Sato Kazufumi, Kubota Toshihiko, Ishida Masaki, Handa Yuji
Division of Neurosurgery, Department of Sensory & Locomotor Medicine, Faculty of Medical Science, University of Fukui.
Neurol Med Chir (Tokyo). 2005 Mar;45(3):168-71. doi: 10.2176/nmc.45.168.
A 58-year-old man presented with an extremely rare case of "pure type" spinal tanycytic ependymoma associated with hematomyelia manifesting as sensory disturbance of the bilateral hands and weakness of the right arm. Magnetic resonance imaging demonstrated a tumor in the spinal cord from C-2 to C-4 levels. The soft gelatinous tumor was subtotally resected and the adjacent chronic liquid hematoma was aspirated. The immunohistochemical and ultrastructural findings indicated a diagnosis of tanycytic ependymoma.
一名58岁男性患者,出现了极为罕见的“纯型”脊髓伸长细胞型室管膜瘤,伴有脊髓出血性软化,表现为双手感觉障碍和右臂无力。磁共振成像显示脊髓C2至C4水平有一个肿瘤。将柔软的胶冻状肿瘤次全切除,并抽吸了相邻的慢性液体血肿。免疫组化和超微结构检查结果提示诊断为伸长细胞型室管膜瘤。