Suppr超能文献

裂脑室综合征导致 10 年反复发作的短暂性中央疝病史,表现为癫痫发作:一例脑积水病例报告。

Slit Ventricle Syndrome Leads to 10-Year History of Repetitive Transient Central Herniation Masquerading as Seizures: Hydrocephalus Case Report.

机构信息

Department of Neurosurgery, University of Wisconsin Hospital and Clinics, Madison, Wisconsin, USA.

Department of Neurosurgery, University of Wisconsin Hospital and Clinics, Madison, Wisconsin, USA.

出版信息

World Neurosurg. 2019 Jun;126:134-138. doi: 10.1016/j.wneu.2019.02.106. Epub 2019 Mar 1.

Abstract

BACKGROUND

Slit-ventricle syndrome (SVS) is a recognized complication of ventricular shunt malfunction, resulting in cyclical symptoms without ventricular dilatation. We present a case of SVS with transient, repetitive, and progressive signs of brainstem herniation evidenced by pupillary dilatation, posturing, and unresponsiveness, with diffuse voltage attenuation on electroencephalogram (EEG).

CASE DESCRIPTION

A 32-year-old female presented with a history of hydrocephalus and ventriculoperitoneal shunt placement at 9 months of age. She began experiencing significant headaches in college, later accompanied by stereotypical 5- to 25-minute episodes of unresponsiveness, posturing and pupillary dilatation, and failing anticonvulsant therapy. No neurosurgical evaluation was sought because of small ventricles on brain imaging. Episodes became progressively more frequent over a 10-year period, eventually occurring daily. On presentation, 5 clinical events were captured on EEG over 12 hours of monitoring. With each episode, she became unresponsive and hypertensive, with fixed, dilated pupils and flexor posturing. Between events, she was awake and alert, without confusion or postictal state. She had papilledema and limited extraocular movements, with normal pupils and vital signs. Computed tomography scanning showed small ventricles. A shunt tap revealed no flow. With each episode onset, an EEG revealed an abrupt background rhythm slowing to 2-3 Hz delta range without epileptiform discharges. Between events, EEGs displayed normal waveform activity. Emergent ventriculoperitoneal shunt revision resulted in no further episodes in a 4-year follow-up period.

CONCLUSIONS

SVS can lead to severe intermittent brainstem herniation syndrome in the setting of shunt malfunction. Seizure diagnosis should be reserved for cases with proven functional shunt and EEG confirmation of epileptiform activity.

摘要

背景

裂脑室综合征(SVS)是脑室分流器故障的一种公认并发症,导致无脑室扩张的周期性症状。我们报告了一例 SVS 病例,其表现为短暂、反复、进行性脑干疝的迹象,表现为瞳孔扩大、姿势异常和无反应,脑电图(EEG)显示弥漫性电压衰减。

病例描述

一名 32 岁女性,9 个月大时因脑积水和脑室腹膜分流术而就诊。她在大学时开始出现严重头痛,后来伴有典型的 5 至 25 分钟无反应、姿势异常和瞳孔扩大、抗癫痫治疗失败的发作。由于脑部影像学检查显示脑室较小,因此未进行神经外科评估。在 10 年期间,发作频率逐渐增加,最终每天发作。在就诊时,在 12 小时的监测中,EEG 记录了 5 次临床事件。每次发作时,她都会变得无反应和高血压,瞳孔固定扩大,呈屈肌姿势。在发作之间,她是清醒和警觉的,没有意识模糊或癫痫发作后状态。她有视盘水肿和有限的眼球运动,瞳孔正常,生命体征正常。计算机断层扫描显示脑室较小。分流管穿刺显示无流量。每次发作开始时,EEG 显示背景节律突然减慢至 2-3 Hz 德尔塔范围,没有癫痫样放电。在发作之间,EEG 显示正常的波形活动。紧急脑室腹膜分流器修复后,在 4 年的随访期间没有再发作。

结论

在分流器故障的情况下,SVS 可导致严重间歇性脑干疝综合征。只有在有明确功能分流器且 EEG 证实有癫痫样活动的情况下,才能诊断为癫痫发作。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验