| Literature DB >> 33221956 |
Sho Tamai1, Yoshiko Nakano2, Masashi Kinoshita3, Hemragul Sabit1, Sumihito Nobusawa4, Yasuhito Arai5, Natsuko Hama5, Yasushi Totoki5, Tatsuhiro Shibata5, Koichi Ichimura2, Mitsutoshi Nakada1.
Abstract
C11orf95-RELA fusion or, less frequently, YAP1 fusion is recurrently detected in most cases of supratentorial ependymoma. Other fusions have rarely been reported in some cases of supratentorial ependymoma, and little is known about their pathological or clinical features. Here, we present a case of supratentorial ependymoma with unusual pathological findings and C11orf95-MAML2 fusion. A 23-year-old man was admitted to our hospital because of headache and vomiting. Magnetic resonance imaging revealed a cystic lesion in the right frontal lobe, and gross total resection of the tumor was performed. Pathologically, the tumor was mainly composed of typical ependymal lesions with perivascular pseudorosettes and contained some atypical lesions, with granular and ganglion cell features. The tumor was diagnosed as anaplastic ependymoma, which was classified as grade III on the World Health Organization scale, and found to be RELA fusion-positive in the DNA methylation analysis. However, the tumor was negative for C11orf95-RELA fusion, and RNA sequencing detected C11orf95-MAML2 fusion. The patient has not received adjuvant therapy and has remained alive without any evidence of disease for 30 months, suggesting that the prognosis might be better than that of typical C11orf95-RELA fusion-positive ependymoma.Entities:
Keywords: C11orf95-MAML2; Ependymoma; Ganglion cell feature; Granular cell feature
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Year: 2020 PMID: 33221956 DOI: 10.1007/s10014-020-00388-6
Source DB: PubMed Journal: Brain Tumor Pathol ISSN: 1433-7398 Impact factor: 3.298