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由光敏性引发的典型失神发作。

Typical absence seizures triggered by photosensitivity.

作者信息

Baykan Betül, Matur Zeliha, Gürses Candan, Aykutlu Ebru, Gökyiğit Ayşen

机构信息

Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.

出版信息

Epilepsia. 2005 Jan;46(1):159-63. doi: 10.1111/j.0013-9580.2005.67303.x.

DOI:10.1111/j.0013-9580.2005.67303.x
PMID:15660784
Abstract

PURPOSE

To describe the characteristics of patients with typical absence seizures (TASs), consistently triggered by photosensitivity.

METHODS

Consecutive patients having TAS induced by intermittent photic stimulation were included in the study. All clinical parameters, EEG, and video-EEG data were assessed during the long-term follow-up. Statistical analyses were performed with SPSS 10.0 software.

RESULTS

Nine female and two male patients with a mean age at onset of 14 +/- 5.9 years (range, 7-27 years) and with a mean follow-up of 9 +/- 7.56 years had photosensitive TASs. They constituted 7.64% of absence epilepsies and 0.4% of all patients seen in our tertiary center. The seizures were usually subtle and had a reported frequency of 1 to 9 times daily. Seven patients were clinically photosensitive and reported that some of their TASs were induced by photic stimuli in daily life. All patients also had spontaneous TASs, and four of them had generalized tonic-clonic seizures. EEG results did not show any distinctive features when compared with those of other cases with TASs. Remission could not be achieved in five patients with antiepileptic drug treatments, and we always observed relapses after drug discontinuation or dose reduction in the remaining six cases in remission. Spontaneous remission did not occur even in the five patients older than 30 years.

CONCLUSIONS

TASs triggered by photosensitivity are a rare and heterogeneous clinical condition with a marked female preponderance. It is notable that TASs do not remit in these cases.

摘要

目的

描述由光敏性持续引发的典型失神发作(TASs)患者的特征。

方法

本研究纳入了由间歇性光刺激诱发TASs的连续患者。在长期随访期间评估所有临床参数、脑电图(EEG)和视频脑电图数据。使用SPSS 10.0软件进行统计分析。

结果

9例女性和2例男性患者有光敏性TASs,平均发病年龄为14±5.9岁(范围7 - 27岁),平均随访时间为9±7.56年。他们占失神癫痫患者的7.64%,占我们三级中心所有就诊患者的0.4%。发作通常较轻微,据报告每日发作频率为1至9次。7例患者临床上对光敏感,报告其部分TASs在日常生活中由光刺激诱发。所有患者也有自发性TASs,其中4例有全身强直阵挛发作。与其他TASs病例相比,EEG结果未显示任何独特特征。5例接受抗癫痫药物治疗的患者未实现缓解,在其余6例缓解的病例中,我们总是观察到停药或减药后复发。即使在5例年龄大于30岁的患者中也未出现自发缓解。

结论

由光敏性引发的TASs是一种罕见且异质性的临床病症,女性明显居多。值得注意的是,这些病例中的TASs不会缓解。

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