Okamoto K, Hirai S, Shoji M, Harigaya Y, Fukuda T
Department of Neurology, Gunma University School of Medicine, Japan.
Acta Neuropathol. 1991;81(3):349-53. doi: 10.1007/BF00305880.
We report the autopsy findings of an 81-year-old patient with short-course sporadic amyotrophic lateral sclerosis lasting approximately 5 months. Pathological findings were probably very early. Light microscopy showed abundant eosinophilic Bunina type inclusions widely distributed not only in the motor neurons of the spinal cord and brain stem but also in neurons of the Onuf's and Clarke's nuclei. Fine structural study revealed that the inclusions seen in the Clarke's nuclei were identical to Bunina bodies observed in anterior horn cells. A direct connection between axonal swelling and perikaryon was often seen in the facial and hypoglossal nuclei and in the spinal cord. Ubiquitin-positive Lewy body-like inclusions and central chromatolysis-like changes were also found in the anterior horn cells.
我们报告了一名81岁患有短病程散发性肌萎缩侧索硬化症患者的尸检结果,病程约5个月。病理结果可能处于非常早期阶段。光学显微镜检查显示,大量嗜酸性的布宁纳型包涵体广泛分布,不仅存在于脊髓和脑干的运动神经元中,还存在于奥努夫核和克拉克核的神经元中。精细结构研究表明,在克拉克核中看到的包涵体与在前角细胞中观察到的布宁纳小体相同。在面神经核、舌下神经核和脊髓中经常可见轴突肿胀与核周体之间的直接联系。在前角细胞中还发现了泛素阳性的路易小体样包涵体和中央性染色质溶解样改变。