Neurospine (Jun 2022)

Recent Molecular and Genetic Findings in Intramedullary Spinal Cord Tumors

  • Yoshitaka Nagashima,
  • Yusuke Nishimura,
  • Kaoru Eguchi,
  • Junya Yamaguchi,
  • Shoichi Haimoto,
  • Fumiharu Ohka,
  • Masakazu Takayasu,
  • Ryuta Saito

DOI
https://doi.org/10.14245/ns.2244168.084
Journal volume & issue
Vol. 19, no. 2
pp. 262 – 271

Abstract

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The study of genetic alterations and molecular biology in central nervous system (CNS) tumors has improved the accuracy of estimations of patient prognosis and tumor categorization. Therefore, the updated 2021 World Health Organization (WHO) classification includes various diagnostic genes, molecules, and pathways for diagnosis, as well as histological findings. These findings are expected both to have diagnostic applications and to facilitate new targeted therapies that target tumor-specific genetic changes and molecular biology. Intramedullary spinal cord tumors (IMSCTs) are rare CNS tumors that are difficult to treat because they occur in eloquent areas. Although the genetic underpinnings of IMSCTs remain unclear compared to their intracranial counterparts, the genetic characteristics of these tumors are gradually being revealed. Here, we describe the major changes in the new 2021 WHO classification and review the major types of IMSCTs, with an emphasis on their clinical features and genetic alterations.

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