TREATMENT OF DERMATOMYOSITIS WITH INTRAVENOUS GAMMA-GLOBULIN

被引:162
作者
LANG, BA
LAXER, RM
MURPHY, G
SILVERMAN, ED
ROIFMAN, CM
机构
[1] HOSP SICK CHILDREN,DEPT PEDIAT,DIV IMMUNOL ALLERGY,555 UNIV AVE,TORONTO M5G 1X8,ONTARIO,CANADA
[2] HOSP SICK CHILDREN,DEPT PEDIAT,DIV NEUROL,TORONTO M5G 1X8,ONTARIO,CANADA
[3] DALHOUSIE UNIV,IZAAK WALTON KILLAM HOSP CHILDREN,DEPT PEDIAT,HALIFAX B3J 3G9,NS,CANADA
[4] HOSP SICK CHILDREN,DEPT PEDIAT,DIV RHEUMATOL,TORONTO M5G 1X8,ONTARIO,CANADA
关键词
D O I
10.1016/0002-9343(91)90010-U
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PURPOSE: The mainstay of pharmacologic therapy in patients with dermatomyositis is corticosteroids. However, because patients sometimes become refractory to these drugs and because these drugs have potential short- and long-term toxicities, alternate therapy is highly desirable. Therefore, a pilot study was initiated using high-dose intravenous gammaglobulin (IVGG) in the treatment of dermatomyositis. PATIENTS AND METHODS: IVGG was administered to five patients with juvenile dermatomyositis. Prior to IVGG treatment, all patients had persistent muscle weakness despite daily corticosteroids and three patients had developed unacceptable steroid toxicity. Two of the patients had previously developed toxicity while receiving immunosuppressive therapy. RESULTS: IVGG therapy resulted in improved muscle strength and ameliorated skin rash in all patients. The percentage increase in muscle strength as measured by sphygmomanometry following the 9-month course of IVGG ranged from 56% to 606% in the proximal lower extremities and from 30% to 186% in the proximal upper extremities. Following IVGG therapy, prednisone could be discontinued or the dose reduced in all patients. CONCLUSION: This study suggests that IVGG may allow steroid sparing in dermatomyositis and may provide a safe alternative to cytotoxic therapy.
引用
收藏
页码:169 / 172
页数:4
相关论文
共 17 条
[1]   DERMATOMYOSITIS (SYSTEMIC ANGIOPATHY) OF CHILDHOOD [J].
BANKER, BQ ;
VICTOR, M .
MEDICINE, 1966, 45 (04) :261-+
[2]   POLYMYOSITIS AND DERMATOMYOSITIS .1. [J].
BOHAN, A ;
PETER, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (07) :344-347
[3]  
BOWLES NE, 1987, LANCET, V1, P1004
[4]   TREATMENT OF DERMATOMYOSITIS IN CHILDHOOD [J].
DUBOWITZ, V .
ARCHIVES OF DISEASE IN CHILDHOOD, 1976, 51 (07) :494-500
[5]  
GAJDOS P, 1984, LANCET, V1, P406
[6]   CYCLOSPORINE IN JUVENILE DERMATOMYOSITIS [J].
HECKMATT, J ;
SAUNDERS, C ;
PETERS, AM ;
ROSE, M ;
HASSON, N ;
THOMPSON, N ;
CAMBRIDGE, G ;
HYDE, SA ;
DUBOWITZ, V .
LANCET, 1989, 1 (8646) :1063-1066
[7]  
JACOBS JC, 1977, PEDIATRICS, V59, P212
[8]   THE TREATMENT OF KAWASAKI SYNDROME WITH INTRAVENOUS GAMMA-GLOBULIN [J].
NEWBURGER, JW ;
TAKAHASHI, M ;
BURNS, JC ;
BEISER, AS ;
CHUNG, KJ ;
DUFFY, CE ;
GLODE, MP ;
MASON, WH ;
REDDY, V ;
SANDERS, SP ;
SHULMAN, ST ;
WIGGINS, JW ;
HICKS, RV ;
FULTON, DR ;
LEWIS, AB ;
LEUNG, DYM ;
COLTON, T ;
ROSEN, FS ;
MELISH, ME .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (06) :341-347
[9]   IMMUNOSUPPRESSIVE AGENTS IN CORTICOSTEROID-REFRACTORY CHILDHOOD DERMATOMYOSITIS [J].
NIAKAN, E ;
PITNER, SE ;
WHITAKER, JN ;
BERTORINI, TE .
NEUROLOGY, 1980, 30 (03) :286-291
[10]   REVERSAL OF CHRONIC POLYMYOSITIS FOLLOWING INTRAVENOUS IMMUNE SERUM GLOBULIN THERAPY [J].
ROIFMAN, CM ;
SCHAFFER, FM ;
WACHSMUTH, SE ;
MURPHY, G ;
GELFAND, EW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1987, 258 (04) :513-515