Low grade ganglioglioma rapidly progressing to a WHO grade IV tumor showing malignant transformation in both astroglial and neuronal cell components

Michel Mittelbronn*, Jens Schittenhelm, Dieter Lemke, Rainer Ritz, Thomas Nägele, Michael Weller, Richard Meyermann, Rudi Beschorner

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

38 Citations (Scopus)

Abstract

Gangliogliomas are rare CNS neoplasms mostly occuring in young adults and are usually assigned to WHO grade I. The few cases of WHO grade IV gangliogliomas were either primarily malignant glio-neuronal tumors or underwent malignant progression from other WHO grades after radiotherapy. Herein, we present the case of a now 47-year-old female patient presenting with a benign ganglioglioma and showing a tumor recurrence 2 years later with an anaplastic ganglioglioma, assigned to WHO grade IV, with malignant transformation in both glial and neuronal components. The presented case is the first reported low-grade ganglioglioma rapidly progressing to a WHO grade IV glio-neuronal tumor not being associated with radiotherapy and showing malignant transformation in both astroglial and neuronal tumor cell components.

Original languageEnglish
Pages (from-to)463-467
Number of pages5
JournalNeuropathology
Volume27
Issue number5
DOIs
Publication statusPublished - Oct 2007
Externally publishedYes

Keywords

  • Anaplastic ganglioglioma
  • Ganglioglioma
  • Malignant progression
  • WHO grade I
  • WHO grade IV

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