Ependymoma‐like tumor with mesenchymal differentiation harboring C11orf95 ‐ NCOA1 / 2 or ‐ RELA fusion: A hitherto unclassified tumor related to ependymoma
Autor: | Yoshiko Nakano, Junko Hirato, Yukitomo Ishi, Naoki Okura, Koichi Ichimura, Takanori Hirose, Kazuki Nabeshima, Sumihito Nobusawa, Mikiko Aoki, Toshiyuki Enomoto, Mitsutaka Shiota, Takashi Yao, Natsuko Hama, Atsushi Sasaki, Hideaki Yokoo, Shinya Tanaka, Atsushi Natsume, Akihide Kondo, Reika Kawabata-Iwakawa, Ran Tomomasa, Kohei Fukuoka, Tatsuhiro Shibata, Masahiko Nishiyama, Nozomi Suzuki, Yasuhito Arai, Michihiro Kurimoto, Tooru Inoue, Jun Takahashi, Satoshi Nakata, Yoshiaki Yuba, Yoshiki Shiba, Junya Fujimura |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Ependymoma Pathology medicine.medical_specialty Mesenchymal Differentiation General Neuroscience Ependymal Differentiation Mesenchymal stem cell Histology Biology medicine.disease Pathology and Forensic Medicine Staining Fusion gene 03 medical and health sciences 030104 developmental biology 0302 clinical medicine DNA methylation medicine Neurology (clinical) 030217 neurology & neurosurgery |
Zdroj: | Brain Pathology. 31 |
ISSN: | 1750-3639 1015-6305 |
Popis: | Recurrent fusion genes involving C11orf95, C11orf95-RELA, have been identified only in supratentorial ependymomas among primary CNS tumors. Here, we report hitherto histopathologically unclassifiable high-grade tumors, under the tentative label of "ependymoma-like tumors with mesenchymal differentiation (ELTMDs)," harboring C11orf95-NCOA1/2 or -RELA fusion. We examined the clinicopathological and molecular features in five cases of ELTMDs. Except for one adult case (50 years old), all cases were in children ranging from 1 to 2.5 years old. All patients presented with a mass lesion in the cerebral hemisphere. Histologically, all cases demonstrated a similar histology with a mixture of components. The major components were embryonal-appearing components forming well-delineated tumor cell nests composed of small uniform cells with high proliferative activity, and spindle-cell mesenchymal components with a low- to high-grade sarcoma-like appearance. The embryonal-appearing components exhibited minimal ependymal differentiation including a characteristic EMA positivity and tubular structures, but histologically did not fit with ependymoma because they lacked perivascular pseudorosettes, a histological hallmark of ependymoma, formed well-delineated nests, and had diffuse and strong staining for CAM5.2. Molecular analysis identified C11orf95-NCOA1, -NCOA2, and -RELA in two, one, and two cases, respectively. t-distributed stochastic neighbor embedding analysis of DNA methylation data from two cases with C11orf95-NCOA1 or -NCOA2 and a reference set of 380 CNS tumors revealed that these two cases were clustered together and were distinct from all subgroups of ependymomas. In conclusion, although ELTMDs exhibited morphological and genetic associations with supratentorial ependymoma with C11orf95-RELA, they cannot be regarded as ependymoma. Further analyses of more cases are needed to clarify their differences and similarities. |
Databáze: | OpenAIRE |
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