Antiphospholipid Syndrome (APS)

S. Berney
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Abstract

In 1983, Graham R V Hughes, MD published a 2-page article in the British Medical Journal entitled “Thrombosis, abortion, cerebral disease, and the lupus anticoagulant” [1]. This is generally acknowledged as the first report associating the antibodies subsequently named the antiphospholipid antibodies (aPL) with multiple clinical occurrences, now known as the Antiphospholipid Antibody Syndrome (or Hughes Syndrome). The aPL reflect a heterogeneous collection of antibodies which cause/contribute to the pathologic manifestations, as well as the “false positive Veneral Disease Research Laboratory (VDRL)” test and the misnomer “lupus anticoagulant”. Since that initial publication, many groups have expounded upon Dr. Hughes’ observation leading to 14 International Congresses on aPL. During these meetings, clinical and research observations were presented and discussed and diagnostic criteria were proposed and refined. The most recent congress occurred in 2013 in Rio de Janeiro and the 15 is planned for 2016 in Istanbul.
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抗磷脂综合征(APS)
1983年,医学博士Graham R V Hughes在《英国医学杂志》上发表了一篇两页的文章,题为“血栓、流产、脑病和狼疮抗凝剂”。这通常被认为是第一个将后来被命名为抗磷脂抗体(aPL)的抗体与多种临床症状联系起来的报告,现在被称为抗磷脂抗体综合征(或休斯综合征)。aPL反映了引起/促成病理表现的抗体的异质性集合,以及“假阳性的一般疾病研究实验室(VDRL)”测试和误称的“狼疮抗凝血剂”。自那篇论文发表以来,许多研究小组对休斯博士的观察结果进行了阐述,导致了14次aPL国际大会。在这些会议上,提出并讨论了临床和研究观察结果,提出并完善了诊断标准。最近一次大会于2013年在里约热内卢举行,第15届大会计划于2016年在伊斯坦布尔举行。
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CiteScore
0.30
自引率
0.00%
发文量
7
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