Schlenska G K, Walter G F
Department of Neurology, Niedersächsisches Landeskrankenhaus Hildesheim, Federal Republic of Germany.
J Neurol. 1989 Dec;236(8):456-60. doi: 10.1007/BF00328506.
Frequent serial EEG investigations of three patients with neuropathologically confirmed Creutzfeldt-Jakob disease lasting 13, 24 and 68 weeks revealed typical periodic activity of short duration with stereotyped bilateral sharp waves at the 7th, 8th, and 12th week, respectively, after the onset of symptoms. During the later stages, there were several deviations from this typical pattern. However, periodic activity was preceded between the 3rd and 9th week by intermittent localized or lateralized delta rhythms, which gradually changed into periodic activity. This early temporal evolution of EEG abnormalities may be helpful in the early diagnosis of Creutzfeldt-Jakob disease when accompanied by other investigations to exclude other causes of intermittent delta rhythms.
对三名经神经病理学确诊为克雅氏病的患者进行了为期13周、24周和68周的频繁系列脑电图检查,结果显示,在症状出现后的第7周、第8周和第12周,分别出现了典型的短程周期性活动,并伴有双侧刻板锐波。在后期阶段,出现了一些与这种典型模式的偏差。然而,在第3周和第9周之间,周期性活动之前出现了间歇性局灶性或偏侧性δ节律,这些节律逐渐转变为周期性活动。脑电图异常的这种早期时间演变,在伴有其他检查以排除间歇性δ节律的其他病因时,可能有助于克雅氏病的早期诊断。