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首页> 外文期刊>Journal of Surgical Case Reports >Primary dural lymphoma mimicking meningioma: a clinical and surgical case report
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Primary dural lymphoma mimicking meningioma: a clinical and surgical case report

机译:模仿脑膜瘤的原发性硬脑膜淋巴瘤:临床和外科病例报告

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Introduction: Primary central nervous system lymphoma and its subtype, primary dural lymphoma, are types of non-Hodgkin's lymphoma that only occur in the central nervous system without any dissemination. They are extremely rare cases of extra nodal lymphomas accounting for 1--5% of intracranial tumors. Case report: We present a patient diagnosed with primary dural lymphoma in right frontal brain region who underwent surgical resection. Histopathological analysis revealed diffuse B-type large cell non-Hodgkin lymphoma. Patient underwent four cycles of R-CHOP and intrathecal methotrexate protocol. Six months postoperative, no signs of newly onset infiltration were present. Discussion: Primary dural lymphoma most likely presents with unusual radiological signs, which can easily be mistaken for meningioma, the main differential diagnosis. A thorough immunological, histopathological and clinical patients profile should be conducted in order to establish the certainty of diagnosis. Although there are few treatment options: surgery, radiotherapy or chemotherapy, there is no established treatment protocol.
机译:简介:原发性中枢神经系统淋巴瘤及其亚型,即硬脑膜淋巴瘤,是非霍奇金淋巴瘤的类型,仅发生于中枢神经系统而没有任何传播。它们是极少见的淋巴结外淋巴瘤,占颅内肿瘤的1-5%。病例报告:我们介绍了一名被诊断为右额脑区域原发性硬脑膜淋巴瘤的患者,该患者接受了手术切除。组织病理学分析显示弥漫性B型大细胞非霍奇金淋巴瘤。患者经历了四个周期的R-CHOP和鞘内注射甲氨蝶呤方案。术后六个月,没有新出现浸润的迹象。讨论:原发性硬脑膜淋巴瘤很可能表现出异常的放射学体征,很容易被误认为脑膜瘤,这是主要的鉴别诊断。为了确定诊断的准确性,应进行全面的免疫学,组织病理学和临床患者资料。尽管几乎没有治疗选择:手术,放疗或化学疗法,但尚无确定的治疗方案。

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