Prominent EMA 'dots' in tumour-induced Bergmann gliosis

Histopathology. 2014 Feb;64(3):445-52. doi: 10.1111/his.12260. Epub 2013 Oct 9.

Abstract

Aims: To describe an unusual pattern of epithelial membrane antigen (EMA) immunoreactivity in highly proliferative human Bergmann glia.

Methods and results: An immunohistochemical study was performed of postmortem cerebellar tissue from 18 adult patients with cerebellar damage of various aetiologies and 15 biopsies of diverse adult and paediatric cerebellar tumours. We observed marked proliferation of Bergmann glia with unusual prominent dot-like cytoplasmic EMA immunoreactivity in a case with extensive leptomeningeal sarcomatosis. Similar staining was not observed in association with other types of cerebellar pathology, except for other neoplastic conditions, such as leptomeningeal carcinomatosis, adult medulloblastoma, and pilocytic astrocytoma in children. At an ultrastructural level, the index case showed prominent endoplasmic reticulum with some intermediate filaments and lipofuscin granules, but no structures related to cilia or microvilli were observed.

Conclusions: We consider that prominent EMA dots in Bergmann glia might represent excessive activation induced by an overlying leptomeningeal tumour that stimulates the expression of early developmental antigens. This observation suggests modulation of the glial phenotype when exposed to a neoplastic microenvironment that, in turn, might influence the regenerative potential of Bergmann glia.

Keywords: Bergmann glia; EMA; dots; immunohistochemistry; leptomeningeal sarcomatosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Astrocytoma / metabolism
  • Astrocytoma / pathology
  • Case-Control Studies
  • Cerebellar Neoplasms / metabolism*
  • Cerebellar Neoplasms / pathology*
  • Cerebellum / metabolism
  • Cerebellum / pathology
  • Child
  • Child, Preschool
  • Cytoplasm / metabolism
  • Cytoplasm / pathology
  • Female
  • Gliosis / metabolism*
  • Gliosis / pathology*
  • Humans
  • Immunohistochemistry
  • Infant
  • Male
  • Meningeal Neoplasms / metabolism
  • Meningeal Neoplasms / pathology
  • Middle Aged
  • Mucin-1 / metabolism*
  • Young Adult

Substances

  • MUC1 protein, human
  • Mucin-1