MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1111/bpa.12943

Медицинская библиотека · Brain pathology (Zurich, Switzerland) · 2021

Ependymoma-like tumor with mesenchymal differentiation harboring C11orf95-NCOA1/2 or -RELA fusion: A hitherto unclassified tumor related to ependymoma.

Tomomasa Ran, Arai Yasuhito, Kawabata-Iwakawa Reika, Fukuoka Kohei, Nakano Yoshiko, Hama Natsuko, Nakata Satoshi, Suzuki Nozomi, Ishi Yukitomo, Tanaka Shinya, Takahashi Jun A, Yuba Yoshiaki, Shiota Mitsutaka, Natsume Atsushi, Kurimoto Michihiro, Shiba Yoshiki, Aoki Mikiko, Nabeshima Kazuki, Enomoto Toshiyuki, Inoue Tooru, Fujimura Junya, Kondo Akihide, Yao Takashi, Okura Naoki, Hirose Takanori, Sasaki Atsushi, Nishiyama Masahiko, Ichimura Koichi, Shibata Tatsuhiro, Hirato Junko, Yokoo Hideaki, Nobusawa Sumihito

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Tomomasa Ran, Arai Yasuhito, Kawabata-Iwakawa Reika, Fukuoka Kohei, Nakano Yoshiko, Hama Natsuko, Nakata Satoshi, Suzuki Nozomi, Ishi Yukitomo, Tanaka Shinya, Takahashi Jun A, Yuba Yoshiaki, Shiota Mitsutaka, Natsume Atsushi, Kurimoto Michihiro, Shiba Yoshiki, Aoki Mikiko, Nabeshima Kazuki, Enomoto Toshiyuki, Inoue Tooru, Fujimura Junya, Kondo Akihide, Yao Takashi, Okura Naoki, Hirose Takanori, Sasaki Atsushi, Nishiyama Masahiko, Ichimura Koichi, Shibata Tatsuhiro, Hirato Junko, Yokoo Hideaki, Nobusawa Sumihito. Ependymoma-like tumor with mesenchymal differentiation harboring C11orf95-NCOA1/2 or -RELA fusion: A hitherto unclassified tumor related to ependymoma.. Brain pathology (Zurich, Switzerland). 2021. DOI: 10.1111/bpa.12943.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.