Bannister C M, Mundy J E
Acta Neurochir (Wien). 1979;46(1-2):159-68. doi: 10.1007/BF01407689.
Two hydrocephalic Hy 3 mice and an infant with hydrocephalus and the Arnold-Chiari malformation were examined with the scanning electron microscope. Both mice had advanced hydrocephalus but had normal appearances in the basal regions of the ventricles. However, as the ventricular walls were ascended first the cilia gradually disappeared, then the microvilli, and finally on the roof of the ventricle the ependymal cells disappeared leaving the subependymal layers exposed. The infant had mild hydrocephalus and normal ependymal appearances. The most likely explanation of these findings is that they are a consequence of raised intracranial pressure, and are not the cause of hydrocephalus.
对两只脑积水的Hy 3小鼠以及一名患有脑积水和阿诺德-奇亚里畸形的婴儿进行了扫描电子显微镜检查。两只小鼠均患有晚期脑积水,但脑室基底区域外观正常。然而,随着沿着脑室壁向上观察,纤毛逐渐消失,接着微绒毛消失,最后在脑室顶部室管膜细胞消失,露出室管膜下层。该婴儿患有轻度脑积水,室管膜外观正常。这些发现最可能的解释是,它们是颅内压升高的结果,而非脑积水的病因。