Nobusawa Sumihito, Hirato Junko, Sugai Tsutomu, Okura Naoki, Yamazaki Tatsuya, Yamada Seiji, Ikota Hayato, Nakazato Yoichi, Yokoo Hideaki
J Neuropathol Exp Neurol. 2016 Feb;75(2):167-74. doi: 10.1093/jnen/nlv017.
Atypical teratoid/rhabdoid tumors (AT/RT) are rare, aggressive, embryonal brain tumors that occur most frequently in very young children; they are characterized by rhabdoid cells and loss of INI1 protein nuclear expression. Here, we report the case of a 24-year-old man with a left frontal lobe tumor that was composed mainly of rhabdoid cells showing loss of INI1 nuclear reactivity and polyphenotypic immunohistochemical expression, with a small INI1-positive component of ependymoma. Array comparative genomic hybridization separately conducted for each histologically distinct component revealed 22 shared identical copy number alterations, including loss of heterozygosity of chromosome 22q containing the INI1 locus. Furthermore, we found the C11orf95-RELA fusion gene, the genetic hallmark of supratentorial ependymomas, not only in the ependymoma component but also in the AT/RT component by fluorescence in situ hybridization analysis, suggesting that the AT/RT cells secondarily progressed from the preexisting ependymoma cells. A second genetic inactivating event in the INI1 gene was not detected in the AT/RT component. There are several reported cases of AT/RT (or INI1-negative rhabdoid tumors) arising in the setting of other primary brain tumors (gangliogliomas, pleomorphic xanthoastrocytomas, and high-grade gliomas), but the present case
非典型畸胎样/横纹肌样肿瘤(AT/RT)是一种罕见的、侵袭性胚胎性脑肿瘤,最常发生于幼儿;其特征为横纹肌样细胞以及INI1蛋白核表达缺失。在此,我们报告一例24岁男性,其左额叶肿瘤主要由横纹肌样细胞构成,显示INI1核反应性缺失及多表型免疫组化表达,伴有一小部分INI1阳性的室管膜瘤成分。对每个组织学上不同的成分分别进行的阵列比较基因组杂交显示有22个相同的拷贝数改变,包括含有INI1基因座的22号染色体杂合性缺失。此外,我们通过荧光原位杂交分析不仅在室管膜瘤成分中,而且在AT/RT成分中发现了幕上室管膜瘤的基因标志C11orf95-RELA融合基因,提示AT/RT细胞继发于先前存在的室管膜瘤细胞。在AT/RT成分中未检测到INI1基因的第二次遗传失活事件。有几例报道的AT/RT(或INI1阴性横纹肌样肿瘤)发生于其他原发性脑肿瘤(神经节胶质瘤、多形性黄色星形细胞瘤和高级别胶质瘤)背景下,但本病例……