Drlicek M, Aichholzer M, Wurm G, Bodenteich A, Fischer J
Ludwig Boltzmann Institut für NeuroOnkologie, Landes-Nervenklinik Wagner-Jauregg, Linz.
Pathologe. 2004 Sep;25(5):402-5. doi: 10.1007/s00292-004-0696-3.
A 51 year old caucasian male presented with headache, facial nerve paresis and continuing contraction of the visual field. CT scan revealed a singular intracerebral contrast enhancing lesion in the left frontal lobe. Intraoperatively the tumour was well demarcated. Frozen sections showed a high grade glioma. Paraffin sections revealed, in addition to the gliomatous component, some sharply demarcated nests of meningothelial cells. Immunohistochemistry with glial fibrillary acidic protein and epithelial membrane antigen confirmed a collision tumour consisting of a glioblastoma WHO-grade IV and a meningothelial meningioma WHO-grade I. The coincidence of these two different tumours at the same time and the same location leads us to the speculation, that the collision tumour might have been caused by malignant transformation of a reactive astrogliosis surrounding the meningioma.
一名51岁的白种男性患者出现头痛、面神经麻痹和视野持续缩小。CT扫描显示左额叶有一个单一的脑内强化病灶。手术中肿瘤界限清楚。冰冻切片显示为高级别胶质瘤。石蜡切片显示,除了胶质瘤成分外,还有一些界限清晰的脑膜内皮细胞巢。胶质纤维酸性蛋白和上皮膜抗原免疫组化证实这是一个碰撞瘤,由世界卫生组织IV级胶质母细胞瘤和世界卫生组织I级脑膜内皮型脑膜瘤组成。这两种不同肿瘤同时出现在同一位置,促使我们推测,这个碰撞瘤可能是由脑膜瘤周围反应性星形胶质细胞增生的恶性转化引起的。