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The Epidemiology of Brain and Spinal Cord Tumors Publisher Pubmed



Shobeiri P1, 4 ; Seyedmirzaei H1, 4 ; Kalantari A1, 4 ; Mohammadi E2 ; Rezaei N1, 4 ; Hanaei S3, 4
Authors
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Authors Affiliations
  1. 1. Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Pediatric Neurosurgery, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Neurosurgery, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  4. 4. Universal Scientific Education and Research Network (USERN), Tehran, Iran

Source: Advances in Experimental Medicine and Biology Published:2023


Abstract

CNS tumors are a diverse group of neoplasms that emerge from a variety of different CNS cell types. These tumors may be benign, malignant, or borderline in nature. The majority of high grade glial tumors are fatal, with the exception of pilocytic astrocytoma. Primary malignant CNS tumors occur at a global annual rate of 2.1 to 5.8 per 100,000 persons. Males are more likely to develop malignant brain tumors than females, whereas benign meningiomas are more common in adult females. Additionally, gender inequalities in non-malignant tumors peak between the ages of 25 and 29 years. Only a small number of genetic variants have been associated with survival and prognosis. Notably, central nervous system (CNS) tumors exhibit significant age, gender, and race variation. Race is another factor that affects the incidence of brain and spinal cord tumors. Different races exhibit variation in terms of the prevalence of brain and CNS malignancies. This chapter discusses ongoing research on brain and spinal cord tumor epidemiology, as well as the associated risks and accompanied disorders. © 2023, The Author(s), under exclusive license to Springer Nature Switzerland AG.
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