Kaneto T, Inoue K, Shimoda K, Doi M, Kitagawa T, Kumada H, Miyata H, Ohama E
Department of Neurology, National Nishi-Tottori Hospital, Tottori.
Rinsho Shinkeigaku. 2000 Aug;40(8):801-6.
A 42-year-old man without family history of neurologic disease developed muscle weakness, and wasting associated with tremor and choreiform movement. He died at age 75 with 33 years of total duration of illness. Autopsy revealed neuronal loss and gliosis in the anterior horns of the spinal cord, hypoglossal nuclei, caudate nuclei, putamen, globus pallidus, and substantia nigra. Bunina bodies or Lewy bodies were not seen. Several similar cases with motor neuron disease, dementia and parkinsonism have been reported in the literature. However, this pattern of chronic spinal neostriato-pallido-nigral degeneration has not been reported.
一名无神经系统疾病家族史的42岁男性出现肌肉无力、萎缩,并伴有震颤和舞蹈样动作。他于75岁去世,病程总计33年。尸检发现脊髓前角、舌下神经核、尾状核、壳核、苍白球和黑质存在神经元丢失和胶质细胞增生。未发现布尼纳小体或路易小体。文献中已报道了几例伴有运动神经元病、痴呆和帕金森症的类似病例。然而,这种慢性脊髓新纹状体-苍白球-黑质变性的模式尚未见报道。