Yazıcı Ayten
Division of Rheumatology, Department of Internal Medicine, Kocaeli University School of Medicine, Kocaeli, Turkey.
Eur J Rheumatol. 2020 Oct;7(4):180-183. doi: 10.5152/eurjrheum.2020.20099.
Antiphospholipid syndrome (APS) is characterized by thrombosis and/or pregnancy morbidity with persistently positive antiphospholipid antibodies. However, in APS, there are several non-thrombotic clinical manifestations such as thrombocytopenia, cardiac valve disease, microthrombotic nephropathy, skin ulcer, or cognitive dysfunction. These non-criteria manifestations are relatively common and usually are non-responsive to anticoagulation. Among the non-criteria manifestations, thrombocytopenia, skin ulcers, migraine, and heart valve lesions are the most frequent manifestations described in APS. Limited data are available on the treatment of non-criteria manifestations of APS, and most therapeutic options are based on case reports or retrospective non-randomized studies. Although there is no consensus on the treatment of non-criteria manifestations of APS, anticoagulant therapy and immunomodulatory drugs could be combined in most patients.
抗磷脂综合征(APS)的特征是血栓形成和/或妊娠并发症伴抗磷脂抗体持续阳性。然而,在APS中,存在多种非血栓性临床表现,如血小板减少、心脏瓣膜病、微血管血栓性肾病、皮肤溃疡或认知功能障碍。这些非标准表现相对常见,通常对抗凝治疗无反应。在非标准表现中,血小板减少、皮肤溃疡、偏头痛和心脏瓣膜病变是APS中描述最多的表现。关于APS非标准表现的治疗数据有限,大多数治疗选择基于病例报告或回顾性非随机研究。尽管对于APS非标准表现的治疗尚无共识,但在大多数患者中可联合使用抗凝治疗和免疫调节药物。