Wang Lian, Li Xiao-Hua, Wen Xiang, Li Xiao-Xue, Du Dan, Li Yong, Jiang Xian
Department of Dermatology, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Exp Ther Med. 2020 Aug;20(2):1048-1052. doi: 10.3892/etm.2020.8740. Epub 2020 May 12.
Papulopustular rosacea (PPR) is characterized by central facial erythema and transient papules and/or pustules, with or without telangiectases. The treatment of PPR is challenging due to the unclear and complex pathogenesis. In the present retrospective study, patients with PPR treated with oral minocycline and supramolecular salicylic acid (SSA) 30% chemical peels enrolled between June 2018 and June 2019 were evaluated. All patients were treated with 50 mg minocycline twice a day and SSA 30% twice a month. A total of 19 patients were enrolled and all received the therapy for 12 weeks. A significant reduction of rosacea severity was observed by Investigator Severity Assessment (ISA) after treatment; the mean score reduced from 3.32±0.6 at baseline to 0.89±0.7 (P<0.01) at 12 weeks. After 12 weeks, all patients achieved at least a 'moderate response' and 17 patients (89.47%) obtained 'excellent improvement' in the Investigator Global Assessment of efficacy. No obvious adverse reactions were observed during each patient's visit. In conclusion, the combination treatment of minocycline and SSA 30% was an effective therapy for PPR. The limitation of the present study was that it was a retrospective analysis; more high-quality, prospective, blinded, controlled clinical trials are required to evaluate the efficacy based on the current study.
丘疹脓疱型玫瑰痤疮(PPR)的特征为面部中央红斑以及短暂性丘疹和/或脓疱,可伴有或不伴有毛细血管扩张。由于发病机制不明且复杂,PPR的治疗具有挑战性。在本回顾性研究中,对2018年6月至2019年6月期间接受口服米诺环素和30%超分子水杨酸(SSA)化学剥脱治疗的PPR患者进行了评估。所有患者均接受每日两次、每次50mg米诺环素以及每月两次30% SSA的治疗。共纳入19例患者,所有患者均接受了12周的治疗。治疗后,通过研究者严重程度评估(ISA)观察到玫瑰痤疮严重程度显著降低;平均评分从基线时的3.32±0.6降至12周时的0.89±0.7(P<0.01)。12周后,在研究者整体疗效评估中,所有患者至少达到“中度反应”,17例患者(89.47%)获得“显著改善”。在每位患者的就诊期间均未观察到明显不良反应。总之,米诺环素和30% SSA联合治疗是PPR的有效疗法。本研究的局限性在于它是一项回顾性分析;需要更多高质量、前瞻性、盲法、对照临床试验来基于当前研究评估疗效。