Status epilepticus amauroticus revisited: ictal and peri-ictal homonymous hemianopsia.

Susan Shaw, Paul Kim, David Millett
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引用次数: 14

Abstract

Objective: To describe the clinical, electrographic, and radiographic features of status epilepticus amauroticus, or homonymous hemianopsia associated with partial status epilepticus, in 3 patients w:h subsequent resolution of radiographic abnormalities and visual deficits.

Design: Case series.

Setting: Rancho Los Amigos National Rehabilitation Center in Downey, California, and the Los Angeles County + University of Southern California Medical Center.

Patients: One patient with a single remote seizure and 2 patients with symptomatic partial epilepsy all presented with homonymous hemianopsia.

Intervention: Continuous electroencephalographic monitoring, magnetic resonance imaging, and antiepileptic medical therapy for status epilepticus.

Main outcome measures: Neurologic examination, electroencephalography, and magnetic resonance imaging.

Results: The association of homonymous hemianopsia and restricted diffusion on magnetic resonance imaging led to an initial diagnosis of ischemic infarction in 2 cases despite atypical diffusion-weighted imaging patterns. However, continuous electroencephalogram demonstrated focal epileptiform discharges in 2 cases and repetitive focal seizures in another, suggesting a diagnosis of status epilepticus amauroticus. Homonymous hemianopsia resolved in all 3 patients after escalation of the dosage of anticonvulsant therapy. Follow-up magnetic resonance imaging and electroencephalogram demonstrated complete or near-complete resolution of associated abnormalities.

Conclusions: Status epilepticus amauroticus is an uncommon but important cause of homonymous hemianopsia, and it should be considered in any patient with a history of seizures, fluctuating visual symptoms, or atypical patterns of restricted diffusion involving the occipital cortex. Continuous electroencephalographic monitoring is an important diagnostic tool for the diagnosis of status epilepticus amauroticus, which may have a favorable prognosis when treated with aggressive anticonvulsant therapy.

再谈隐匿性癫痫持续状态:发作期和围发作期同名偏盲。
目的:描述3例无影性癫痫持续状态(或伴有部分癫痫持续状态的同型偏盲)患者的临床、电图和影像学特征,并分析其影像学异常和视力缺陷。设计:案例系列。环境:Rancho Los Amigos国家康复中心在唐尼,加利福尼亚,洛杉矶县和南加州大学医学中心。患者:1例单次远端发作,2例有症状性部分性癫痫,均表现为同名偏盲。干预措施:持续脑电图监测,磁共振成像,抗癫痫药物治疗癫痫持续状态。主要观察指标:神经系统检查、脑电图、磁共振成像。结果:2例患者在磁共振成像上出现同型偏盲和弥散受限,尽管弥散加权成像模式不典型,但仍被初步诊断为缺血性梗死。然而,连续脑电图显示2例局灶性癫痫样放电,另1例反复局灶性癫痫发作,提示隐匿性癫痫持续状态的诊断。在抗惊厥药物剂量增加后,所有3例患者的同型偏盲均消失。随访的磁共振成像和脑电图显示相关异常完全或接近完全解决。结论:隐匿性癫痫持续状态是一种罕见但重要的致盲原因,任何有癫痫发作史、波动视觉症状或累及枕皮质的非典型弥散受限的患者都应考虑其病因。连续脑电图监测是诊断无发作性癫痫持续状态的重要工具,在积极抗惊厥治疗的情况下可能有良好的预后。
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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来源期刊
Archives of neurology
Archives of neurology 医学-临床神经学
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