Yamanouchi H, Matsui R, Tomonaga M, Sakurai H, Yoshimura M, Shimada H
Department of Neurology, Tokyo Metropolitan Geriatric Hospital, Japan.
Acta Neuropathol. 1988;76(3):316-20. doi: 10.1007/BF00687782.
A 77-year-old man suffered intermittent hemiconvulsions of unknown etiology on the left side for a period of about 5 weeks. At the autopsy, there was marked neuronal loss, severe proliferation of astrocytes and spongiform changes in the right cerebral cortex. The cerebral white matter showed loosening with astroglial proliferation in areas on the same side. These neuropathological changes were slight or absent in the left cerebral hemisphere. Histopathological changes were similar to those seen in unilateral Creutzfeldt-Jakob disease (CJD). Although unilateral CJD can not be ruled out, these unilateral hemispheric changes might be induced by intermittent hemiconvulsions.
一名77岁男性左侧出现病因不明的间歇性半身惊厥约5周。尸检时,右侧大脑皮质有明显的神经元丢失、星形胶质细胞严重增生和海绵状改变。大脑白质在同侧区域出现疏松并伴有星形胶质细胞增生。左侧大脑半球的这些神经病理变化轻微或无变化。组织病理学变化与单侧克雅氏病(CJD)所见相似。虽然不能排除单侧CJD,但这些单侧半球变化可能是由间歇性半身惊厥引起的。