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抗磷脂综合征:一种复杂多系统疾病的全面综述

Antiphospholipid syndrome: a comprehensive review of a complex and multisystemic disease.

作者信息

Palomo I, Segovia F, Ortega C, Pierangeli S

机构信息

Department of Biochemistry and Immunohematology, School of Health Sciences, University of Talca, Talca, Chile.

出版信息

Clin Exp Rheumatol. 2009 Jul-Aug;27(4):668-77.

Abstract

The antiphospholipid syndrome (APS) is an acquired thombophilia, which is characterized by one or more thrombotic episodes and obstetric complications in the presence of antiphospholipid (aPL) antibodies (Abs). APL Abs are detected by laboratory tests such as lupus anticoagulant (LAC), anticardiolipin (aCL) and anti-Beta2-glycoprotein I (Beta2GPI) Abs. This article reviews the most current aspects of APS with emphasis on the pathophysiology of the disease, clinical manifestations, laboratory tests, and current modalities of treatment.

摘要

抗磷脂综合征(APS)是一种获得性血栓形成倾向疾病,其特征为在存在抗磷脂(aPL)抗体(Abs)的情况下发生一次或多次血栓形成事件及产科并发症。aPL抗体通过实验室检测来发现,如狼疮抗凝物(LAC)、抗心磷脂(aCL)和抗β2糖蛋白I(β2GPI)抗体。本文综述了APS的最新情况,重点关注该疾病的病理生理学、临床表现、实验室检测及当前的治疗方式。

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