Pleomorphic myxoid liposarcoma in an adolescent with Li–Fraumeni syndrome

Tiffany J. Sinclair, Chad M. Thorson, Elysia Alvarez, Serena Tan, Sheri L. Spunt, Stephanie D. Chao

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

We present the case of a 15-year-old female with a right perineal mass that was found to be pleomorphic myxoid liposarcoma, a recently recognized, rare subtype of liposarcoma. The patient had a strong family history of malignancy and genetic screening revealed a pathogenic TP53 mutation consistent with Li–Fraumeni syndrome.

Original languageEnglish (US)
Pages (from-to)631-635
Number of pages5
JournalPediatric Surgery International
Volume33
Issue number5
DOIs
StatePublished - May 1 2017
Externally publishedYes

Keywords

  • Hereditary cancer syndrome
  • Li–Fraumeni syndrome
  • Sarcoma
  • TP53 mutation

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Surgery

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