Radiological approach to multinodular and vacuolating neuronal tumor: Two case report

S. O. Ocak Karatas, M. Beyhan, E. Gökçe
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Abstract

Multinodular and vacuolating neuronal tumors (MVNT) are indolent, low-grade, superficial neuronal tumors of the cerebrum that consist only of neuronal cells in adults. They were first reported in 2013 by Huse et al. and defined by the World Health Organization in 2016. MVNT is characterized by vacuolated tumor nodules with glial and/or neuronal differentiation histopathologically. MVNT is most commonly located in the temporal lobe. Radiologically, it has a subcortical, soap-bubble morphology, sometimes extending to the cortex, and is almost as hyperintense as cerebrospinal fluid on T2-weighted images. Its signal is not suppressed on the FLAIR sequence, and there is no diffusion restriction on diffusion-weighted images. Usually, there is no enhancement after gadolinium injections, but a few reports show weak enhancement in the literature. In the first case, we present a 22-year-old female with MVNT who underwent MRI for a complaint of dizziness which was detected incidentally. MRI showed a clustered multinodular lesion in the left superior frontal gyrus that was hyperintense on T2-weighted/FLAIR series and isointense with gray matter on T1-weighted images. There was no diffusion restriction or contrast enhancement on MRI. In the second case, a 51-year-old female with complaints of numbness and pain in her left arm had an MRI that showed a lesion in the right cerebral hemisphere at the temporoparietal junction. The lesion did not cause edema or mass effect and was distributed in the cortical-subcortical area. The lesion was hyperintense in T2-weighted and FLAIR series and consisted of many millimetric nodular components in close intensity with gray matter in the T1-weighted series. No contrast enhancement was detected. Knowing the characteristic imaging findings of MVNT is important in avoiding aggressive diagnosis and treatment approaches in asymptomatic cases. In conclusion, MVNT is a newly identified tumor that appears hyperintense on the FLAIR sequence and should not be operated on.
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多结节性和空泡性神经元肿瘤的影像学检查:附2例报告
多结节和空泡性神经肿瘤(MVNT)是一种惰性的、低级别的、浅表的大脑神经肿瘤,仅由神经细胞组成。它们于2013年由house等人首次报告,并于2016年由世界卫生组织定义。MVNT以空泡状肿瘤结节为特征,组织学上呈胶质和/或神经元分化。MVNT最常位于颞叶。影像学表现为皮层下皂泡形态,有时延伸至皮层,在t2加权图像上几乎与脑脊液一样高。它的信号在FLAIR序列上不被抑制,对弥散加权图像没有扩散限制。通常情况下,注射钆后没有增强,但在文献中有少数报道显示弱增强。在第一例病例中,我们报告了一名22岁的女性MVNT患者,她因偶然发现的头晕主诉接受了MRI检查。MRI显示左侧额上回呈簇状多结节状病变,t2加权/FLAIR呈高信号,t1加权呈灰质等信号。MRI未见弥散限制或增强。在第二个病例中,一名51岁女性主诉左臂麻木和疼痛,MRI显示右脑半球颞顶交界处有病变。病变无水肿或肿块效应,分布于皮质-皮质下区。病变在t2加权和FLAIR序列中呈高信号,在t1加权序列中由许多毫米结节组成,与灰质密切相关。未检测到对比度增强。了解MVNT的特征性影像学表现对于避免无症状病例的积极诊断和治疗方法非常重要。总之,MVNT是一种新发现的肿瘤,在FLAIR序列上表现为高信号,不应手术治疗。
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