Licandro A, Meneghetti G, Giaretta D
Riv Patol Nerv Ment. 1979 Nov-Dec;100(6):299-308.
Three patients with Jakob-Creutzfeldt disease were studied. The clinical evolution was followed and several EEG controls were made. In all patients characteristic EEG abnormalities were present. Histopathological features in the cortical, subcortical grey matter and in the white matter were examined. Subcortical and cortical grey matter were involved while the white matter appeared intact. The results were compared with previous studies of other Authors and the correlation between the characteristic EEG alterations and the histopathological features was studied in order to explain the appearance of the paroxysmal EEG findings. In agreement with other studies, the Authors emphasized the cortical and subcortical grey matter involvement in the genesis of EEGraphic paroxysmal aspects. The intervention of other factors, possibly of histochemical nature, was postulated.
对三名克雅氏病患者进行了研究。跟踪观察了临床病程,并进行了多次脑电图检查。所有患者均出现了特征性的脑电图异常。对皮质、皮质下灰质和白质的组织病理学特征进行了检查。皮质下和皮质灰质受累,而白质似乎未受影响。将结果与其他作者先前的研究进行了比较,并研究了特征性脑电图改变与组织病理学特征之间的相关性,以解释阵发性脑电图表现的出现。与其他研究一致,作者强调皮质和皮质下灰质受累在脑电图阵发性表现的发生中起作用。推测可能存在其他因素的干预,可能具有组织化学性质。