Malignant evolution of choroid plexus papilloma

Edward Chow, Jesse J. Jenkins, Peter C. Burger, David A. Reardon, James W. Langston, Robert A. Sanford, Richard L. Heideman, Larry E. Kun, Thomas E. Merchant

Research output: Contribution to journalArticle

41 Scopus citations

Abstract

Choroid plexus tumors are rare CNS neoplasms. The distinction between choroid plexus papilloma (CPP) and choroid plexus carcinoma (CPC) is made on the basis of clinical and histological criteria. Malignant evolution of CPP may occur, and the presence of mitotic figures in CPP may predict the likelihood of recurrence or malignant evolution. Close surveillance is mandated for these patients. We report on two such cases of CPP that transformed to CPC at the time of recurrence.

Original languageEnglish (US)
Pages (from-to)127-130
Number of pages4
JournalPediatric Neurosurgery
Volume31
Issue number3
DOIs
StatePublished - Sep 1999

Keywords

  • Choroid plexus carcinoma
  • Choroid plexus papilloma
  • Malignant evolution

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Surgery
  • Clinical Neurology

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  • Cite this

    Chow, E., Jenkins, J. J., Burger, P. C., Reardon, D. A., Langston, J. W., Sanford, R. A., Heideman, R. L., Kun, L. E., & Merchant, T. E. (1999). Malignant evolution of choroid plexus papilloma. Pediatric Neurosurgery, 31(3), 127-130. https://doi.org/10.1159/000028847