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不同细胞类型的多发性神经上皮肿瘤——病例报告

Multiple neuroepithelial tumors of different cell types--case report.

作者信息

Akai T, Takahashi S, Sonobe M, Sugita K

机构信息

Department of Neurosurgery, Mito National Hospital, Japan.

出版信息

Neurol Med Chir (Tokyo). 1995 Dec;35(12):901-4. doi: 10.2176/nmc.35.901.

Abstract

A 31-year-old male developed intramedullary tumors in the medulla oblongata and the upper cervical spinal cord. He was first admitted with tetraparesis. Magnetic resonance (MR) imaging revealed a low intensity mass lesion in the medulla oblongata. The tumor was removed and diagnosed as a pilocytic astrocytoma. Nine years later, he was readmitted with motor weakness and dysesthesia in the right arm. MR imaging revealed a mass lesion in the cervical cord. This tumor was removed and diagnosed histologically as ependymoma. We suggest that the displacement of primitive spongioblasts with subsequent differentiation resulted in an astrocytoma and an ependymoma in adjacent areas.

摘要

一名31岁男性在延髓和颈髓上段出现髓内肿瘤。他最初因四肢轻瘫入院。磁共振成像显示延髓有一个低强度肿块病变。肿瘤被切除,诊断为毛细胞型星形细胞瘤。9年后,他因右臂运动无力和感觉异常再次入院。磁共振成像显示颈髓有一个肿块病变。该肿瘤被切除,组织学诊断为室管膜瘤。我们认为原始成胶质细胞移位并随后分化导致相邻区域出现星形细胞瘤和室管膜瘤。

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