Masuzawa T, Yamamoto H, Sato F
Acta Neuropathol. 1984;62(3):225-9. doi: 10.1007/BF00691856.
The ultrastructure of the wall of the Dandy-Walker cyst has been described rarely. A boy aged 2 years was confirmed clinically, neuroradiologically, and operatively as having a Dandy-Walker cyst in the posterior fossa. The cyst wall obtained during surgery consisted of an outer arachnoid cell layer, intermediate interwoven neurological strands, and an inner layer of cells which lacked the characteristic appearance of ependyma. An unusual finding was a small, buried island of ependymal cells in the intermediate layer of the neuroglial tissue. Ultrastructural study of the cyst wall provides a better understanding of the pathogenesis of the Dandy-Walker syndrome.
丹迪-沃克囊肿壁的超微结构鲜有描述。一名2岁男孩经临床、神经放射学及手术确诊为后颅窝丹迪-沃克囊肿。手术中获取的囊肿壁由外层蛛网膜细胞层、中间交织的神经束以及缺乏室管膜特征性外观的内层细胞组成。一个不寻常的发现是在神经胶质组织中间层有一小片埋入的室管膜细胞岛。对囊肿壁的超微结构研究有助于更好地理解丹迪-沃克综合征的发病机制。