一例左额叶肌样胶质细胞瘤。

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING BJR Case Reports Pub Date : 2024-04-30 eCollection Date: 2024-05-01 DOI:10.1093/bjrcr/uaae014
Jiayi Chu, Sheng Hu, Gangping Wang, Jibo Hu, Wenbo Xiao
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引用次数: 0

摘要

类粘液胶质细胞瘤(MGNT)以前被描述为透明隔的胚胎发育不良性神经上皮肿瘤,在2021年第五版《世界卫生组织中枢神经系统肿瘤分类》中被归类为一种新的肿瘤类型。该分类基于其解剖位置、影像特征和遗传特征。多发性神经胶质瘤在临床上非常罕见,而且容易被误诊。在本报告中,我们介绍了一例左额叶多发性神经胶质瘤病例,该病例经手术病理证实。
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One case of myxoid glioneuronal tumour in the left frontal lobe.

Myxoid glioneuronal tumour (MGNT), previously described as dysembryoplastic neuroepithelial tumour of the septum pellucidum, was classified as a new tumour type in the fifth edition of the WHO Central Nervous System Tumor Classification of 2021. This classification was based on its anatomical location, imaging features, and genetic characteristics. MGNTs are clinically rare and prone to misdiagnosis. In this report, we present a case of MGNT in the left frontal lobe, which was confirmed through surgical pathology.

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BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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发文量
77
审稿时长
11 weeks
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