Urticarial vasculitis

被引:26
|
作者
Chang, Suyoung [1 ]
Carr, Warner [1 ]
机构
[1] Walter Reed Army Med Ctr, Washington, DC 20307 USA
关键词
cutaneous; hypocomplementemic; leukocytoclastic; urticaria; vasculitis;
D O I
10.2500/aap.2007.28.2972
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
A case of urticarial vasculitis (UV) is presented. The pathogenesis, clinical characteristics, diagnosis, and management of this disease arc reviewed, followed by clinical pearls and pitfalls for the practicing allergist (Venzor J, et al., Urticarial vasculitis, Clin Rev Allergy Immunol 23:201-216, 2002). The lesions in UV typically lasts > 24 hours in a fixed location, resolves with residual hyperpigmentation, and may or may not be pruritic. In contrast, standard urticaria lesions persist < 24 hours, leave no trace, and is always pruritic (Black AK, Urticarial vasculitis, Clin Dermatol 17:565-569, 1999). Since urticarial vasculitis is characterized by a variety of cutaneous, systemic, and serological features, different names of this disorder exist in the literature (Wisnieski JJ, Urticarial vasculitis, Curr Opin Rheumatol 12:24-31, 2000). A biopsy of an active lesion remains the gold standard for the diagnosis of urticarial vasculitis.
引用
收藏
页码:97 / 100
页数:4
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