Pulsed high-dose corticosteroids combined with low-dose methotrexate in severe localized scleroderma

被引:130
作者
Kreuter, A [1 ]
Gambichler, T [1 ]
Breuckmann, F [1 ]
Rotterdam, S [1 ]
Freitag, M [1 ]
Stuecker, M [1 ]
Hoffmann, K [1 ]
Altmeyer, P [1 ]
机构
[1] Ruhr Univ Bochum, Dept Dermatol & Allergol, D-44791 Bochum, Germany
关键词
D O I
10.1001/archderm.141.7.847
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Objective: To evaluate the efficacy of pulsed high-dose corticosteroids combined with orally administered low-dose methotrexate therapy in patients with severe localized scleroderma (LS). Design: A prospective, nonrandomized, open pilot study Setting: Dermatology department at a university hospital in Bochum, Germany. Patients: Fifteen patients with histologically confirmed severe LS. Interventions: Oral methotrexate (15 mg/wk) combined with pulsed intravenous methylprednisolone (1000 mg for 3 days monthly) for at least 6 months. Main Outcome Measures: Treatment outcome was evaluated by means of a clinical score, 20-MHz ultrasonography, and histopathologic analysis. Safety assessment included the monitoring of adverse effects and clinical laboratory parameters. Results: One patient discontinued therapy. in most of the remaining 14 patients, significant elimination of all signs of active disease (inflammation) and remarkable softening of formerly affected sclerotic skin that resulted in a decrease of the mean +/- SD clinical score from 10.9 +/- 5.3 at the beginning to 5.5 +/- 2.5 at the end of therapy was observed (P <.001). Clinical improvement was confirmed by histologic and ultrasonographic assessments. No serious adverse effects were noted. Conclusions: These data suggest that pulsed high-dose corticosteroids combined with orally administered low-dose methotrexate therapy is beneficial and safe in the treatment of patients with LS. This treatment regimen should especially be considered for severe forms of LS in which conventional treatments have failed.
引用
收藏
页码:847 / 852
页数:6
相关论文
共 22 条
[1]
Topical calcipotriene for morphea linear scleroderma [J].
Cunningham, BB ;
Landells, IDR ;
Langman, C ;
Sailer, DE ;
Paller, AS .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1998, 39 (02) :211-215
[2]
Dutz J, 2000, Skin Therapy Lett, V5, P3
[3]
D-PENICILLAMINE IN THE TREATMENT OF LOCALIZED SCLERODERMA [J].
FALANGA, V ;
MEDSGER, TA .
ARCHIVES OF DERMATOLOGY, 1990, 126 (05) :609-612
[4]
Bone loss in patients treated with pulses of methylprednisolone is not negligible: a short term prospective observational study [J].
Haugeberg, G ;
Griffiths, B ;
Sokoll, KB ;
Emery, P .
ANNALS OF THE RHEUMATIC DISEASES, 2004, 63 (08) :940-944
[5]
Double-blind, placebo-controlled study of intralesional interferon gamma for the treatment of localized scleroderma [J].
Hunzelmann, N ;
Anders, S ;
Fierlbeck, G ;
Hein, R ;
Herrmann, K ;
Albrecht, M ;
Bell, S ;
Muche, R ;
WehnerCaroli, J ;
Gaus, W ;
Krieg, T .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 36 (03) :433-435
[6]
DEMONSTRATION OF INTERLEUKIN-2, INTERLEUKIN-4 AND INTERLEUKIN-6 IN SERA FROM PATIENTS WITH LOCALIZED SCLERODERMA [J].
IHN, H ;
SATO, S ;
FUJIMOTO, M ;
KIKUCHI, K ;
TAKEHARA, K .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1995, 287 (02) :193-197
[7]
DEMONSTRATION OF INTERLEUKIN-8 IN SERUM SAMPLES OF PATIENTS WITH LOCALIZED SCLERODERMA [J].
IHN, H ;
SATO, S ;
FUJIMOTO, M ;
KIKUCHI, K ;
TAKEHARA, K .
ARCHIVES OF DERMATOLOGY, 1994, 130 (10) :1327-1328
[8]
JOLY P, 1994, ARCH DERMATOL, V130, P664
[9]
TREATMENT OF LOCALIZED SCLERODERMA WITH PUVA BATH PHOTOCHEMOTHERAPY [J].
KERSCHER, M ;
VOLKENANDT, M ;
MEURER, M ;
LEHMANN, P ;
PLEWIG, G ;
ROCKEN, M .
LANCET, 1994, 343 (8907) :1233-1233
[10]
TREATMENT OF LOCALIZED SCLERODERMA BY UVA(1) PHOTOTHERAPY [J].
KERSCHER, M ;
DIRSCHKA, T ;
VOLKENANDT, M .
LANCET, 1995, 346 (8983) :1166-1166