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Comparison of High-Dose Corticosteroid Pulse Therapy and Combination Therapy Using Oral Cyclosporine with Low-Dose Corticosteroid in Severe Alopecia Areataopen access

Authors
Yeo, In KwonKo, Bun JungNo, Yeon A.Lim, Ee SeokPark, Kui YoungLi, KapsokKim, Beom JoonSeo, Seoiag JunKim, Myeung NamHong, Chang Kwun
Issue Date
Dec-2015
Publisher
KOREAN DERMATOLOGICAL ASSOC
Keywords
Alopecia areata; Cyclosporine; Pulse therapy
Citation
ANNALS OF DERMATOLOGY, v.27, no.6, pp 676 - 681
Pages
6
Journal Title
ANNALS OF DERMATOLOGY
Volume
27
Number
6
Start Page
676
End Page
681
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/8885
DOI
10.5021/ad.2015.27.6.676
ISSN
1013-9087
2005-3894
Abstract
Background: Severe alopecia areata (AA) is resistant to conventional treatment. Although systemic oral,corticosteroids are an effective treatment for patients with severe AA, those drugs have many adverse effects. Corticosteroid pulse therapy has been introduced to increase therapeutic effects and reduce adverse effects. However, the treatment modality in severe AA is still controversial. Objective: To evaluate the effectiveness of corticosteroid pulse therapy in patients with severe AA compared with treatment with oral cyclosporine with corticosteroid. Methods: A total of 82 patients with severe AA were treated with corticosteroid pulse therapy, and 60 patients were treated with oral cyclosporine with corticosteroid. Both groups were retrospectively evaluated for therapeutic efficacy according to AA type and disease duration. Results: In 82 patients treated with corticosteroid pulse therapy, 53 (64.6%) were good responders (>50% hair regrowth). Patients with the plurifocal (PF) type of AA and those with a short disease duration (<= 3 months) showed better responses. In 60 patients treated with oral cyclosporine with corticosteroid, 30 (50.0%) patients showed a good response. The AA type or disease duration, however, did not significantly affect the response to treatment. Conclusion: Corticosteroid pulse therapy may be a better treatment option than combination therapy in severe AA patients with the PF type.
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