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青年成人新发隐源性难治性多灶性热性惊厥持续状态:6例病例报告

De novo cryptogenic refractory multifocal febrile status epilepticus in the young adult: a review of six cases.

作者信息

Van Lierde I, Van Paesschen W, Dupont P, Maes A, Sciot R

机构信息

Department of Neurology, University Hospital Gasthuisberg, Katholieke Universiteit Leuven, Belgium.

出版信息

Acta Neurol Belg. 2003 Jun;103(2):88-94.

Abstract

BACKGROUND

Status epilepticus (SE) is a common neurological emergency. In around 10 percent, the etiology of SE is not clear, i.e. cryptogenic SE.

AIM

To describe six young adult patients with de novo cryptogenic multifocal febrile SE with poor outcome.

METHODS

Retrospective chart review.

RESULTS

We describe six patients who presented with de novo SE. All were young adults with an unremarkable previous medical history. In all except one, the family history for epilepsy was negative. All had a febrile illness in the week preceding SE. Investigations were unable to reveal the underlying etiology. SE proved refractory to conventional antiepileptic drug treatment (AED) and anesthesia was required to control seizures. Seizures during SE or ensuing epilepsy were multifocal. Brain pathology in four patients was normal in two and showed changes secondary to seizures in two. Outcome was poor in all cases: one patient died during the course of SE, another patient remained with severe mental and physical disability as well as refractory epileptic seizures, the other four developed refractory multifocal epilepsy. One of these patients died a sudden unexpected death in epilepsy (SUDEP) and one drowned during a seizure.

CONCLUSIONS

Six patients were reviewed who presented with de novo cryptogenic multifocal refractory febrile SE. The possible etiologies are discussed. Based on the similarities in these cases, a distinct refractory SE syndrome might be assumed. Further prospective studies will, however, be required to validate this hypothesis as well as to elucidate its etiology and optimize treatment.

摘要

背景

癫痫持续状态(SE)是一种常见的神经科急症。约10%的SE病因不明,即隐源性SE。

目的

描述6例新发隐源性多灶性热性SE且预后不良的年轻成年患者。

方法

回顾性病历审查。

结果

我们描述了6例新发SE患者。所有患者均为年轻成年人,既往病史无异常。除1例患者外,其余患者的癫痫家族史均为阴性。所有患者在SE发作前一周均有发热性疾病。检查未能揭示潜在病因。SE对传统抗癫痫药物治疗(AED)无效,需要麻醉来控制癫痫发作。SE发作期间或随后发生的癫痫发作均为多灶性。4例患者的脑病理检查结果,2例正常,2例显示继发于癫痫发作的改变。所有病例的预后均较差:1例患者在SE病程中死亡,另1例患者仍有严重的精神和身体残疾以及难治性癫痫发作,其余4例发展为难治性多灶性癫痫。其中1例患者死于癫痫猝死(SUDEP),1例在癫痫发作时溺水。

结论

对6例新发隐源性多灶性难治性热性SE患者进行了回顾。讨论了可能的病因。基于这些病例的相似性,可能存在一种独特的难治性SE综合征。然而,需要进一步的前瞻性研究来验证这一假设,并阐明其病因和优化治疗。

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