Spontaneous intracranial hypotension syndrome presented with sixth cranial nerve palsy: a case report

P. Sousa-Santos, P. Pozzobon, Ana Flavia Andrade Lemos, C. Vieigas, Gilberto Magioni Junior, T. Alvarenga, I. Teixeira, L. C. Lopes
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Abstract

Introduction Spontaneous intracranial hypotension (SIH) is a secondary cause of headache often misdiagnosed and underdiagnosed disorder. The main presentation is orthostatic headache. An uncommon symptom is cranial nerve palsy. We described a case of SIH that presented to our service with sixth cranial nerve palsy. Case Report Female, 39 years old, no relevant medical past or history of trauma, awoke due intense holocranial headache, associated with vomiting and photophobia, worsening in orthostasis. In the general emergency department, she was release with prescription of analgesics and topiramate, without resolution. After a week, the patient reported diplopia and was referred to our service, a tertiary center. In admission, she kept an intense orthostatic headache and in neurologic examination she presented right sixth nerve palsy, no other deficits. Laboratorial tests were normal, including metabolic and infectious marks. Cerebrospinal fluid (CSF) opening pressure was low (50 mmH2O) and analysis showed elevated protein levels (158mg/dl). MRI showed diffuse pachymeningeal enhancement and venous sinus distension, mainly in superior sagittal venous sinus. CT myelogram detected a spinal CSF leak in transition C1-C2. Initially, performed hydration and bed rest, while patient with partial improvement of headache. An epidural blood patch was then performed using 15ml of autologous blood with compatible contrast and lidocaine. There was complete resolution of pain after the procedure and four weeks later complete resolution of right sixth nerve palsy. Discussion According to International Classification of Headaches Disorders, third edition (ICHD-3), the headache attributed to SIH is descripted as a headache has developed in temporal relation to low CSF pressure (<60mm H2O) and/or evidence of CSF leakage on imaging.   (To see the complete abstract, please, check out the PDF).
自发性颅内低血压综合征表现为第六脑神经麻痹:1例报告
自发性颅内低血压(SIH)是头痛的次要原因,常被误诊和漏诊。主要表现为直立性头痛。脑神经麻痹是一种罕见的症状。我们描述了一例SIH,提出了我们的服务与第六脑神经麻痹。病例报告女,39岁,无相关外伤病史,因剧烈颅脑头痛醒来,伴有呕吐和畏光,直立性加重。在普通急诊科,她被释放了镇痛药和托吡酯处方,没有解决。一周后,患者报告复视,并被转介到我们的三级中心。入院时,她一直有强烈的直立性头痛,神经系统检查时,她表现为右第六神经麻痹,无其他缺陷。实验室检查正常,包括代谢和感染痕迹。脑脊液(CSF)开口压力低(50 mmH2O),分析显示蛋白质水平升高(158mg/dl)。MRI示弥漫性厚脑膜增强及静脉窦扩张,以上矢状静脉窦为主。CT髓示示C1-C2过渡期脊髓液渗漏。在患者头痛部分改善时,开始补液和卧床休息。然后用15ml自体血与相容造影剂和利多卡因进行硬膜外补血。术后疼痛完全消失,四周后右侧第六神经麻痹完全消失。根据国际头痛疾病分类,第三版(ICHD-3),归因于SIH的头痛被描述为与脑脊液压力低(<60mm H2O)和/或影像学上脑脊液泄漏证据有关的头痛。(要查看完整的摘要,请查看PDF)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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