Watanabe Yosuke, Hotta Takuhiro, Yoshioka Hiroyuki, Itou Yoko, Taniyama Kiyomi, Sugiyama Kazuhiko
Department of Neurosurgery and Institute for Clinical Research, National Hospital Organization, Kure medical center, 3-1 Aoyama, Kure City, Hiroshima, Japan.
J Neurooncol. 2008 Jan;86(2):207-10. doi: 10.1007/s11060-007-9459-3. Epub 2007 Jul 13.
We report a 48-year-old woman with primary diffuse leptomeningeal gliomatosis (PDLG) histologically diagnosed as gliosarcoma. She was admitted complaining of headache, numbness of the right arm, double vision, and visual field defects. Computerized tomography (CT) scans showed ventricular dilatation consistent with communicating hydrocephalus. Magnetic resonance imaging (MRI) revealed diffuse meningeal thickening and gadolinium enhancement without a definite intraparenchymal lesion. Whole-spine MRI demonstrated across-the-board dural thickening and gadolinium enhancement. Cytological examination showed atypical anaplastic cells. As no diagnosis could be made she underwent biopsy of the leptomeninges. Histological examination of the specimen returned a diagnosis of gliosarcoma. Despite chemotherapy and radiotherapy she died 11 months after admission. Autopsy findings included gliosarcoma in the leptomeninges and spinal cord without an underlying parenchymal tumor. To our knowledge, this is the first report of primary diffuse leptomeningeal gliosarcomatosis.
我们报告了一名48岁的女性,患有原发性弥漫性软脑膜胶质瘤病(PDLG),组织学诊断为胶质肉瘤。她因头痛、右臂麻木、复视和视野缺损入院。计算机断层扫描(CT)显示脑室扩张,符合交通性脑积水。磁共振成像(MRI)显示弥漫性脑膜增厚和钆增强,无明确的脑实质内病变。全脊柱MRI显示全段硬脑膜增厚和钆增强。细胞学检查显示非典型间变性细胞。由于无法做出诊断,她接受了软脑膜活检。标本的组织学检查结果诊断为胶质肉瘤。尽管进行了化疗和放疗,但她在入院11个月后死亡。尸检结果包括软脑膜和脊髓中的胶质肉瘤,无潜在的脑实质肿瘤。据我们所知,这是原发性弥漫性软脑膜胶质肉瘤病的首例报告。