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一例以癫痫发作为前驱症状的亚急性硬化性全脑炎:脑电图的演变性变化

A case of subacute sclerosing panencephalitis preceded by epileptic seizures: evolutional EEG changes.

作者信息

Kubota Tetsuo, Okumura Akihisa, Takenaka Junko, Ishiguro Yoshiko, Takahashi Hideaki, Ueda Norishi, Negoro Tamiko, Watanabe Kazuyoshi

机构信息

Department of Pediatrics, Nagoya University School of Medicine, 65 Tsurumai-cho, Showa-Ku, Nagoya, Aichi 466-8550, Japan.

出版信息

Brain Dev. 2003 Jun;25(4):279-82. doi: 10.1016/s0387-7604(02)00231-0.

Abstract

We reported a patient with subacute sclerosing panencephalitis (SSPE) in whom EEG had been serially performed before the onset. She was referred to our hospital due to epileptic seizures at 2 years of age. Focal spikes were seen on EEG at the time of her first seizure (2 years 4 months). At the time of the second unprovoked seizure (9 years 8 months), EEG showed poorly organized background activity associated with focal spikes and a few diffuse spike-and-waves. Then, diffuse paroxysms became predominant, followed by periodic synchronous discharges. In our case, EEG abnormalities were recognized before mental deterioration. Unexpected EEG changes in a patient with epilepsy could be a clue as to the diagnosis of SSPE.

摘要

我们报告了一例亚急性硬化性全脑炎(SSPE)患者,其在发病前已连续进行脑电图(EEG)检查。她因2岁时癫痫发作被转诊至我院。首次癫痫发作(2岁4个月)时,EEG可见局灶性棘波。第二次无诱因癫痫发作(9岁8个月)时,EEG显示背景活动组织紊乱,伴有局灶性棘波和少量弥漫性棘慢波。随后,弥漫性阵发活动占主导,接着出现周期性同步放电。在我们的病例中,在精神衰退之前就已识别出EEG异常。癫痫患者中意外的EEG变化可能是SSPE诊断的线索。

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