UVA1 phototherapy for treatment of necrobiosis lipoidica

被引:31
作者
Beattie, PE [1 ]
Dawe, RS [1 ]
Ibbotson, SH [1 ]
Ferguson, J [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Dept Dermatol, Photobiol Unit, Dundee, Scotland
关键词
D O I
10.1111/j.1365-2230.2005.02059.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The primary cause of collagen degeneration in necrobiosis lipoidica (NL) is proposed to be immunologically mediated vascular disease. Ultraviolet (UV)A1 has been used successfully to treat scleroderma in which both vascular damage and collagen dysregulation also occur. We treated six patients with NL [(five women; mean age of 32 years (range 22-70) and mean disease duration of 2.9 years (range 6 months to 5 years)] with a high-output ultraviolet (UV)A1 2-kW filtered metal halide source (Dr Honle; Dermalight ultrA 1) having an emission spectrum of 340-440 nm. All patients had NL on the shins, which had been unresponsive to potent topical corticosteroid therapy (n = 6) and had responded minimally or not at all to TL-01 UVB (n = 2), topical psoralen plus UVA (PUVA) soaking (n = 2) or oral PUVA (n = 1) therapy. Patients received a variable number of total exposures (15-51), given 3-5 times weekly. NL resolved completely in one patient; this patient had minimal improvement after the first course of 16 exposures, but after a further 13 exposures, resolution occurred 6 months later. Two subjects obtained moderate improvement in their overall disease severity after 15 and 24 exposures, while two had only minimal improvement after 15 and 51 exposures. The remaining patient had no improvement after 16 treatments. Patients with the shortest disease duration had the greatest response. UVA1 therapy may be of benefit for the treatment of NL as an adjuvant therapy to topical corticosteroids or as a second-line alternative to other phototherapies, and may have a superior outcome in a proportion of patients.
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页码:235 / 238
页数:4
相关论文
共 13 条
[1]   Dose-response and time-course characteristics of UV-A1 erythema [J].
Beattie, PE ;
Dawe, RS ;
Ferguson, J ;
Ibbotson, SH .
ARCHIVES OF DERMATOLOGY, 2005, 141 (12) :1549-1555
[2]  
Breuckmann Frank, 2002, BMC Dermatol, V2, P12, DOI 10.1186/1471-5945-2-12
[3]   Treatment of necrobiosis lipoidica with topical psoralen plus ultraviolet A [J].
De Rie, MA ;
Sommer, A ;
Hoekzema, R ;
Neumann, HAM .
BRITISH JOURNAL OF DERMATOLOGY, 2002, 147 (04) :743-747
[4]   High-dose ultraviolet A1 (UVA1), but not UVA/UVB therapy, decreases IgE-binding cells in lesional skin of patients with atopic eczema [J].
Grabbe, J ;
Welker, P ;
Humke, S ;
Grewe, M ;
Schopf, E ;
Henz, BM ;
Krutmann, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (03) :419-422
[5]   Successful ultraviolet A1 treatment of cutaneous sarcoidosis [J].
Graefe, T ;
Konrad, H ;
Barta, U ;
Wollina, U ;
Elsner, P .
BRITISH JOURNAL OF DERMATOLOGY, 2001, 145 (02) :354-355
[6]   Changes in collagen I and collagen III metabolism in patients with generalized atopic eczema undergoing medium-dose ultraviolet A1 phototherapy [J].
Mempel, M ;
Schmidt, T ;
Boeck, K ;
Brockow, K ;
Stachowitz, S ;
Fesq, H ;
Schäfer, T ;
Thomsen, S ;
Schnopp, C ;
Ring, J ;
Probst, R ;
Luppa, P ;
Abeck, D .
BRITISH JOURNAL OF DERMATOLOGY, 2000, 142 (03) :473-480
[7]   Phototherapy with UV-A-I for generalized granuloma annulare [J].
Muchenberger, S ;
Schopf, E ;
Simon, JC .
ARCHIVES OF DERMATOLOGY, 1997, 133 (12) :1605-1605
[8]   ULTRAVIOLET-A IRRADIATION STIMULATES COLLAGENASE PRODUCTION IN CULTURED HUMAN FIBROBLASTS [J].
PETERSEN, MJ ;
HANSEN, C ;
CRAIG, S .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (04) :440-444
[9]   THE CUTANEOUS IMMUNOPATHOLOGY OF NECROBIOSIS LIPOIDICA DIABETICORUM [J].
QUIMBY, SR ;
MULLER, SA ;
SCHROETER, AL .
ARCHIVES OF DERMATOLOGY, 1988, 124 (09) :1364-1371
[10]   Squamous cell carcinoma arising in long-standing necrobiosis lipoidica [J].
Santos-Juanes, J ;
Galache, C ;
Curto, JR ;
Carrasco, MP ;
Ribas, A ;
del Río, JS .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2004, 18 (02) :199-200