脑淋巴瘤:诊断困境

IF 1.8 Q4 NEUROSCIENCES Annals of Neurosciences Pub Date : 2023-10-19 DOI:10.1177/09727531231203461
Sibgha Khan, Fatima Mubarak, Khurram Minhas, Dureshahwar Kanwar, Robert Chun Chen
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引用次数: 0

摘要

背景:脑淋巴瘤(LC)是原发性中枢神经系统淋巴瘤(PCNSL)的一种罕见的表现,文献中报道的病例很少,表现为弥漫性浸润过程,而不是孤立的肿块。它是一种非霍奇金淋巴瘤,通常起源于b细胞型。我们打算报告这一独特的LC病例,这是一个诊断挑战。方法一名53岁的男性患者在24小时内出现两次癫痫发作,随后出现10-15分钟的术后意识不清。他接受了多次MRI扫描,并对报告感染的病变进行了活检,但他没有从治疗中获益。结果复查影像学,怀疑为LC,要求复查组织病理学,证实为原发性中枢神经系统淋巴瘤。结论LC是一种罕见但确定的PCNSL表现,它与多种其他疾病相似。了解成像模式是重要的,使诊断和区分它从其他模拟条件。
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Lymphomatosis Cerebri: A diagnostic dilemma
Background Lymphomatosis cerebri (LC) is a rare manifestation of primary central nervous system lymphoma (PCNSL) with only a few cases reported in the literature, appearing as diffuse infiltrating process rather than a solitary mass. It is a non-Hodgkin’s type of lymphoma and is usually of the B-cell type origin. Purpose We intend to report this unique case of LC which came across as a diagnostic challenge. Methods A 53-year-old gentleman presented with complaints of two episodes of seizures 24 h apart followed by postictal confusion for 10–15 min. He underwent multiple MRI scans and underwent a biopsy of the lesion which reported infection, but he did not benefit from the treatment. Result The imaging was reviewed, suspicion of LC was raised and a review of histopathology was requested which later confirmed primary CNS lymphoma. Conclusion LC is a rare but established manifestation of PCNSL which mimics multiple other conditions. Understanding of the imaging pattern is important in making the diagnosis and differentiating it from other mimic conditions.
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来源期刊
Annals of Neurosciences
Annals of Neurosciences NEUROSCIENCES-
CiteScore
2.40
自引率
0.00%
发文量
39
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