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Clinical Characteristics and Management of Cerebral Venous Sinus Thrombosis in Patients With Antiphospholipid Syndrome: A Single-Center Retrospective Study

机译:抗磷脂综合征患者脑静脉血栓形成的临床特征与管理:单中心回顾性研究

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Antiphospholipid syndrome (APS) with cerebral venous sinus thrombosis (CVST) is a relatively rare phenomenon, and this observational study aimed to investigate the clinical characteristics of APS patients complicated with CVST. We retrospectively investigated the clinical characteristics of CVST events in APS and compared differential characteristics and associated factors between APS patients with and without CVST. Twenty-one CVST patients with APS were enrolled including 14 females (9.4%) and 7 males (5.8%). The median age and disease duration at onset of CVST was 33 years (IQR 28-48) old and 1.3 months (IQR 0.7-4), respectively. Among APS patients with CVST, 12 (57.1%) cases presented with neurologic symptoms of CVST as the initial manifestation. Onset of CVST was mainly chronic (52.4%). Headache (90.5%) was the most common neurological symptom. The common locations of CVST were transverse sinus (76.2%) and superior sagittal sinus (57.1%), with more frequently (76.2%) dual or multiple sinuses involved. All patients with CVST were treated with anticoagulant, and 5 (23.8%) patients received endovascular therapy. Sixteen (84.2%) patients had good outcomes and 3 (15.8%) patients died at last follow-up. There were no significant differences ( P 0.05) between two groups in the analysis of related APS indicators. There were no significant differences ( P 0.05) between two groups in the analysis of related APS indicators. Although APS complicated with CVST is rare and predominately chronic developed. The evaluation of CVST should be performed for APS patients with intracranial hypertension syndrome. The routine screening of antiphospholipid antibodies (aPLs) is highly recommended in unexplained CVST patients. Most CVST patients with APS will have a good prognosis after treatment, and endovascular therapy is an alternative treatment.
机译:抗磷脂综合征(APS)具有脑静脉窦血栓形成(CVST)是一种相对罕见的现象,并且该观察性研究旨在调查APS患者复杂的CVST的临床特征。我们回顾性地研究了APS中CVST事件的临床特征,并在没有CVST的情况下比较了APS患者的差异特征和相关因素。已注册二十一只具有AP的CVST患者,包括14名女性(9.4%)和7名男性(5.8%)。 CVST发作的中位年龄和疾病持续时间为33年(IQR 28-48),分别为1.3个月(IQR 0.7-4)。在具有CVST的APS患者中,12例(57.1%)出现CVST的神经系统症状作为初始表现。 CVST的发病主要是慢性(52.4%)。头痛(90.5%)是最常见的神经系统症状。 CVST的常见位置是横向窦(76.2%)和优异的矢状窦(57.1%),更常见(76.2%)双或多个鼻窦。所有CVST患者用抗凝血剂治疗,5例(23.8%)患者接受血管血管治疗。十六(84.2%)患者良好的结果,3名(15.8%)患者在最后一次随访时死亡。在分析相关APS指标的分析中,两组之间没有显着差异(P> 0.05)。在分析相关APS指标的分析中,两组之间没有显着差异(P> 0.05)。尽管APS与CVST复杂的是罕见的,并且主要是慢性发育。应对颅内高血压综合征的APS患者进行CVST的评价。强烈推荐在未解释的CVST患者中常规筛选抗磷脂抗体(APL)。大多数有APS的CVST患者在治疗后会有良好的预后,血管内治疗是一种替代治疗。

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