Life-threatening purpura and vasculitis

被引:2
|
作者
Katsambas, A [1 ]
Stefanaki, C [1 ]
机构
[1] Univ Athens, Andreas Sygros Hosp, Dept Dermatol, Athens 11625, Greece
关键词
D O I
10.1016/j.clindermatol.2004.06.002
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Palpable purpura, the inflammation of blood vessels is the hallmark of vasculitis. It can be observed in a variety of settings, where vessels can be affected primarily or as a secondary event. Every patient with vasculitis should be considered to have a systemic disease unless proven otherwise. One or more systemic symptoms occur in at least 50% of patients and there is no way to predict systemic involvement. Patients may demonstrate mild systemic involvement like arthralgia and arthritis, fever and malaise or more severe symptoms such as massive proteinuria and raised creatinine leading to chronic renal failure, severe intestinal bleeding or perforation with a fatal outcome. In this article we will review the life-threatening aspects of purpura and vasculitis. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:227 / 237
页数:11
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