A primary primitive neuroectodermal tumor of the central nervous system in a 51-year-old woman: a case report and literature review

Medicina (Kaunas). 2011;47(8):440-5. Epub 2011 Nov 18.

Abstract

Primitive neuroectodermal tumors are a group of rare, aggressive, and highly malignant embryonal tumors of unknown etiology of the central and peripheral nervous systems. It is a term for a group of small round cell tumors thought to be derived from fetal neuroectodermal precursor cells. Primitive neuroectodermal tumor is usually described as a tumor of children younger than 15 years and is very rare in adults. The article presents a short literature review and a rare case of a primary primitive neuroectodermal tumor of the central nervous system diagnosed in a 51-year-old woman.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Brain Neoplasms / diagnosis*
  • Brain Neoplasms / genetics
  • Brain Neoplasms / pathology
  • Cyclin-Dependent Kinase Inhibitor p16 / genetics
  • Exons
  • Female
  • Gene Deletion
  • Homozygote
  • Humans
  • Magnetic Resonance Imaging
  • Middle Aged
  • Neuroectodermal Tumors, Primitive / diagnosis*
  • Neuroectodermal Tumors, Primitive / genetics
  • Neuroectodermal Tumors, Primitive / pathology
  • Tumor Suppressor Protein p14ARF / genetics

Substances

  • Cyclin-Dependent Kinase Inhibitor p16
  • Tumor Suppressor Protein p14ARF