抗磷脂综合征与非影像学轴性脊柱性关节炎相关。

Case Reports in Rheumatology Pub Date : 2021-12-01 eCollection Date: 2021-01-01 DOI:10.1155/2021/4359488
Jozélio Freire De Carvalho, Antoniella Fernanda Mendanha Sousa
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引用次数: 0

摘要

在这里,我们描述了一个患者的抗磷脂综合征(APS)与非影像学轴性脊柱炎(NRAS)相关。一名既往有葡萄膜炎病史的31岁女性于2014年3月发生肺血栓栓塞,并接受利伐沙班治疗(20mg /天)。五个月后,她开始抱怨腰痛。骶髂磁共振造影结果正常。实验室检查显示HLA-B27阳性,红斑狼疮抗凝血剂和IgM抗心磷脂存在。对APS和NRAS进行诊断。患者分别给予利伐沙班治疗APS和柳氮磺胺吡啶(2g /天)。由于她的血液中存在狼疮抗凝抗体,她没有接受非甾体抗炎药。6个月后,患者无症状,无腰痛;她的红细胞沉降率、c反应蛋白和维生素D水平也恢复正常,腰痛得到很好的控制,没有新的葡萄膜炎发作。APS也很稳定。据我们所知,这是第一例与APS相关的NRAS病例。
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Antiphospholipid Syndrome Associated with Nonradiographic Axial Spondyloarthritis.

Herein, we describe a patient with antiphospholipid syndrome (APS) associated with nonradiographic axial spondyloarthritis (NRAS). A 31-year-old woman with a past medical history of uveitis experienced a pulmonary thromboembolism in March 2014 and was treated with rivaroxaban (20 mg/day). Five months later, she started complaining of low back pain. The results on contrast-enhanced sacroiliac magnetic resonance imaging were normal. Laboratory tests revealed positive HLA-B27 and the presence of lupus anticoagulant and IgM anticardiolipin. The diagnoses of APS and NRAS were made. The patient was treated with rivaroxaban for APS and sulfasalazine (2 g/day), respectively. As she showed the presence of lupus anticoagulant antibodies in blood, she did not receive nonsteroidal anti-inflammatory drugs. After 6 months, the patient was asymptomatic, without lumbar pain; she also showed normalization of the erythrocyte sedimentation rate and the C-reactive protein and vitamin D levels, good control of lumbar pain, and no new uveitis episodes. The APS was also stable. To the best of our knowledge, this is the first reported case of NRAS associated with APS.

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发文量
35
审稿时长
12 weeks
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