Center for Dermatology Research, Department of Dermatology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Department of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Int J Dermatol. 2021 Dec;60(12):e486-e492. doi: 10.1111/ijd.15539. Epub 2021 Mar 19.
Pyoderma gangrenosum is a rare neutrophilic dermatosis that is commonly treated with systemic corticosteroids; however, their potent side effects may warrant tapering, and non-steroidal systemic immunosuppressants may help maintain or bolster disease clearance during weaning. Although cyclosporine is regarded as a favorable corticosteroid-sparing agent, it is associated with several side effects, such as renal toxicity and hypertension, that may limit its feasibility. Mycophenolate mofetil is a well-tolerated alternative with limited data. Institutional review board approval was obtained to review patients from a single institution who received mycophenolate mofetil for pyoderma gangrenosum between January 1, 2010, and December 31, 2019. A systematic MEDLINE (PubMed) review was performed of articles containing linked keywords: "mycophenolate mofetil" and "pyoderma gangrenosum". Patient demographics, presentation details, and treatment regimen characteristics were recorded. Fourteen of our pyoderma gangrenosum patients were treated with mycophenolate mofetil concomitantly with prednisone. Ninety-three percent of our patients achieved improvement within 12 months (mean 4.5 months), including five patients who experienced complete healing. Outcomes in literature patients were comparable; 77% either improved or maintained clearance with mycophenolate mofetil. Greater than 80% of total patients experienced healing or adequate disease control at a median dose of 2000 mg daily. The most common side effects of mycophenolate mofetil were myelosuppression and gastrointestinal upset, which were both seen in 18% of patients. Although this study is subject to publication bias, mycophenolate mofetil appears to be an efficacious and well-tolerated adjunctive therapy option for pyoderma gangrenosum.
坏疽性脓皮病是一种罕见的中性粒细胞皮肤病,通常用全身性皮质类固醇治疗;然而,它们的强大副作用可能需要逐渐减少,非甾体类全身性免疫抑制剂可能有助于在停药期间维持或加强疾病清除。环孢素被认为是一种有利的皮质类固醇节约剂,但它与几种副作用有关,如肾毒性和高血压,这可能限制了它的可行性。霉酚酸酯是一种耐受性良好的替代药物,但数据有限。获得机构审查委员会的批准,审查了 2010 年 1 月 1 日至 2019 年 12 月 31 日期间在一家机构接受霉酚酸酯治疗坏疽性脓皮病的患者。对包含链接关键字的文章进行了系统的 MEDLINE(PubMed)综述:“霉酚酸酯”和“坏疽性脓皮病”。记录了患者的人口统计学、表现细节和治疗方案特征。我们的 14 例坏疽性脓皮病患者同时接受霉酚酸酯和泼尼松治疗。93%的患者在 12 个月内(平均 4.5 个月)得到改善,包括 5 例完全治愈的患者。文献中的患者结局相当;77%的患者用霉酚酸酯改善或维持清除率。超过 80%的患者在中位剂量为 2000mg/天的情况下,获得愈合或充分的疾病控制。霉酚酸酯最常见的副作用是骨髓抑制和胃肠道不适,这两种副作用在 18%的患者中都有发生。尽管这项研究存在发表偏倚,但霉酚酸酯似乎是一种有效的、耐受性良好的坏疽性脓皮病辅助治疗选择。