Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

Frances V. White, Louis P. Dehner, Deborah A Belchis, Katrina Conard, Mary M. Davis, J. Thomas Stocker, Craig W. Zuppan, Jaclyn A. Biegel, Elizabeth J. Perlman

Research output: Contribution to journalArticlepeer-review

Abstract

The clinical, pathologic, and immunohistochemical features of a widely disseminated tumor with rhabdoid phenotype are described in nine infants ≤3 months of age. Five neonates had tumor evident at birth, two of which had placental metastases. The average survival following diagnosis was

Original languageEnglish (US)
Pages (from-to)249-256
Number of pages8
JournalAmerican Journal of Surgical Pathology
Volume23
Issue number3
DOIs
StatePublished - Mar 1999
Externally publishedYes

Keywords

  • Chromosome 22
  • Congenital tumors
  • Malignant rhabdoid tumor
  • Placenta metastasis

ASJC Scopus subject areas

  • Anatomy
  • Pathology and Forensic Medicine

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