Your browser doesn't support javascript.
loading
Genomic Profiling of a Case of Glioneuronal Tumor with Neuropil-like Islands.
Tsuboi, Nobushige; Ishida, Joji; Shimazu, Yosuke; Edaki, Hisanori; Uneda, Atsuhito; Otani, Yoshihiro; Fujii, Kentaro; Kurozumi, Kazuhiko; Ennishi, Daisuke; Yanai, Hiroyuki; Date, Isao.
Afiliação
  • Tsuboi N; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Ishida J; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Shimazu Y; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Edaki H; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Uneda A; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Otani Y; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Fujii K; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
  • Kurozumi K; Department of Neurosurgery, Hamamatsu University School of Medicine.
  • Ennishi D; Center for Comprehensive Genomic Medicine, Okayama University Hospital.
  • Yanai H; Department of Pathology, Okayama University Hospital.
  • Date I; Department of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
Acta Med Okayama ; 76(4): 473-477, 2022 Aug.
Article em En | MEDLINE | ID: mdl-36123163
Glioneuronal tumor with neuropil-like islands (GNTNI) is a very rare subtype of glioneuronal tumor. We present a case of a 62-year-old man with GNTNI. Two adjacent lesions in the left parietal lobe were removed by left parietal craniotomy. The histological findings were glial cell proliferation and scattered rosettes consisting of synaptophysin-positive and NeuN-positive cells, leading to the diagnosis of GNTNI. Target sequencing revealed a genetic alteration similar to glioblastoma, IDH-wild type, which suggested adjuvant therapies. There are few previous reports on the treatment of this disease, and the patient should be followed carefully.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas Limite: Humans / Male / Middle aged Idioma: En Revista: Acta Med Okayama Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas Limite: Humans / Male / Middle aged Idioma: En Revista: Acta Med Okayama Ano de publicação: 2022 Tipo de documento: Article