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良性婴儿局灶性癫痫伴睡眠中中线棘波和尖波:一种新的癫痫综合征还是良性局灶性癫痫的变异型?

Benign infantile focal epilepsy with midline spikes and waves during sleep: a new epileptic syndrome or a variant of benign focal epilepsy?

机构信息

Department of Pediatric Neurology, National Pediatric Hospital, Buenos Aires, Argentina.

出版信息

Epileptic Disord. 2010 Sep;12(3):205-11. doi: 10.1684/epd.2010.0320.

Abstract

OBJECTIVE

To analyze the electroclinical features and evolution of seven infants with benign infantile focal epilepsy with midline spikes and waves during sleep (BIMSE).

MATERIAL AND METHODS

Seven patients were examined at our department between February 2003 and February 2009, with onset of seizures between six and 13 months of age (mean, 10.2 months; median, 11 months). Patients with cryptogenic and symptomatic focal epilepsies were excluded. Sex, age, familial history, type of seizures and AED treatment were noted and EEG monitoring, MRI and CT scanning, and developmental and psychomotor evolution were investigated.

RESULTS

Patients included five males and two females. All patients suffered from seizures during wakefulness. Two of the patients (29%) did not have a recurrence. Five (71%) had sporadic seizures (ranging between two and five). One of the seven patients (14%) presented with seizures in clusters. During seizures, staring was observed in six (86%), motion arrest in five (71%), stiffening in five (71%), cyanosis in three (42%), automatisms in one (14%) and lateralizing signs in four (57%). Two patients (29%) had secondary generalisation. The duration of the seizures ranged between 30 seconds and five minutes. No status epilepticus was observed. The interictal EEG recording during sleep showed low-voltage unilateral or bilateral spikes located in the central and vertex regions, followed by slow waves in all patients. Outcome was excellent in all patients.

CONCLUSION

We believe that BIMSE is a new syndrome rather than an early presentation of benign epilepsy of childhood with centrotemporal spikes, Panayiotopoulos syndrome, or a late presentation of benign focal infantile seizures.

摘要

目的

分析 7 例良性婴儿局灶性癫痫伴睡眠中中线棘波和尖波(BIMSE)患儿的临床电特征和演变。

材料与方法

2003 年 2 月至 2009 年 2 月期间,我们科室检查了 7 名患者,发病年龄为 6 至 13 个月(平均 10.2 个月;中位数 11 个月)。排除隐源性和症状性局灶性癫痫患者。记录性别、年龄、家族史、发作类型和 AED 治疗情况,并进行脑电图监测、MRI 和 CT 扫描以及发育和精神运动演变的研究。

结果

患者包括 5 名男性和 2 名女性。所有患者在清醒时均有癫痫发作。2 名患者(29%)未复发。5 名患者(71%)有散发性发作(发作次数为 2 至 5 次)。7 名患者中的 1 名(14%)出现发作群集。在发作期间,6 名患者(86%)出现凝视,5 名患者(71%)出现运动停止,5 名患者(71%)出现僵硬,3 名患者(42%)出现发绀,1 名患者(14%)出现自动症,4 名患者(57%)出现偏侧体征。2 名患者(29%)出现继发性全面性发作。发作持续时间为 30 秒至 5 分钟,无癫痫持续状态。所有患者的睡眠期脑电图均显示中央和顶点区低电压单侧或双侧棘波,随后出现慢波。所有患者的预后均良好。

结论

我们认为 BIMSE 是一种新的综合征,而不是儿童良性癫痫伴中央颞区棘波、Panayiotopoulos 综合征的早期表现,也不是儿童良性局灶性癫痫的晚期表现。

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