摘要
胶质肉瘤是一种罕见的由恶性胶质和肉瘤二种成份组成的原发性中枢种经系统肿瘤，本文报告了１０例经手术、病理证实的胶质肉瘤，占我院同期收治颅内肿瘤８３６例的１．２％，就其临床表现、ＣＴ扫描、手术所见和病理特点及预后的关系，结合文献进行讨论。
Abstract Gliolsarcoma is a rare primary central nervoussyStem tumor composed of malignant glial andsarcomatous elemeflts.The authors report 10 casesof gliosarcoma and review the clinical course,CT scan, operative and pathological features,prognosis and the previous literatures. Thepresentatiom of gliosarcoma is similar to that ofother glioblastomas,with the exception of an incidence of syStemic metastasis and involvement ofdure,bone,and soft tissue.The CT scan appearancedemonstrates the biphasic nature of the tumor andinvolvement of extra -axial structures. Operativeintervention to attempt maximal resection should be the treatment of choice.(Original article on page 577)
出处
《广东医学》
CAS
CSCD
1995年第9期577-578,共2页
Guangdong Medical Journal
