Rodda R A, Franklin C I
Aust N Z J Surg. 1984 Aug;54(4):387-90.
A 12 year old girl with episodes of left hemiparesis for 9 months was found to have a large, partly calcified brain tumour which at craniotomy presented on the parasagittal and medial surfaces of the right frontal lobe. No dural or falx attachment could be found and naked eye removal of the tumour was achieved. At a second craniotomy 10 weeks later there was recurrent tumour attached to the falx and involving the sagittal sinus. She died 5 months later. Pathologically, almost all this malignant intracranial neoplasm comprised differentiated cartilaginous tumour. Although only a very small amount of undifferentiated mesenchymal tissue was found in the surgical material available for histological study, it is suggested the tumour can be regarded as a predominantly mature mesenchymal chondrosarcoma of the meninges.
一名12岁女孩,有9个月的左侧偏瘫发作史,被发现患有一个大的、部分钙化的脑肿瘤,在开颅手术中发现该肿瘤位于右额叶矢状旁和内侧表面。未发现硬脑膜或大脑镰附着,肿瘤可通过肉眼切除。10周后进行了第二次开颅手术,发现有复发肿瘤附着于大脑镰并累及矢状窦。她在5个月后死亡。病理检查显示,几乎所有这种恶性颅内肿瘤均由分化的软骨肿瘤组成。尽管在可供组织学研究的手术材料中仅发现了极少量未分化的间叶组织,但提示该肿瘤可被视为主要为成熟的脑膜间叶性软骨肉瘤。