Parekh H C, O'Donovan D G, Sharma R R, Keogh A J
Department of Neurosurgery, Royal Preston Hospital, UK.
Br J Neurosurg. 1995 Apr;9(2):171-8. doi: 10.1080/02688699550041511.
A retrospective study of 17 cases of primary cerebral gliosarcoma is presented. These uncommon highly aggressive intracranial neoplasms were seen at the Royal Preston Hospital, between 1973 and 1992. The patients' ages ranged from 21 to 73 years (mean 52), nine were males and eight were females. They presented with signs and symptoms of a rapidly expanding brain tumour. The diagnosis was suspected on radiological findings and confirmed by histological examination. Treatment involved surgical excision in 15 cases and biopsy in two followed by radiotherapy. Chemotherapy was given in three cases. Despite active management, median survival was only 9 months. The clinical, radiological and pathological features of these lesions are highlighted with emphasis on combined histochemistry and immunohistochemistry. The features of gliosarcoma and glioblastoma are compared and contrasted.
本文对17例原发性脑胶质肉瘤进行了回顾性研究。这些罕见的高侵袭性颅内肿瘤于1973年至1992年间在皇家普雷斯顿医院被发现。患者年龄在21岁至73岁之间(平均52岁),男性9例,女性8例。他们表现出脑肿瘤迅速增大的体征和症状。根据放射学检查结果怀疑诊断,并经组织学检查确诊。15例患者接受了手术切除,2例进行了活检,随后进行放疗。3例患者接受了化疗。尽管积极治疗,中位生存期仅为9个月。重点介绍了这些病变的临床、放射学和病理学特征,强调了联合组织化学和免疫组织化学。比较并对比了胶质肉瘤和胶质母细胞瘤的特征。