Ho K L, Hoschner J A, Wolfe D E
Arch Neurol. 1981 Oct;38(10):662-6. doi: 10.1001/archneur.1981.00510100090018.
Gliomas that arise primarily in the leptomeninges are rare. Of the 15 reported cases of primary leptomeningeal glioma, only two diffusely involved the leptomeninges. We report the third case of primary leptomeningeal gliomatosis, this in a 55-year-old man who died three months after the onset of symptoms. The clinical manifestations, CSF findings, and the gross appearance of the brain resembled meningitis rather than neoplasm. Results of cytologic examinations of the CSF were normal and the diagnosis was made at necropsy. The diffuse form of primary leptomeningeal glioma has a shorter clinical course and poorer prognosis than the solitary form. Primary leptomeningeal gliomas are believed to arise from heterotopic neuroglial tissue in the leptomeninges.
主要起源于软脑膜的胶质瘤很罕见。在已报道的15例原发性软脑膜胶质瘤病例中,只有两例软脑膜呈弥漫性受累。我们报告第三例原发性软脑膜胶质瘤病,患者为一名55岁男性,症状出现三个月后死亡。临床表现、脑脊液检查结果以及大脑的大体外观更像脑膜炎而非肿瘤。脑脊液细胞学检查结果正常,诊断是在尸检时做出的。原发性软脑膜胶质瘤的弥漫型比孤立型临床病程更短,预后更差。原发性软脑膜胶质瘤被认为起源于软脑膜中的异位神经胶质组织。