Chokroverty S, Khedekar R, Derby B, Sachdeo R, Yook C, Lepore F, Nicklas W, Duvoisin R C
Neurology. 1984 Nov;34(11):1451-5. doi: 10.1212/wnl.34.11.1451.
We report the neuropathologic findings in the first patient with recognized glutamate dehydrogenase (GDH) deficiency to come to postmortem examination. He had progressive cerebellar ataxia beginning at age 21. He died at age 47 of pulmonary emboli. Postmortem examination revealed pancerebellar, olivary, and mild pontine atrophy, demyelination of the posterior columns, degeneration of anterior horn and dorsal root ganglion cells, and reduction of myelinated fibers in the sural nerve. In addition, there was neuronal storage of lipopigment diffusely throughout the CNS and the autonomic neurons, with cell distention, atrophy, and loss in selected areas.
我们报告了首例经确诊为谷氨酸脱氢酶(GDH)缺乏症并进行尸检的患者的神经病理学发现。他21岁时开始出现进行性小脑共济失调,47岁死于肺栓塞。尸检显示全小脑、橄榄体及轻度脑桥萎缩,后索脱髓鞘,前角及背根神经节细胞变性,腓肠神经有髓纤维减少。此外,整个中枢神经系统和自主神经元中均有脂褐素的神经元内蓄积,部分区域出现细胞肿胀、萎缩及丢失。