Sato Kazufumi, Kubota Toshihiko, Ishida Masaki, Yoshida Kazuhiko, Takeuchi Hiroaki, Handa Yuji
Department of Neurosurgery, Fukui Medical University, 23 Shimoaizuki, Yoshida-gun, Matsuoka-cho, 910-1193 Fukui, Japan.
Acta Neuropathol. 2003 Aug;106(2):176-80. doi: 10.1007/s00401-003-0713-2. Epub 2003 May 14.
A chordoid glioma in the third ventricle was studied immunohistochemically and ultrastructurally. In this report, special attention is paid to the histogenesis in relation to the pathological appearance and unique anatomic location of this tumor. Light microscopic and immunohistochemical findings were similar to those reported previously. Ultrastructurally, microvilli were frequently seen, but three types of abnormal cilia were rarely observed. Basement membrane around the tumor cells and microvessels was extensive. Poorly to moderately developed intermediate (adherent) junctions were frequently seen. Resemblance of these ultrastructural features of the tumor to embryonic tanycytes suggests the tanycytic differentiation of chordoid glioma. Neuroradiologically, all of the previously reported cases of chordoid gliomas seem to arise in the anterior part of the third ventricular floor. This region includes the lamina terminalis, infundibular recess and median eminence, which corresponds to a tanycyte-rich area. These findings suggest a tanycytic origin of chordoid glioma.
对一例第三脑室的脊索样胶质瘤进行了免疫组织化学和超微结构研究。在本报告中,特别关注了该肿瘤的组织发生与病理表现及独特解剖位置的关系。光镜和免疫组织化学结果与先前报道的相似。超微结构上,微绒毛常见,但三种异常纤毛罕见。肿瘤细胞和微血管周围的基底膜广泛。常可见发育不良至中等程度的中间(黏附)连接。肿瘤的这些超微结构特征与胚胎性室管膜细胞相似,提示脊索样胶质瘤具有室管膜细胞分化。神经放射学上,先前报道的所有脊索样胶质瘤病例似乎都起源于第三脑室底部前部。该区域包括终板、漏斗隐窝和正中隆起,对应于富含室管膜细胞的区域。这些发现提示脊索样胶质瘤起源于室管膜细胞。