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先天性髓鞘形成不足性神经病:颅神经和脊神经根中的胶质束。

Congenital hypomyelination neuropathy: glial bundles in cranial and spinal nerve roots.

作者信息

Towfighi J

出版信息

Ann Neurol. 1981 Dec;10(6):570-3. doi: 10.1002/ana.410100614.

Abstract

Autopsy examination of a 3 1/4-year-old child with a severe congenital hypomyelination neuropathy showed the anterior spinal nerve roots and motor cranial nerves to be almost devoid of myelin in their subarachnoid course. The posterior spinal nerve roots and peripheral nerves were less severely affected. Onion bulb formation was minimal and was present only in the sural nerve. There was extensive glial overgrowth in cranial nerves and spinal nerve roots adjacent to the brainstem and spinal cord. The extent and severity of glial overgrowth were similar to that described in Werdnig-Hoffmann disease and morphologically appeared as glial bundles. These glial bundles are most likely secondary to chronic myelin and axonal damage.

摘要

对一名患有严重先天性髓鞘形成不足神经病的3岁3个月大儿童进行尸检,结果显示脊髓前神经根和运动性颅神经在蛛网膜下行程中几乎没有髓鞘。脊髓后神经根和周围神经受影响较轻。洋葱球形成极少,仅在腓肠神经中出现。在脑干和脊髓附近的颅神经和脊髓神经根中有广泛的胶质细胞过度生长。胶质细胞过度生长的范围和严重程度与韦尼克-霍夫曼病中描述的相似,形态上表现为胶质束。这些胶质束很可能继发于慢性髓鞘和轴突损伤。

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