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与颅内低压相关的可逆性脑血管收缩综合征和后部可逆性脑病综合征。

Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome associated with intracranial hypotension.

作者信息

Feil Katharina, Forbrig Robert, Thaler Franziska S, Conrad Julian, Heck Suzette, Dorn Franziska, Pfister Hans-Walter, Straube Andreas

机构信息

Department of Neurology, University Hospital, Campus Grosshadern, Marchioninistrasse 15, 81377, Munich, Germany.

German Center for Vertigo and Balance Disorders, University Hospital, Campus Grosshadern, Marchioninistrasse 15, 81377, Munich, Germany.

出版信息

Neurocrit Care. 2017 Feb;26(1):103-108. doi: 10.1007/s12028-016-0320-4.

Abstract

BACKGROUND

Reversible cerebral vasoconstriction syndrome (RCVS) and posterior reversible encephalopathy syndrome (PRES) are both rare disorders. The pathophysiology of both diseases is not yet fully understood.

METHODS

We report the unique case of a 19-year-old comatose woman who was brought to the ER after a series of generalized tonic-clonic seizures 6 days post peridural anesthesia for cesarean section. Vital signs and initial laboratory testing including urine analysis and drug screening were unremarkable. Initial cranial CT scan showed an acute small subdural hematoma (17 mm length × 6 mm width × 30 mm height), cerebral edema with slit ventricles, and slight cerebellar tonsillar herniation as signs of intracranial hypotension. CT angiography depicted narrowing of the proximal intracranial vessels consistent with RCVS. MR imaging was also suggestive of both intracranial hypotension and RCVS and showed, in addition, vasogenic edema consistent with PRES. An extensive CSF leakage involving T1 to L2/L3 was confirmed by spinal MRI.

RESULTS

The patient underwent conservative therapy for intracranial hypotension (e.g., head-down position) as well as epidural blood patch, which led to regression of the clinical symptoms within a few days. Follow-up MRI showed complete resolution of all radiological changes.

CONCLUSIONS

In summary, our patient developed clinical and neuroradiological signs of intracranial hypotension and a combination of PRES and RCVS associated with a CSF leakage caused by peridural anesthesia; by treating the intracranial hypotension, the other syndromes resolved. From a clinical point of view, it is important to look for CSF leakage as a treatable possible cause of PRES and/or RCVS triggered by intracranial hypotension as in our patient postpartum. Moreover, it is vital to obtain a good history as, in cases of suspected CSF leakage with classic postural headache, a recent spinal/cranial procedure is typically present.

摘要

背景

可逆性脑血管收缩综合征(RCVS)和后部可逆性脑病综合征(PRES)均为罕见疾病。两种疾病的病理生理学尚未完全明确。

方法

我们报告了一例独特病例,一名19岁昏迷女性,在剖宫产硬膜外麻醉6天后出现一系列全身强直阵挛性发作,随后被送往急诊室。生命体征及包括尿液分析和药物筛查在内的初始实验室检查均无异常。初始头颅CT扫描显示急性小硬膜下血肿(长17mm×宽6mm×高30mm)、伴有裂隙脑室的脑水肿以及轻微小脑扁桃体疝,提示颅内低压。CT血管造影显示颅内近端血管狭窄,符合RCVS表现。磁共振成像也提示颅内低压和RCVS,此外还显示与PRES一致的血管源性水肿。脊柱MRI证实存在广泛的脑脊液漏,累及T1至L2/L3。

结果

患者接受了颅内低压的保守治疗(如头低位)以及硬膜外血贴治疗,数天内临床症状消退。随访MRI显示所有影像学改变完全消失。

结论

总之,我们的患者出现了颅内低压的临床和神经影像学表现,以及与硬膜外麻醉导致的脑脊液漏相关的PRES和RCVS组合;通过治疗颅内低压,其他综合征得以缓解。从临床角度来看,如我们产后患者这样,寻找脑脊液漏作为由颅内低压引发的PRES和/或RCVS的可治疗潜在病因很重要。此外,获取详细病史至关重要,因为在疑似脑脊液漏伴典型体位性头痛的病例中,通常近期有脊柱/颅脑手术史。

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