Janzer R C, Barontini F
J Neurol. 1985;231(6):319-23. doi: 10.1007/BF00313709.
Clinical and neuropathological data of a 50-year-old woman with an unusual multisystem degeneration are presented. Clinically the illness was characterized by progressive ataxia with ophthalmoplegia and multiple cranial nerve palsies. Neuropathological investigation showed a severe and selective degeneration of the dentato-rubral system, of the posterior columns and of several cranial nerve nuclei. The problems of differential diagnosis and classification are discussed.
本文报告了一名50岁患有罕见多系统变性女性的临床和神经病理学资料。临床上,该疾病的特征为进行性共济失调伴眼肌麻痹和多条颅神经麻痹。神经病理学检查显示齿状核-红核系统、后索及多个颅神经核严重且选择性地变性。文中讨论了鉴别诊断和分类的问题。