Seino M, Fujiwara T, Miyakoshi M, Yagi K
Folia Psychiatr Neurol Jpn. 1980;34(3):257-69. doi: 10.1111/j.1440-1819.1980.tb01533.x.
Five patients with the Lennox-Gastaut syndrome who have shown generalized nonconvulsive seizures were presented. The seizure manifestations which occurred spontaneously were documented by simultaneous recording and analyzed in terms of clinical and electroencephalographic correlates. According to the diagnostic criteria of the International Classification, it was possible, on the one hand, to regard them as "atypical complex absences" in which the impairment of consciousness is accompanied by other symptoms, which tend to dominate the clinical picture. They were: hypotonic, hypertonic, myoclonic and akinetic components, respectively. On the other hand, if we give a special weight to the accompanying symptoms, it is entirely possible that they are at the same time diagnosed atonic, axial tonic, bilateral myoclonic and akinetic seizures. The initial impairment of consciousness is common to all the seizure manifestations, and the ictal and interictal EEG expressions are not of diagnostic significance. A question arises as to whether two different nomenclatures were arbitrarily given to a unique ictal manifestation or not as far as the generalized non-convulsive seizures were concerned.
本文报告了5例患有Lennox-Gastaut综合征且表现为全身性非惊厥性发作的患者。通过同步记录自发出现的发作表现,并根据临床和脑电图相关性进行分析。根据国际分类的诊断标准,一方面,有可能将它们视为“非典型复杂失神发作”,其中意识障碍伴有其他症状,这些症状往往主导临床症状。它们分别是:低张力、高张力、肌阵挛和运动不能成分。另一方面,如果特别重视伴随症状,完全有可能同时将它们诊断为失张力性、轴性强直性、双侧肌阵挛性和运动不能性发作。意识的初始障碍是所有发作表现共有的,发作期和发作间期的脑电图表现没有诊断意义。就全身性非惊厥性发作而言,对于一种独特的发作表现是否被任意赋予了两种不同的命名法,这是一个问题。