Grunnet M L, Donaldson J O
Arch Neurol. 1985 Nov;42(11):1114-6. doi: 10.1001/archneur.1985.04060100100031.
A case of juvenile multisystem degeneration with motor neuron involvement, possibly of familial type, showing many unusual clinical and pathologic features is reported. Eosinophilic intracytoplasmic inclusions were present in some remaining anterior horn cells and motor nerve nuclei of the brain stem as well as in a few neurons of the reticular activating system, the dorsal vagus nuclei, and the intermediolateral cell column. Smaller eosinophilic inclusions were seen in large neurons of the caudate nucleus and putamen, substantia nigra, and subthalamic nucleus.
报告了一例可能为家族性的伴有运动神经元受累的青少年多系统变性病例,该病例呈现出许多不寻常的临床和病理特征。嗜酸性胞质内包涵体存在于一些残留的前角细胞、脑干运动神经核以及网状激活系统、迷走神经背核和中间外侧细胞柱的少数神经元中。在尾状核、壳核、黑质和丘脑底核的大神经元中可见较小的嗜酸性包涵体。