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室管膜外神经细胞瘤的临床病理和遗传学特征。

Clinicopathological and genetic characteristics of extraventricular neurocytomas.

机构信息

Department of Pathology Neurosurgery Radiology, Seoul National University Hospital, College of Medicine, Korea.

出版信息

Neuropathology. 2013 Apr;33(2):111-21. doi: 10.1111/j.1440-1789.2012.01330.x. Epub 2012 Jun 4.

Abstract

Extraventricular neurocytoma (EVN) shares histological features with central neurocytoma, but has a wide morphological spectrum. Little is known regarding its clinicopathologic nature, biological behavior and genetic abnormalities. The aim of this study is to examine the diagnostic criteria, genetic abnormalities and biological behavior of EVN. Clinicopathological and molecular genetic studies were performed in seven EVNs. Among them, three cases showed atypical histology. Immunohistochemically, synaptophysin was robustly positive, but neuronal muclear antigen was positive in only half the cases (4/7cases). Isocitrate dehydrogenase enzyme isoform 1 (IDH1) (H09 immunostaining), α-internexin and p53 were negative in all cases. One case was positive for galectin-3. None of the cases showed IDH1 R132 and IDH2 R172 mutation by direct sequencing. One case showed high polysomy of the epidermal growth factor receptor (EGFR) gene; however, O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation and 1p/19q co-deletion were not detected. Array-based comparative genomic hybridization (CGH) study was performed in two cases, revealing different profiles, with loss and gain of multiple chromosomal loci. Two children (18%) had tumor recurrence after initial surgery, and one of them showed worse histology at recurrence and EGFR high polysomy. One patient died from the disease at 18.5 months after surgery. From our study, we concluded that EVNs were characterized by the absence of p53 overexpression, α-internexin positivity, MGMT promotor methylation and IDH1/IDH2 mutation. Oligodendrocyte transcription factor 2 expression was seen in a scattered positive pattern but quite large numbers of tumor cells were negative. EVN is a WHO grade II tumor but some cases (2/7 cases in our series) can show late recurrence but mortality is low (1/7 cases in our series). CGH study suggested genetic heterogeneity of EVNs and unknown subclassification, which requires verification in more cases.

摘要

室管膜下神经细胞瘤(EVN)具有与中枢神经细胞瘤相似的组织学特征,但具有广泛的形态学谱。关于其临床病理性质、生物学行为和遗传异常知之甚少。本研究旨在探讨 EVN 的诊断标准、遗传异常和生物学行为。对 7 例 EVN 进行了临床病理和分子遗传学研究。其中,3 例表现为非典型组织学。免疫组化显示突触素强阳性,但仅半数病例(4/7 例)神经元核抗原阳性。异柠檬酸脱氢酶酶同工酶 1(IDH1)(H09 免疫染色)、α-中间丝蛋白和 p53 在所有病例中均为阴性。1 例为半乳糖凝集素-3 阳性。所有病例均未通过直接测序显示 IDH1 R132 和 IDH2 R172 突变。1 例显示表皮生长因子受体(EGFR)基因高度多倍体;然而,未检测到 O6-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)启动子甲基化和 1p/19q 共缺失。对 2 例病例进行了基于阵列的比较基因组杂交(CGH)研究,显示出不同的图谱,存在多个染色体位点的缺失和获得。2 例患儿(18%)在初次手术后出现肿瘤复发,其中 1 例在复发时表现出更差的组织学和 EGFR 高度多倍体。1 例患者在手术后 18.5 个月因疾病死亡。根据我们的研究,我们得出结论,EVN 的特征是缺乏 p53 过表达、α-中间丝蛋白阳性、MGMT 启动子甲基化和 IDH1/IDH2 突变。少突胶质细胞转录因子 2 呈散在阳性模式表达,但相当多的肿瘤细胞呈阴性。EVN 是一种 WHO 分级 II 肿瘤,但有些病例(我们系列中的 2/7 例)可能会出现晚期复发,但死亡率较低(我们系列中的 1/7 例)。CGH 研究表明 EVN 的遗传异质性和未知的亚分类,这需要在更多病例中验证。

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