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Could it be Henoch-Schonlein purpura?
被引:0
作者:
Lim, Danforn C. E.
[1
]
Cheng, Lisa N. C.
[2
]
Wong, Felix W. S.
[1
]
机构:
[1] Univ Notre Dame, Sch Med, Sydney, NSW, Australia
[2] Univ New S Wales, Sydney Childrens Hosp, Sydney, NSW 2052, Australia
关键词:
RHEUMATOLOGY;
1990;
CRITERIA;
CHILDHOOD;
CHILDREN;
MANIFESTATIONS;
CLASSIFICATION;
VASCULITIS;
IGA;
D O I:
暂无
中图分类号:
R1 [预防医学、卫生学];
学科分类号:
1004 ;
120402 ;
摘要:
Background Henoch-Schonlein purpura is the most common form of systemic vasculitis in the paediatric setting with 90% of cases occuring in childhood. Although diagnosis in the primary care setting may be difficult, it is vital in order to avoid significant complications. Objective This article outlines the pathogenesis, clinical manifestations and classification of Henoch-Schonlein purpura and details evidence based investigations and management. Discussion Henoch-Schonlein purpura is a self limiting disease characterised by a tetrad of clinical manifestations that vary in occurrence and order of presentation. There is no single diagnostic test to confirm Henoch-Schonlein purpura; diagnosis depends on recognition of clinical manifestations. Management usually occurs in the ambulatory setting and is mainly supportive. Priorities include symptom relief and preventive therapy to reduce the risk of complications. Further trials to clarify the role of glucocorticosteroids are needed before a definitive role for steroids in the management of Henoch-Schonlein purpura can be established.
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页码:321 / 324
页数:4
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