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

doi:10.1007/s00383-017-4063-x

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 journal › Article

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 language	English (US)
Pages (from-to)	631-635
Number of pages	5
Journal	Pediatric Surgery International
Volume	33
Issue number	5
DOIs	https://doi.org/10.1007/s00383-017-4063-x
State	Published - May 1 2017
Externally published	Yes

Keywords

Hereditary cancer syndrome
Li–Fraumeni syndrome
Sarcoma
TP53 mutation

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Surgery

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Cite this

Sinclair, T. J., Thorson, C. M., Alvarez, E., Tan, S., Spunt, S. L., & Chao, S. D. (2017). Pleomorphic myxoid liposarcoma in an adolescent with Li–Fraumeni syndrome. Pediatric Surgery International, 33(5), 631-635. https://doi.org/10.1007/s00383-017-4063-x

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