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Clinical heterogeneity of desmoplastic infantile ganglioglioma: A case series and literature review

  • Trent R. Hummel
  • , Lili Miles
  • , Francesco T. Mangano
  • , Blaise V. Jones
  • , James I. Geller
  • Cincinnati Children's Hospital Medical Center
  • Laboratory Medicine

Research output: Contribution to journal › Review article › peer-review

27 Scopus citations

Abstract

Desmoplastic infantile gangliogliomas (DIG) are intracranial tumors described in 1987 as benign lesions of infancy. A literature review and the clinical course of 3 patients reported herein suggest that the initial description should be amended. Nearly 23% of DIG cases occur in children older than 24 months. Approximately 40% of DIG cases require additional medical, radiation, and/or further surgical intervention, and 15% of infants and children develop leptomeningeal spread or die from DIG. Such adverse outcomes, combined with the recognition that DIG represents a heterogeneous disease, underscore the need for an expanded biological and molecular investigation.

Original languageEnglish
Pages (from-to)e232-e236
JournalJournal of Pediatric Hematology/Oncology
Volume34
Issue number6
DOIs
StatePublished - Aug 2012
Externally publishedYes

Keywords

  • brain tumor
  • cancer
  • desmoplastic infantile ganglioglioma
  • pediatric

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