Riera Julia, Musuruana Jorge, Costa Cecilia, Cavallasca Javier
Hospital JB Iturraspe, Rheumatology and Autoimmune Diseases, Santa Fe, Argentina.
Arch Rheumatol. 2020 Jan 8;35(3):449-453. doi: 10.46497/ArchRheumatol.2020.7498. eCollection 2020 Sep.
Pyoderma gangrenosum (PG) is a neutrophilic dermatosis that most often presents with painful ulcerations of violaceous borders in lower limbs and/or trunk. PG treatment varies according to the severity of the lesion and may either respond to local therapies or require immunosuppressive agents. In this article, we present the case of an antiphospholipid antibody-positive 59-year-old female patient diagnosed with granulomatosis with polyangiitis who developed severe PG-like skin involvement that was responsive to rituximab therapy.
坏疽性脓皮病(PG)是一种嗜中性皮肤病,最常表现为下肢和/或躯干出现边界呈紫罗兰色的疼痛性溃疡。PG的治疗根据病变的严重程度而有所不同,可能对局部治疗有反应,也可能需要使用免疫抑制剂。在本文中,我们报告了一例抗磷脂抗体阳性的59岁女性患者,该患者被诊断为肉芽肿性多血管炎,出现了严重的类似PG的皮肤病变,对利妥昔单抗治疗有反应。