Vascular manifestations of systemic lupus erythematosis

被引:0
|
作者
Radic, M. [1 ]
Kaliterna, D. Martinovic [1 ]
Radic, J. [2 ]
机构
[1] Univ Split, Sch Med, Univ Hosp Ctr Split, Div Rheumatol & Clin Immunol, Split, Croatia
[2] Univ Split, Sch Med, Univ Hosp Ctr Split, Div Nephrol, Split, Croatia
来源
NETHERLANDS JOURNAL OF MEDICINE | 2013年 / 71卷 / 01期
关键词
Systemic lupus erythematosus; vasculitis; vasculopathy; antiphospholipid syndrome; INTERNATIONAL CONSENSUS STATEMENT; CATASTROPHIC ANTIPHOSPHOLIPID SYNDROME; LIVEDOID VASCULOPATHY; CLASSIFICATION CRITERIA; MYCOPHENOLATE-MOFETIL; RECURRENT THROMBOSIS; CUTANEOUS-VASCULITIS; RISK-FACTORS; ANTICARDIOLIPIN ANTIBODIES; UPDATE;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Systemic lupus erythematosus (SLE) is an autoimmune connective disease, where vascular lesions are one of the typical symptoms. The differentiation of the type of vascular complications in SLE is very difficult, sometimes impossible, and requires an in-depth immune and histopathological approach, and extensive clinical experience. It may play a key role in the choice of treatment strategy and prediction of patient prognosis. SLE is a prototype of a multisystem autoimmune connective tissue disease, marked by immune complex-mediated lesions of blood vessels in diverse organs. Therefore, awareness of the aetiology, pathophysiology, the clinical and histopathogical setting, and SLE-associated vascular complications is of great clinical significance. In this review, the spectrum of vascular abnormalities and the options currently available to treat the vascular manifestations of SLE are discussed.
引用
收藏
页码:10 / 16
页数:7
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