Update in paediatric vasculitis

被引:8
作者
Ozen, Seza [2 ]
Fuhlbrigge, Robert C. [1 ]
机构
[1] Childrens Hosp Boston, Div Immunol, Program Pediat Rheumatol, Boston, MA 02115 USA
[2] Hacettepe Univ, Dept Pediat, Ankara, Turkey
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2009年 / 23卷 / 05期
关键词
paediatric rheumatology; vasculitis/classification; vasculitis/pathogenesis; vasculitis/diagnosis; polyarteritis nodosa; Wegener granulomatosis; microscopic polyangiitis; Henoch Schonlein purpura; Kawasaki disease; primary angiitis of the central nervous system; Takayasu arteritis; Churg-Strauss syndrome; anti-neutrophil cytoplasmic antibodies; HENOCH-SCHONLEIN PURPURA; ANTINEUTROPHIL CYTOPLASMIC AUTOANTIBODIES; LARGE-VESSEL VASCULITIS; ACUTE KAWASAKI-DISEASE; CHILDHOOD VASCULITIDES; EULAR RECOMMENDATIONS; POLYARTERITIS-NODOSA; FOLLOW-UP; CHILDREN; THERAPY;
D O I
10.1016/j.berh.2009.07.004
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Vasculitis refers to a heterogeneous group of disorders that are characterised by inflammatory destruction of blood vessels. Although simple to define, almost nothing about vasculitis is simple. From classification to diagnosis, and from pathogenesis to management, large gaps remain in Our understanding. Despite extensive and ongoing research, the fundamental mechanisms underlying the initiation and continuation of systemic vasculitis remain poorly understood. Thus, vasculitis continues to provide tremendous challenges to both clinicians and investigators and remains a rich source of issues for discussion. This review concentrates on recent changes proposed for the classification of paediatric vasculitis and advances in the concepts of aetiopathogenesis. Availability of improved classification criteria for children should prompt planning for multicentre-controlled studies for the treatment of these rare but important diseases. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:679 / 688
页数:10
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