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原发性抗磷脂综合征相关的上矢状窦血栓形成——病例报告

Superior sagittal sinus thrombosis associated with primary antiphospholipid syndrome--case report.

作者信息

Nagai S, Horie Y, Akai T, Takeda S, Takaku A

机构信息

Department of Neurosurgery, Saiseikai Toyama Hospital, Japan.

出版信息

Neurol Med Chir (Tokyo). 1998 Jan;38(1):34-9. doi: 10.2176/nmc.38.34.

Abstract

A 36-year-old female with a history of recurrent pregnancy loss experienced sudden onset of disturbance in consciousness, with right hemiparesis and total aphasia. Computed tomography revealed a massive hemorrhage in the left frontal lobe, and angiography showed occlusion of the anterior two-thirds of the superior sagittal sinus. Laboratory investigations detected the presence of lupus anticoagulant, elevation of the anticardiolipin beta 2-glycoprotein I complex antibody level, and a decreased protein S activity level. There were no underlying conditions, such as connective tissue disorders, malignancies, infectious diseases, and drug-induced disorders, so the diagnosis was primary antiphospholipid syndrome. Primary antiphospholipid syndrome should be considered in the evaluation of patients with "idiopathic" or "primary" sinus and cerebral venous thrombosis.

摘要

一名有复发性流产病史的36岁女性突然出现意识障碍,伴有右侧偏瘫和完全性失语。计算机断层扫描显示左额叶大量出血,血管造影显示上矢状窦前三分之二闭塞。实验室检查发现存在狼疮抗凝物,抗心磷脂β2-糖蛋白I复合物抗体水平升高,蛋白S活性水平降低。不存在结缔组织疾病、恶性肿瘤、传染病和药物性疾病等基础疾病,因此诊断为原发性抗磷脂综合征。在评估“特发性”或“原发性”窦和脑静脉血栓形成的患者时,应考虑原发性抗磷脂综合征。

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