Rachwan Rayan Jo, Daher Ghassan E, Fares Jawad, Rachoin Rachoin
Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, United States.
Front Cardiovasc Med. 2017 Sep 20;4:59. doi: 10.3389/fcvm.2017.00059. eCollection 2017.
Native aortic valve thrombosis in primary antiphospholipid syndrome (APLS) is a rare entity. We describe a 38-year-old man who presented with neurological symptoms and a cardiac murmur. Transthoracic echocardiography detected a large bicuspid aortic valve thrombus. Laboratory evaluation showed the presence of antiphospholipid antibodies. Anticoagulation was started, and serial echocardiographic studies showed complete resolution of the aortic valve vegetation after 4 months. The patient improved clinically and had no residual symptoms. This report and review of the literature suggests that vegetations in APLS can be treated successfully with conservative treatment, regardless of their size.
原发性抗磷脂综合征(APLS)中的天然主动脉瓣血栓形成是一种罕见的病症。我们描述了一名38岁男性,他出现了神经系统症状和心脏杂音。经胸超声心动图检测到一个大的二叶式主动脉瓣血栓。实验室检查显示存在抗磷脂抗体。开始抗凝治疗,系列超声心动图研究显示4个月后主动脉瓣赘生物完全消退。患者临床症状改善,无残留症状。本报告及文献综述表明,无论APLS中赘生物的大小如何,保守治疗均可成功治愈。