Department of Dermatology, Howard University College of Medicine, Washington, DC 20060, USA.
G Ital Dermatol Venereol. 2010 Feb;145(1):57-78.
Despite much research done involving elucidation of the pathogenesis of vitiligo, a precise cause is still not known. Prevalent hypotheses include the autoimmune, genetic, neural, self-destruction, growth factor deficiency, viral, and convergence theories, which have served as the basis for treatment formulation. Topical therapies have been a mainstay of vitiligo treatment, with or without phototherapy. Topical treatments used in the treatment of vitiligo include steroids, calcineurin inhibitors, vitamin D analogues, pseudocatalase, and depigmenting agents. Combination therapies are used to improve the success rate of repigmentation. In this article, we have examined randomized controlled trials utilizing topical treatments used as monotherapy or combination therapy. Although psoralen and khellin can be used as topical agents, used in conjunction with UV radiation, we have not included them in the review due to their inability to be used as monotherapy. We have also excluded less used or ineffective topical agents, such as melagenina, topical phenylalanine, topical L-DOPA, coal tar, anacarcin forte oil and topical minoxidil. According to current guidelines, a less than two month trial of potent or very potent topical corticosteroids or topical calcineurin inhibitors may be used for therapy of localized vitiligo (<20% skin surface area). Combinations of topical corticosteroids with excimer laser and UVA seem to be more effective than steroids alone. Pseudocatalase plus NB-UVB does not seem to be more effective than placebo with NB-UVB. Combinations of vitamin D analogues have varied efficacy based on which type is used and the type of UV light. Efficacy of calcineurin inhibitor combinations also vary based on the type used and UV light combined, with tacrolimus being more effective with excimer laser. Pimecrolimus has been effective with NB-UVB and excimer laser on facial lesions, and microdermabrasion on localized areas.
尽管已经进行了大量研究来阐明白癜风的发病机制,但确切的原因仍不清楚。目前流行的假说包括自身免疫、遗传、神经、自我毁灭、生长因子缺乏、病毒和融合理论,这些假说为治疗方案的制定提供了依据。局部治疗一直是白癜风治疗的主要方法,无论是否联合光疗。用于治疗白癜风的局部治疗药物包括皮质类固醇、钙调神经磷酸酶抑制剂、维生素 D 类似物、假过氧化氢酶和脱色剂。联合治疗用于提高复色成功率。在本文中,我们检查了利用局部治疗药物进行单药或联合治疗的随机对照试验。虽然补骨脂素和花椒毒素可以作为局部药物与紫外线联合使用,但由于不能单独使用,我们没有将其包括在综述中。我们还排除了不太常用或无效的局部药物,如 melagenina、局部苯丙氨酸、局部 L-DOPA、煤焦油、anacarcin forte 油和局部米诺地尔。根据目前的指南,对于局限性白癜风(<20%皮肤表面积),可使用强效或超强效皮质类固醇或钙调神经磷酸酶抑制剂局部治疗,疗程少于两个月。局部皮质类固醇与准分子激光和 UVA 联合似乎比单独使用类固醇更有效。假过氧化氢酶加 NB-UVB 似乎不如 NB-UVB 加安慰剂有效。维生素 D 类似物的联合使用根据所使用的类型和紫外线的类型而疗效不同。钙调神经磷酸酶抑制剂联合使用的疗效也因所使用的类型和联合使用的紫外线而有所不同,他克莫司与准分子激光联合使用更有效。吡美莫司对 NB-UVB 和准分子激光治疗面部病变以及局部微磨皮有效。