Department of Neurology, Atrium Medisch Centrum Parkstad, PO Box 4446, 6401 CX, Heerlen, The Netherlands.
J Neurol. 2010 Mar;257(3):349-53. doi: 10.1007/s00415-009-5322-0. Epub 2009 Sep 24.
We report a 71-year-old woman who presented with a cerebral cavernous malformation in the right frontal lobe for which she underwent total resection. Three years later, she was admitted with seizures and neuroimaging revealed a partially calcified lesion in the area of the earlier cavernous malformation, consistent with a residual malformation. A few months later she presented with cognitive decline and neuroimaging now revealed a large mass lesion in the same area as the cavernous malformation, irregularly enhancing, spreading through the corpus callosum to the left frontal lobe. Histological examination showed an anaplastic oligo-astrocytoma. These findings suggest that cerebral cavernous malformations, or at least a subgroup, have the potential for oligodendrocytic and astrocytic transformation. Various hypotheses to explain the etiology of these rare cases are discussed.
我们报告了一例 71 岁女性,因右侧额叶脑内海绵状血管畸形就诊并行全切除手术。3 年后,患者因癫痫发作再次入院,神经影像学检查显示早期海绵状血管畸形区域有部分钙化病变,符合残余畸形。几个月后,患者出现认知功能下降,神经影像学检查显示同一海绵状血管畸形区域出现一个大的肿块病变,呈不规则增强,穿过胼胝体延伸至左侧额叶。组织学检查显示间变性少突-星形细胞瘤。这些发现表明,脑内海绵状血管畸形,或至少其中一个亚组,具有向少突胶质细胞和星形胶质细胞转化的潜力。讨论了各种解释这些罕见病例病因的假说。