Medulloepithelioma with peculiar clinical presentation, stem cell phenotype and aberrant DNA-methylation profile

CNS Oncol. 2015;4(4):203-12. doi: 10.2217/cns.15.9. Epub 2015 Jun 29.

Abstract

We present a 21-year-old male with a neck mass diagnosed as medulloepithelioma. Despite aggressive chemo- and radio-therapy, the tumor metastasized and proved fatal after seventeen months. The tumor demonstrated robust immunohistochemical expression of multiple markers of embryonic/neural stem cells and embryogenesis from the paraffin embedded tissue. The tumor, expressing LIN28A but negative for the 19q13.42 amplicon, also lacked the characteristic methylation profile for medulloepithelioma and other tumors with similar morphology. The expression of embryonic markers may explain its unresponsiveness to therapy and poor prognosis. Therapies targeted at embryonic cell phenotypes may hold the key for successfully treating cancers with embryonal phenotypes or tumors harboring cells with embryonal phenotypes.

Keywords: DNA methylation; ETMR; LIN28A; embryonic stem cells; medulloepithelioma.

Publication types

  • Case Reports

MeSH terms

  • DNA Copy Number Variations
  • DNA Methylation*
  • Fatal Outcome
  • Head and Neck Neoplasms / diagnosis
  • Head and Neck Neoplasms / genetics*
  • Head and Neck Neoplasms / pathology*
  • Head and Neck Neoplasms / therapy
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Neoplastic Stem Cells / pathology*
  • Neuroectodermal Tumors, Primitive / diagnosis
  • Neuroectodermal Tumors, Primitive / genetics*
  • Neuroectodermal Tumors, Primitive / pathology*
  • Neuroectodermal Tumors, Primitive / therapy
  • Tomography, X-Ray Computed
  • Young Adult