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Giant solitary primary intracranial lymphoma masquerading as meningioma: a case and review of literature

机译:伪装成脑膜瘤的巨大孤立性原发性颅内淋巴瘤:一例并复习文献

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摘要

Non-Hodgkin's lymphomas (NHL) with intracranial origin are very rare and constitutes about 1-2% of primary central nervous system lymphomas (PCNSL). Diffuse large B cell lymphoma (DLBCL) is the most common subtype of NHL and mostly seen in immunocompromised patients. Therefore, the occurrence of giant solitary DLBCL in an immunocompetent patient is puzzling. We present a case of 68-year-old man who was admitted at our facility with a history of “hypomnesia of two (2) months” duration. Magnetic resonance imaging (MRI) revealed a space occupying lesion in the bilateral frontal lobe and corpus callosum measuring about 5.4cm * 4.6cm * 3.8cm with mixed signal intensities and vasogenic edema around the mass. Radiological, this mass was mistaken for meningioma until histopathological studies revealed DLBCL. Giant solitary primary intracranial lymphomas are very rare and can be mistake for meningioma even with very experience radiologist or neurosurgeon since the radiological features of PCNSL can be very unspecific. We achieved to total resection because of the giant and solitary nature of our case. The prognosis of PCNSL is general very poor when the patient is immunocompromised. In immunocompetent patients, who are well managed with surgery and chemotherapy, the overall survival and quality of life can very encouraging.
机译:颅内起源的非霍奇金淋巴瘤(NHL)非常罕见,约占原发性中枢神经系统淋巴瘤(PCNSL)的1-2%。弥漫性大B细胞淋巴瘤(DLBCL)是NHL最常见的亚型,多数见于免疫功能低下的患者。因此,在具有免疫能力的患者中巨大的孤立性DLBCL的发生令人费解。我们介绍了一例68岁的男子,该男子在我们的设施中入院,病史为“两(2)个月的轻度失眠”。磁共振成像(MRI)显示双侧额叶和体占位病变,大小约为5.4cm * 4.6cm * 3.8cm,肿块周围有混合信号强度和血管性水肿。放射学上,该肿块被误认为脑膜瘤,直到组织病理学研究显示DLBCL。巨大的孤立性原发性颅内淋巴瘤非常罕见,即使有经验丰富的放射科医生或神经外科医生也可能将其误认为脑膜瘤,因为PCNSL的放射学特征可能非常不确定。由于病例的巨大和孤独性,我们实现了全切除。当患者免疫功能低下时,PCNSL的预后通常很差。在接受外科手术和化学疗法治疗的免疫能力强的患者中,总体存活率和生活质量可以令人鼓舞。

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