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抗磷脂抗体与缺血性中风。

Antiphospholipid antibodies and ischemic stroke.

作者信息

Brey R L

机构信息

Division of Neurology, University of Texas Health Science Center, San Antonio 78284-7883.

出版信息

Heart Dis Stroke. 1992 Nov-Dec;1(6):379-82.

PMID:1344135
Abstract

Antibodies directed against phospholipids are highly associated with episodes of venous and arterial thrombosis, which are often recurrent. There seems to be a skewed frequency of cerebral thrombosis when the arterial circulation is affected. Clinical clues that should lead to evaluation for aPL include stroke in a young adult, recurrent thrombosis or miscarriage, and thrombocytopenia. Associated laboratory abnormalities include a biologically false-positive test for syphilis, abnormal antinuclear antibody titers, and a high erythrocyte sedimentation rate. If the activated partial thromboplastin time is prolonged on routine screening and does not correct with mixing studies, a lupus anticoagulant should be suspected. However, more sensitive and specific tests are usually necessary to detect aPL. Many in vitro and more recently in vivo systems strongly suggest that aPL may be directly implicated in the pathogenesis of thrombosis. Optimal management of patients with aPL-associated thrombosis is unknown. The use of aggressive therapeutic management schemes with such agents as warfarin or corticosteroids is sometimes required.

摘要

针对磷脂的抗体与静脉和动脉血栓形成事件高度相关,这些血栓形成事件往往会复发。当动脉循环受到影响时,似乎脑血栓形成的频率存在偏差。提示应评估抗磷脂抗体(aPL)的临床线索包括年轻成年人的中风、复发性血栓形成或流产以及血小板减少症。相关的实验室异常包括梅毒生物学假阳性试验、抗核抗体滴度异常以及红细胞沉降率升高。如果在常规筛查中活化部分凝血活酶时间延长且在混合试验中未纠正,则应怀疑存在狼疮抗凝物。然而,通常需要更敏感和特异的检测来检测aPL。许多体外以及最近的体内系统强烈表明,aPL可能直接参与血栓形成的发病机制。aPL相关血栓形成患者的最佳管理方法尚不清楚。有时需要使用华法林或皮质类固醇等药物进行积极的治疗管理方案。

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