Nagaishi Masaya, Yokoo Hideaki, Nobusawa Sumihito, Fujii Yoshiko, Sugiura Yoshiki, Suzuki Ryotaro, Tanaka Yoshihiro, Suzuki Kensuke, Hyodo Akio
Department of Neurosurgery, Dokkyo Medical University Koshigaya Hospital, 2-1-50 Minami-Koshigaya, Koshigaya-shi, Saitama, 343-8555.
Department of Human Pathology, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi-shi, Gunma, 371-8511, Japan.
Neuropathology. 2015 Dec;35(6):561-8. doi: 10.1111/neup.12217. Epub 2015 Jun 14.
Multinodular and vacuolating neuronal tumors (MVNT) have been recently referred to as a distinctive neuronal tumor entity based on histopathological findings. They are characterized by multiple tumor nodules, vacuolar alteration and widespread immunolabeling for human neuronal protein HuC/HuD. Only 13 cases have been reported in the literature to date and little is known about the histopathology of these tumors. Herein, we report a case of MVNT with additional confirmation of immunohistochemical features. A 22-year-old woman presented with a continuous headache. MRI showed a subcortical white matter lesion with multiple satellite nodules in the frontal lobe appearing as T2/fluid-attenuated inversion recovery (FLAIR) hyperintensities. Histological examination of the resected lesion revealed well-defined multiple nodules composed of predominant vacuolating tumor cells. The tumor cells exhibited consistent immunolabeling for doublecortin, as well as HuC/HuD, both representative neuronal biomarkers associated with earlier stages of neuronal development. Immunopositivity for oligodendrocyte transcription factor 2 (Olig2) and S100 was also detected in tumor cells. Additionally, significant overexpression of alpha-internexin was observed in the background neuropil limited to tumor nodules. Neuronal nuclear antigen (NeuN), synaptophysin and neurofilament, markers for mature neurons, were either negative or weakly positive. The expression profile of neuronal biomarkers can be distinguished from that of classic neuronal tumors and is the immunohistochemical hallmark of MVNT. In summary, we identified the characteristic tumoral expression of HuC/HuD and doublecortin and the presence of abundant neuropil localized in MVNT tumor nodules, which exhibited widespread alpha-internexin expression. These results supported the presumption that MVNT is a distinct histopathological entity.
多结节性空泡状神经元肿瘤(MVNT)最近基于组织病理学发现被认为是一种独特的神经元肿瘤实体。它们的特征是多个肿瘤结节、空泡样改变以及广泛的人神经元蛋白HuC/HuD免疫标记。迄今为止,文献中仅报道了13例,对这些肿瘤的组织病理学了解甚少。在此,我们报告一例MVNT,并进一步证实其免疫组化特征。一名22岁女性因持续性头痛就诊。磁共振成像(MRI)显示额叶皮质下白质病变,伴有多个卫星结节,在T2加权/液体衰减反转恢复序列(FLAIR)上呈高信号。对切除病变的组织学检查显示,有界限清楚的多个结节,主要由空泡状肿瘤细胞组成。肿瘤细胞对双皮质素以及HuC/HuD均表现出一致的免疫标记,这两种都是与神经元发育早期阶段相关的代表性神经元生物标志物。在肿瘤细胞中还检测到少突胶质细胞转录因子2(Olig2)和S100的免疫阳性。此外,在仅限于肿瘤结节的背景神经纤维网中观察到α-中间丝蛋白明显过表达。成熟神经元的标志物神经元核抗原(NeuN)、突触素和神经丝蛋白呈阴性或弱阳性。神经元生物标志物的表达谱可与经典神经元肿瘤相区分,是MVNT的免疫组化标志。总之,我们在MVNT肿瘤结节中鉴定出HuC/HuD和双皮质素的特征性肿瘤表达以及大量神经纤维网的存在,且这些结节表现出广泛的α-中间丝蛋白表达。这些结果支持MVNT是一种独特组织病理学实体的推测。