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惊吓诱发的癫痫发作:19例患者的特征

Startle provoked epileptic seizures:features in 19 patients.

作者信息

Manford M R, Fish D R, Shorvon S D

机构信息

Wessex Neurological Centre, Southampton General Hospital, Hampshire, UK.

出版信息

J Neurol Neurosurg Psychiatry. 1996 Aug;61(2):151-6. doi: 10.1136/jnnp.61.2.151.

Abstract

OBJECTIVES

To define the clinical characteristics of a group of patients with startle provoked epileptic seizures (SPES).

METHODS

Nineteen patients were identified during the course of a larger study of clinical seizure patterns. A witnessed seizure account was obtained in all patients; interictal EEG in 18, video-EEG-telemetry in eight, CT in 18, and high resolution MRI in eight.

RESULTS

The onset of SPES was in childhood or adolescence in 14 of 19 patients. It was preceded by exclusively spontaneous seizures in nine patients and SPES had been replaced by exclusively spontaneous seizures in two patients. Sudden noise was the main triggering stimulus and somatosensory and visual stimuli were also effective in some patients. The clinical seizure pattern involved asymmetric tonic posturing in 16 of 19 patients. Focal neurological signs were present in nine patients, mental retardation in six, and 10 were clinically normal. Ictal scalp EEG showed a clear seizure discharge in only one patient with a tonic seizure pattern; over the lateral frontal electrodes contralateral to the posturing limbs. Brain CT showed a porencephalic cyst in three patients, focal frontal atrophy in one, and generalised atrophy in one. Brain MRI was undertaken in five normal subjects and three neurologically impaired patients, six with normal CT. It showed a porencephalic cyst in one patient. In six patients, there were dysplastic lesions. They affected the lateral premotor cortex in three patients and the perisylvian cortex in three patients, one with bilateral perisylvian abnormality.

CONCLUSIONS

SPES are more frequent than is generally appreciated. They may be transient and occur relatively commonly without fixed deficit, by contrast with previous reports. The imaging abnormalities identified in those without diffuse cerebral damage suggest that SPES are often due to occult congenital lesions and that the lateral premotor and perisylvian cortices are important in this phenomenon.

摘要

目的

明确一组惊吓诱发癫痫发作(SPES)患者的临床特征。

方法

在一项关于临床癫痫发作模式的更大规模研究过程中,识别出19例患者。所有患者均有目击的癫痫发作记录;18例患者进行了发作间期脑电图检查,8例进行了视频脑电图遥测,18例进行了CT检查,8例进行了高分辨率MRI检查。

结果

19例患者中,14例的SPES起病于儿童期或青少年期。9例患者此前仅有自发性发作,2例患者的SPES已完全被自发性发作所取代。突发噪声是主要的触发刺激因素,躯体感觉和视觉刺激在部分患者中也有效。19例患者中有16例的临床癫痫发作模式表现为不对称强直性姿势。9例患者有局灶性神经体征,6例有智力发育迟缓,10例临床检查正常。发作期头皮脑电图仅1例强直性发作模式的患者显示有明确的癫痫放电,位于与姿势性肢体对侧的外侧额部电极处。脑部CT显示3例患者有脑穿通畸形囊肿,1例有局灶性额叶萎缩,1例有广泛性萎缩。对5名正常受试者和3名神经功能受损患者进行了脑部MRI检查,其中6例CT检查正常。1例患者显示有脑穿通畸形囊肿。6例患者有发育异常性病变。3例患者病变累及外侧运动前皮质,3例患者病变累及岛周皮质,1例双侧岛周异常。

结论

SPES比普遍认为的更为常见。与既往报道相反,它们可能是短暂性的,且相对常见,不伴有固定性缺陷。在无弥漫性脑损伤的患者中发现的影像学异常表明,SPES通常由隐匿性先天性病变引起,外侧运动前皮质和岛周皮质在这一现象中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aeb/1073988/fa8ffa8849f0/jnnpsyc00008-0028-a.jpg

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