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Sir, We read with interest the report...


European Journal of Dermatology. Volume 12, Number 4, 387-8, July - August 2002, Lettre de l'éditeur



Author(s) : S.L. WALKER, B. KIRBY, R.J.G. CHALMERS, Dermatology Centre, University of Manchester Medical School, Hope Hospital, Manchester, UK, M6 8HD..

ARTICLE

Sir,

We read with interest the report by Yosahimasu and colleagues of the use of 0.1% tacrolimus ointment in patients with various forms of lupus erythematosus [1]. In contrast to their experience in patients with chronic discoid lupus erythematosus (CDLE), we have recently had success in treating two patients with severe recalcitrant CDLE with a compound preparation of 0.3% tacrolimus in 0.05% clobetasol propionate ointment. The details of these cases will shortly be published in the British Journal of Dermatology but are described here in brief. A 54-year-old woman with systemic lupus erythematosus and recalcitrant CDLE (Fig. 1) who had failed to respond to antimalarials, thalidomide and very potent topical corticosteroids was treated with 0.3% tacrolimus in 0.05% clobetasol propionate. A dramatic improvement was noted within 10 days and has been maintained over a period of six months (Fig. 2). A similar response to this novel therapy has also been achieved in a 52-year-old woman whose CDLE was not controlled by a combination of very potent topical corticosteroids, hydroxychloroquine, mepacrine and prednisolone.

Because 0.3% tacrolimus in 0.05% clobetasol propionate has been used successfully in our department to manage pyoderma gangrenosum [2], we chose to use this preparation in two patients who had failed to respond to other measures including potent topical corticosteroids. None of three patients with CDLE treated by Yoshimasu's group with 0.1% tacrolimus ointment showed any improvement; one patient with erythematous lupus and all three with systemic lupus did improve. The authors suggest that low absorption or unresponsiveness of target cells may be responsible. We would like to suggest that the former explanation may be correct and that the tissue concentrations achieved with the 0.1% ointment may have been sufficient for patients with less infiltrated forms of cutaneous lupus but inadequate in those with chronic discoid plaques. It is also possible that the combination of tacrolimus with corticosteroids had an additive or even synergistic effect. More formal studies are now required to confirm the place of topical tacrolimus in the management of cutaneous lupus but these initial experiences suggest that it may prove to have significant advantages over current therapy options.

References

1. Yoshimasu T, Ohtani T, Oshima A, et al. Topical FK506 (tracrolimus) therapy for facial erythematous lesions of cutaneous lupus erythematosus and dermatomyositis. Eur J Dermatol 2002; 12: 50-2.

2. Lyon CC, Smith AJ, Beck MH, et al. Parastomal pyoderma gangrenosus: clinical features and management. J Am Acad Dermatol 2000; 42: 992-1002.

   

   
    


 

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