Kubota Tetsuo, Okumura Akihisa, Takenaka Junko, Ishiguro Yoshiko, Takahashi Hideaki, Ueda Norishi, Negoro Tamiko, Watanabe Kazuyoshi
Department of Pediatrics, Nagoya University School of Medicine, 65 Tsurumai-cho, Showa-Ku, Nagoya, Aichi 466-8550, Japan.
Brain Dev. 2003 Jun;25(4):279-82. doi: 10.1016/s0387-7604(02)00231-0.
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.
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。