Vital A, Bouillot S, Burbaud P, Ferrer X, Vital C
Neuropathology Department, Victor Segalen University, Bordeaux II, France.
Clin Neuropathol. 2002 Mar-Apr;21(2):77-81.
We report the neuropathological data from a familial case of chorea-acanthocytosis with central and peripheral nervous system involvement. At the age of 34, the patient underwent a peripheral nerve biopsy which was analyzed by light- and electron microscopy. These studies showed a selective reduction in the large diameter myelinated fibre population, with several clusters of regeneration. Remyelinating fibers surrounded by flattened Schwann cell processes were also present. The patient died at the age of 44, and post-mortem macroscopic examination of the brain showed marked atrophy of the caudate. Histological examination of paraffin sections showed almost complete depletion of neurons in the caudate, with severe astrocytic gliosis. The putamen and pallidum were slightly less severely depleted of neurons, but with marked astrocytic gliosis. Diffuse mild gliosis was also evidenced, by immunohistochemistry with anti-GFAP, in the thalamus and subcortical white matter.
我们报告了一例伴有中枢和外周神经系统受累的家族性舞蹈病-棘红细胞增多症的神经病理学数据。患者34岁时接受了外周神经活检,并进行了光镜和电镜分析。这些研究显示大直径有髓纤维数量选择性减少,伴有多个再生簇。还存在由扁平施万细胞突起包绕的再髓鞘化纤维。患者44岁时死亡,死后大脑的宏观检查显示尾状核明显萎缩。石蜡切片的组织学检查显示尾状核神经元几乎完全缺失,伴有严重的星形胶质细胞增生。壳核和苍白球神经元缺失程度稍轻,但也有明显的星形胶质细胞增生。通过抗GFAP免疫组化在丘脑和皮质下白质中也证实存在弥漫性轻度胶质增生。