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Primary spinal cord gliomas: Pathologic features associated with prognosis.
Tanaka, Yuki; Natsumeda, Manabu; Ohashi, Masayuki; Saito, Rie; Higa, Nayuta; Akahane, Toshiaki; Hashidate, Hideki; Ito, Junko; Fujii, Satoshi; Sasaki, Atsushi; Tanimoto, Akihide; Hanaya, Ryosuke; Watanabe, Kei; Oishi, Makoto; Kawashima, Hiroyuki; Kakita, Akiyoshi.
Afiliação
  • Tanaka Y; Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan.
  • Natsumeda M; Division of Orthopedic Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
  • Ohashi M; Department of Neurosurgery, Brain Research Institute, Niigata University, Niigata, Japan.
  • Saito R; Division of Orthopedic Surgery, Niigata University Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
  • Higa N; Department of Pathology, Brain Research Institute, Niigata University, Niigata, Japan.
  • Akahane T; Department of Neurosurgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Hashidate H; Department of Pathology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Ito J; Center for Human Genome and Gene Analysis, Kagoshima University Hospital, Kagoshima, Japan.
  • Fujii S; Department of Pathology, Niigata City General Hospital, Niigata, Japan.
  • Sasaki A; Department of Pathology, Yokohama City University Hospital, Yokohama, Japan.
  • Tanimoto A; Department of Pathology, Yokohama City University Hospital, Yokohama, Japan.
  • Hanaya R; Department of Molecular Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Watanabe K; Department of Pathology, Saitama Medical University, Saitama, Japan.
  • Oishi M; Department of Pathology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Kawashima H; Center for Human Genome and Gene Analysis, Kagoshima University Hospital, Kagoshima, Japan.
  • Kakita A; Department of Neurosurgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Article em En | MEDLINE | ID: mdl-39074166
ABSTRACT
Primary spinal cord gliomas are rare and are associated with high mortality. Unlike brain tumors, the clinicopathological features of spinal cord gliomas are not well defined. We analyzed clinical, histopathology, and immunohistochemical features and overall survival (OS) of 25 patients with primary spinal cord gliomas treated between 1994 and 2023 at 4 institutions. IDH1 R132H, H3K27M, and p53 were assessed by immunohistochemistry (IHC). Four (16%), 5 (20%), 2 (8%), and 13 (52%) patients were diagnosed as having grades 1, 2, 3, and 4 gliomas according to the World Health Organization (WHO) 2021 classification, respectively. One case (4%), with a circumscribed diffuse midline glioma, H3K27-altered, had a rare molecular profile and could not be graded. IHC demonstrated H3K27M positivity, indicative of H3F3A K27M or HIST1H3B K27M mutation, in 9 (36%) patients. H3K27me3-loss was evident in 13 (52%) patients. In one patient with a grade 1 tumor that showed negative staining for H3K27M and H3K27me3 loss, numbers of EZHIP-positive cells were increased, suggesting diffuse midline glioma, H3K27-altered (WHO grade 4). H3K27me3 loss, frequency of p53 positive cells (≥10%), MIB-1 index (≥10%), and high histopathological grades significantly correlated with poor OS. These results indicate the pathological and immunohistochemical characteristics of primary spinal cord gliomas that impact prognosis.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article