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抗磷脂综合征(APS)是一种呈特殊经过的自身免疫性血管病。APS是由体内能引起乏色曼假阳性反应并能抑制止血过程的抗磷脂抗体(包括抗心磷脂抗体和其他抗磷脂抗体)形成过多引起;其病理特征是在各个器官的静脉和/或动脉系统内发生血栓形成;抗磷脂抗体形成过多可以是原发性的,呈慢性经过(敬月至数年),也可在非梅毒性的任何感染性疾病的过程中发生,呈急性经过。APS比较罕见,作者遇见1例老年APs患者,现报告如下:
Antiphospholipid syndrome (APS) is a specially passed autoimmune vascular disease. APS is caused by excessive formation of antiphospholipid antibodies (including anticardiolipin antibodies and other antiphospholipid antibodies) which can cause hypochromic false positive reactions in the body and inhibit the process of hemostasis. The pathological features of APS are caused by the formation of veins in the veins and / or Thrombosis occurs in the arterial system; excessive formation of antiphospholipid antibodies can be primary, chronic (King months to years), can also occur in the course of any non-syphilis infectious disease, was acute . APS is relatively rare, the author met one case of elderly APs, are as follows: