1α、IL-8、IL-12、IL-15、IL-17、IL-23 和 IL-36。低证据研究和缺乏经过验证的诊断和反应标准阻碍了新的有效的坏疽性脓皮病治疗方法的发现和验证。我们回顾了坏疽性脓皮病的既定和新兴治疗方法。还提供了基于现有证据的治疗算法。对于新兴的治疗方法,我们回顾了靶分子及其在坏疽性脓皮病发病机制中的作用。