CYCLOPHOSPHAMIDE THERAPY OF SEVERE SYSTEMIC NECROTIZING VASCULITIS

被引:510
作者
FAUCI, AS
KATZ, P
HAYNES, BF
WOLFF, SM
机构
[1] Clinical Physiology Section, Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, MD
关键词
D O I
10.1056/NEJM197908023010503
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We studied 17 patients with severe systemic necrotizing vasculitis over an 11-year-period. Sixteen patients were treated daily with cyclophosphamide (2 mg per kilogram per day), and one was treated with azathioprine (2 mg per kilogram per day). Before entering the study, all patients had active and progressive disease, even though 16 patients had been receiving corticosteroids that had caused severe and often incapacitating toxic side effects. Three patients died during the study. Complete and often dramatic remissions occurred in the surviving 14 patients, who were then placed on alternate-day corticosteroid treatment with continuation of cyclophosphamide. Corticosteroids were later discontinued in seven patients. The mean duration of remission was 22 months (range, two to 61). No patient showed recurrence of disease during treatment with cytotoxic agents. (N Engl J Med 301:235–238, 1979) THE term vasculitis denotes inflammation and necrosis of blood vessels. The process may be the primary manifestation of several clinical syndromes or it may be a relatively minor feature of other primary diseases. The heterogeneous group of disorders within the broad spectrum of vasculitis have been recently re-categorized and their interrelations delineated.1 The vasculitic syndromes show a wide range of severity. Some, such as the hypersensitivity vasculitides generally limited to the skin, are relatively less severe and rarely life threatening. On the other hand, systemic necrotizing vasculitis consists of a group of disorders characterized by severe disseminated necrotizing vasculitis of. © 1979, Massachusetts Medical Society. All rights reserved.
引用
收藏
页码:235 / 238
页数:4
相关论文
共 17 条
[1]  
CHURG J, 1951, AM J PATHOL, V27, P277
[2]   GRANULOMATOUS VASCULITIDES - DISTINCT BUT RELATED [J].
FAUCI, AS .
ANNALS OF INTERNAL MEDICINE, 1977, 87 (06) :782-783
[3]   WEGENERS GRANULOMATOSIS - STUDIES IN 18 PATIENTS AND A REVIEW OF LITERATURE [J].
FAUCI, AS ;
WOLFF, SM .
MEDICINE, 1973, 52 (06) :535-561
[4]   CYCLOPHOSPHAMIDE-INDUCED REMISSIONS IN ADVANCED POLYARTERITIS NODOSA [J].
FAUCI, AS ;
DOPPMAN, JL ;
WOLFF, SM .
AMERICAN JOURNAL OF MEDICINE, 1978, 64 (05) :890-894
[5]   SPECTRUM OF VASCULITIS - CLINICAL, PATHOLOGIC, IMMUNOLOGICAL, AND THERAPEUTIC CONSIDERATIONS [J].
FAUCI, AS ;
HAYNES, BF ;
KATZ, P .
ANNALS OF INTERNAL MEDICINE, 1978, 89 (05) :660-676
[6]   LONG-TERM FOLLOW-UP STUDY OF PERIARTERITIS NODOSA [J].
FROHNERT, PP ;
SHEPS, SG .
AMERICAN JOURNAL OF MEDICINE, 1967, 43 (01) :8-&
[7]   REGRESSION OF CORONARY-ARTERY ANEURYSMS IN INFANTILE POLYARTERITIS NODOSA [J].
GLANZ, S ;
BITTNER, SJ ;
BERMAN, MA ;
DOLAN, TF ;
TALNER, NS .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 294 (17) :939-941
[8]   PERIARTERITIS NODOSA - REMISSION ACHIEVED WITH COMBINED PREDNISONE AND AZATHIOPRINE THERAPY [J].
MELAM, H ;
PATTERSON, R .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1971, 121 (05) :424-+
[9]   POLYARTERITIS IN CHILDREN [J].
REIMOLD, EW ;
WEINBERG, AG ;
FINK, CW ;
BATTLES, ND .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1976, 130 (05) :534-541
[10]   WEGENERS GRANULOMATOSIS - LONG-TERM FOLLOWUP OF PATIENTS TREATED WITH CYCLOPHOSPHAMIDE [J].
REZA, MJ ;
DORNFELD, L ;
GOLDBERG, LS ;
BLUESTONE, R ;
PEARSON, CM .
ARTHRITIS AND RHEUMATISM, 1975, 18 (05) :501-506