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中枢神经系统原发性淋巴瘤:曼尼托巴省的经验及文献综述

Primary lymphoma of the central nervous system: Manitoba experience and literature review.

作者信息

Hobson D E, Anderson B A, Carr I, West M

出版信息

Can J Neurol Sci. 1986 Feb;13(1):55-61. doi: 10.1017/s0317167100035800.

Abstract

We describe eight cases of primary cerebral lymphoma seen in Manitoba from 1980 to 1985. The clinical presentation is similar to other primary brain tumors. The diagnosis should be considered when single or multiple, often deep lesions, show dense enhancement on computerized tomographic (CT) scan, but are avascular at angiography. These tumors are histologically indistinguishable from non-Hodgkins lymphomas arising outside the CNS. The prognosis is poor. However, radiotherapy with or without surgery may offer significant palliation. Although there is no consensus on the value of chemotherapy, corticosteroids alone or multiagent chemotherapy have shown promise in a few cases. For these reasons, histologic diagnosis should be sought in all cases and surgery, radiotherapy, and chemotherapy should be considered, as prolonged survival is possible.

摘要

我们描述了1980年至1985年在马尼托巴省发现的8例原发性脑淋巴瘤病例。其临床表现与其他原发性脑肿瘤相似。当单发或多发、通常为深部病变在计算机断层扫描(CT)上显示明显强化,但血管造影显示无血管时,应考虑作出诊断。这些肿瘤在组织学上与中枢神经系统外发生的非霍奇金淋巴瘤无法区分。预后较差。然而,放疗加或不加手术可能会带来显著的缓解。尽管对于化疗的价值尚无共识,但单独使用皮质类固醇或多药化疗在少数病例中已显示出前景。基于这些原因,所有病例均应寻求组织学诊断,并应考虑手术、放疗和化疗,因为延长生存期是有可能的。

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