Eagle Syndrome as a Cause of Cerebral Venous Sinus Thrombosis

被引:11
|
作者
Zhang, Fu-Liang [1 ]
Zhou, Hong-Wei [2 ]
Guo, Zhen-Ni [3 ]
Yang, Yi [1 ,3 ]
机构
[1] Jilin Univ, Hosp 1, Dept Neurol, Stroke Ctr,Neurosci Ctr, Xinmin St 71, Changchun 130021, Jilin, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Radiol, Changchun, Jilin, Peoples R China
[3] Jilin Univ, Hosp 1, Clin Trial & Res Ctr Stroke, Dept Neurol, Changchun, Jilin, Peoples R China
基金
中央高校基本科研业务费专项资金资助; 国家重点研发计划;
关键词
Eagle syndrome; Cerebral venous sinus thrombosis;
D O I
10.1017/cjn.2019.17
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A 15-year-old teenager presented with a 2-month history of headache. Neurological examination was normal except for papilledema. Further lumbar puncture indicated intracranial hypertension (330 mm H2O). Brain magnetic resonance imaging (MRI) was normal but phase contrast-magnetic resonance venography (PC-MRV) (Figure 1(A)) suggested possible left transverse-sigmoid sinus thrombosis; subsequent contrast-enhanced 3D fat-saturated T1 volumetric isotropic turbo spin echo acquisition (VISTA) MRI (Figure 1(B)) confirmed the pathology. Hyper-coagulable panel results (including six steroid sex hormones, antithrombin III, protein C, protein S, lupus anticoagulant, and anticardiolipin antibodies) were all within normal range. In further examination, computed tomography (CT) venography images (Figure 1(C) and (D)) showed that the left jugular vein was compressed by the styloid process, consistent with Eagle syndrome.(1) The patient who refused the recommended surgical treatment, however, chose anticoagulant therapy consisting of low-molecular weight heparin subcutaneous injection in addition to new oral anticoagulant. At 18-month follow-up, the patient reported no symptoms remained.
引用
收藏
页码:344 / 345
页数:2
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