Multiple primary diffuse large B-cell lymphoma masquerading as meningioma

Sivaraman Kumarasamy, K. Garg, Satish Kumar Verma, M. C. Sharma, Ajay Garg, P. S. Chandra, Shashank Sharad Kale
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Abstract

Primary non-Hodgkin’s lymphoma with multiple extra- and intra-calvarial extensions without systemic spread in an immunocompetent patient is extremely rare. They masquerade commonly as meningioma and can present as mass lesions with raised intracranial pressure. We report one such case of primary diffuse large B-cell lymphoma (DLBCL) in a young female involving the scalp, dural involvement in the right frontal region, left parietal, and posterior fossa and mimicking both clinically and radiologically as meningioma. She was managed surgically. Histological examination showed features suggestive of DLBCL (germinal center type). She was planned for adjuvant therapy. However, at 2 months following surgery, she succumbed due to systemic involvement of the disease. DLBCL is seen rarely in neurosurgical practice. They can present as tumors with adjacent extra- and intra-cranial masses. They pose a diagnostic challenge as it can be easily confused with meningioma. Tumor resection is performed to confirm diagnosis and in patients who present with raised intracranial pressure. Chemotherapy is the preferred treatment, and adjuvant therapy should be started early.
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伪装成脑膜瘤的多发性原发性弥漫大 B 细胞淋巴瘤
在免疫功能正常的患者中,原发性非霍奇金淋巴瘤在颅内和颅外多处扩展而无全身扩散的情况极为罕见。我们报告了一例年轻女性原发性弥漫大 B 细胞淋巴瘤(DLBCL)病例,该淋巴瘤累及头皮、右额部硬脑膜、左顶叶和后窝,临床和影像学表现均与脑膜瘤相似。她接受了手术治疗。组织学检查显示其特征提示为 DLBCL(生殖中心型)。计划对她进行辅助治疗。然而,术后2个月,她因全身受累而死亡。DLBCL在神经外科临床上很少见,可表现为肿瘤伴有邻近的颅外和颅内肿块。由于很容易与脑膜瘤混淆,因此给诊断带来了挑战。肿瘤切除术用于确诊和颅内压升高的患者。化疗是首选治疗方法,应尽早开始辅助治疗。
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