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白癜风、NB-UVB 和他克莫司:那不勒斯的经验。

Vitiligo, NB-UVB and tacrolimus: our experience in Naples.

机构信息

Section of Clinical, Allergological and Venerological Dermatology Department of Clinical Medicin and Surgery University of Naples Federico II, Naples, Italy -

出版信息

G Ital Dermatol Venereol. 2014 Feb;149(1):123-30.

PMID:24566573
Abstract

AIM

The aim of the present study was to evaluate the efficacy and safety of narrowband UVB (NB-UVB) compared with tacrolimus ointment 0.1% in patients with bilateral vitiligo.

METHODS

In this comparative study, four groups of patients were randomized. Each group was composed by 12 patients with bilateral vitiligo; in each group, every patient was irradiated with NB-UVB (length: 311 nm) twice a week for 9 months and applied tacrolimus ointment 0.1% twice a day on the other area in the same period. Before starting therapy and after 3, 6 and 9 months of therapy, a clinical and photographic evaluation of percentage of repigmentation was performed and Dermatology Life Quality Index Questionnaire was fulfilled.

RESULTS

A repigmentation at least partial occurred in 71% of patients after 36 weeks of treatment with tacrolimus ointment 0.1%; in the whole sample, 14 patients (29%) showed no repigmentation at all, with 2 of them discontinuing the therapy because of side effects (erythema and folliculitis-like manifestations). A homogeneous repigmentation at least partial occurred in 69% of patients after 36 weeks of treatment with NB-UVB; in the whole sample 15 patients (31%) showed no repigmentation at all, with 1 of them discontinuing the therapy because of side effects.

CONCLUSION

The present study confirmed that the efficacy of NB-UVB phototherapy in vitiligo is comparable to tacrolimus ointment 0.1% therapy. On the basis of our study, we may suggest tacrolimus ointment 0.1% as an alternative to NB-UVB therapy for treating vitiligo.

摘要

目的

本研究旨在评估窄谱中波紫外线(NB-UVB)与他克莫司软膏 0.1%在双侧白癜风患者中的疗效和安全性。

方法

在这项比较研究中,将四组患者随机分组。每组由 12 例双侧白癜风患者组成;在每组中,每位患者在同一时期每周接受 NB-UVB(波长:311nm)照射两次,同时在另一个区域每天涂抹他克莫司软膏 0.1%两次。在开始治疗前以及治疗 3、6 和 9 个月后,对患者进行临床和照片评估,以评估复色百分比,并填写皮肤病生活质量指数问卷。

结果

在使用他克莫司软膏 0.1%治疗 36 周后,有 71%的患者出现至少部分复色;在整个样本中,有 14 名患者(29%)完全没有复色,其中 2 名患者因不良反应(红斑和类似毛囊炎的表现)而停止治疗。在使用 NB-UVB 治疗 36 周后,有 69%的患者出现至少部分均匀复色;在整个样本中,有 15 名患者(31%)完全没有复色,其中 1 名患者因不良反应而停止治疗。

结论

本研究证实 NB-UVB 光疗在白癜风中的疗效与他克莫司软膏 0.1%治疗相当。基于我们的研究,我们可以建议他克莫司软膏 0.1%作为 NB-UVB 治疗的替代方法,用于治疗白癜风。

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