Toubi E, Shoenfeld Y
Division of Allergy and Clinical Immunology, Bnai Zion Medical Center, Haifa, Israel.
Clin Rev Allergy Immunol. 2007 Apr;32(2):138-44. doi: 10.1007/s12016-007-0004-0.
Many consensus meetings were organized in an attempt to improve the present criteria for antiphospholipid syndrome (APS) classification. In this regard, a high prevalence of antiphospholipid antibodies in systemic lupus erythematosus patients was reported in association with the presence of livedo reticularis (LR). In these studies, the association between LR, migraine, and the development of thrombosis (strokes, valvular dysfunctions) was evident. During the last decade, it was strongly suggested that many clinical symptoms (LR, valvular dysfunctions) or laboratory features (thrombocytopenia) should be considered as "minor criteria" for APS. The inclusion of these clinical symptoms in the criteria for APS classification could become of additive value especially when they exist together in one patient. This review summarizes the data that question or support this idea.
为了改进目前抗磷脂综合征(APS)的分类标准,组织了多次共识会议。在这方面,有报告称系统性红斑狼疮患者中抗磷脂抗体的高患病率与网状青斑(LR)的存在有关。在这些研究中,LR、偏头痛与血栓形成(中风、瓣膜功能障碍)之间的关联很明显。在过去十年中,强烈建议将许多临床症状(LR、瓣膜功能障碍)或实验室特征(血小板减少症)视为APS的“次要标准”。将这些临床症状纳入APS分类标准可能会增加价值,尤其是当它们同时出现在一名患者身上时。这篇综述总结了质疑或支持这一观点的数据。