摘要
目的原发性中枢神经系统淋巴瘤(PCNSL)较少见,但恶性高,现以9例作一临床分析。方法用病理和免疫组织化学检查证实9例PCNSL,分析其诊断、治疗及预后。结果肿瘤位于大脑深部,呈浸润性生长,CT具有一定的特性,边界一般较清楚,呈略高密度,注射造影剂后增强明显。单纯的手术切除肿瘤无助于延长患者的生存期,多数病例预后恶劣。放疗和化疗有一定疗效。结论PCNSL恶性高,发展快,早期诊断及治疗是延长患者生存期的关键。对脑内深部占位性病变应想到PCNSL的可能。
Objective:Primary central nervous system lymphoma (PCNSL) is rather rare but highly malignant.A clinical analysis of 9 cases was reported.Methods:All cases were confirmed by pathological and immunohistochemical studies.Results:The lesions usually involved the deepseated structures,showed slight hyperdensity in plain CT, and could be enhanced homogeneously following contrast infusion.Because surgical removal of PCNSL provided little benefits for the survival time,CTguided needle biopsy followed by chemotherapy and/or radiotherapy might be an alternative therapeutic measure.Conclusions:PCNSL is highly malignant.When a space occupied lesion occurred in deepseated brain tissue,we should beware of PCNSL.
出处
《肿瘤》
CAS
CSCD
北大核心
1998年第1期5-7,共3页
Tumor
关键词
淋巴瘤
免疫组化
CT
脑肿瘤
诊断
Brain neoplasms Lymphoma,intracranial CT Immunohistochemistry