VITILIGO. TREATMENT OF 12 CASES WITH TOPICAL TACROLIMUS

被引:8
作者
Almeida, Pablo [1 ]
Borrego, Leopoldo [1 ]
Rodriguez-Lopez, Julio [1 ]
Lujan, Dunia [1 ]
Cameselle, Daniel [1 ]
Hernandez, Buenaventura [1 ]
机构
[1] Hosp Univ Insular Gran Canaria, Serv Dermatol, Avda Maritima Sur,S-N, E-36016 Las Palmas Gran Canaria, Spain
来源
ACTAS DERMO-SIFILIOGRAFICAS | 2005年 / 96卷 / 03期
关键词
vitiligo; tacrolimus; dyschromia; hypopigmentation; topical treatment;
D O I
10.1016/S0001-7310(05)73058-1
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction. Vitiligo is a frequent dyschromia, characterized by achromic macules that reflect the absence of melanocytes. The cause of this selective destruction seems to be due to an autoimmune phenomenon. Tacrolimus is an immunomodulator produced by Streptomyces tsukubaensis, whose topical use has been approved for atopic dermatitis. It has been tested in other dermatoses where immunological phenomena are involved. Material and methods. During the period from September 1, 2003 to April 30, 2004, an open study was carried out on 12 cases of vitiligo treated with topical tacrolimus 0.1 % twice a day. The degree of repigmentation was analyzed using digital photography at the initial visit, and at three and six months. The response in each case was taken into consideration, as well as the response by treated area. Possible adverse effects during the treatment period were also noted. Results. 50 % of the patients treated showed repigmentation with good (50 %-75 %) or excellent (> 75%) improvement after 6 months. All of the patients with facial involvement achieved repigmentation of over 50 % in this location. Repigmentation in all cases took place homogeneously and centripetally, rather than in a perifollicular pattern. Repigmentation began before three months of treatment had elapsed in 10 patients, and after three months in the remaining two. We did not find any evidence of adverse effects except pruritus in the eyelid area in two patients during the first week of treatment. Conclusion. We believe that tacrolimus 0.1 % applied topically for a minimum of six months may be a valid alternative in the treatment of vitiligo in the facial area, especially the eyelids, where other therapeutic modes are not recommended because of the possible side effects.
引用
收藏
页码:159 / 163
页数:5
相关论文
共 13 条
[1]   Repigmentation of chronic vitiligo lesions by following tacrolimus plus ultraviolet-B-narrow-band [J].
Castanedo-Cazares, JP ;
Lepe, V ;
Moncada, B .
PHOTODERMATOLOGY PHOTOIMMUNOLOGY & PHOTOMEDICINE, 2003, 19 (01) :35-36
[2]   Surgical treatment of vitiligo: why, when and how [J].
Falabella, R .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2003, 17 (05) :518-520
[3]   Topical tacrolimus for repigmentation of vitiligo [J].
Grimes, PE ;
Soriano, T ;
Dytoc, MT .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2002, 47 (05) :789-791
[4]   Tacrolimus: a review of its use for the management of dermatoses [J].
Gupta, AK ;
Adamiak, A ;
Chow, M .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2002, 16 (02) :100-114
[5]   Autoimmune aspects of vitiligo [J].
Kemp, EH ;
Waterman, EA ;
Weetman, AP .
AUTOIMMUNITY, 2001, 34 (01) :65-77
[6]   COMPARISON OF 0.05-PERCENT CLOBETASOL PROPIONATE CREAM AND TOPICAL PUVASOL IN CHILDHOOD VITILIGO [J].
KHALID, M ;
MUJTABA, G ;
HAROON, TS .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1995, 34 (03) :203-205
[7]   Vitiligo [J].
Kovacs, SO .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1998, 38 (05) :647-666
[8]   A double-blind randomized trial of 0.1% tacrolimus vs 0.05% clobetasol for the treatment of childhood vitiligo [J].
Lepe, V ;
Moncada, B ;
Castanedo-Cazares, JP ;
Torres-Alvarez, MB ;
Ortiz, CA ;
Torres-Rubalcava, AB .
ARCHIVES OF DERMATOLOGY, 2003, 139 (05) :581-585
[9]   Topical application of the immunosuppressant tacrolimus accelerates carcinogenesis in mouse skin [J].
Niwa, Y ;
Terashima, T ;
Sumi, H .
BRITISH JOURNAL OF DERMATOLOGY, 2003, 149 (05) :960-967
[10]   Nonsurgical repigmentation therapies in vitiligo - Meta-analysis of the literature [J].
Njoo, MD ;
Spuls, PI ;
Bos, JD ;
Westerhof, W ;
Bossuyt, PMM .
ARCHIVES OF DERMATOLOGY, 1998, 134 (12) :1532-1540