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 › peer-review

9 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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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.",

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AU - Sinclair, Tiffany J.

AU - Thorson, Chad M.

AU - Alvarez, Elysia

AU - Tan, Serena

AU - Spunt, Sheri L.

AU - Chao, Stephanie D.

PY - 2017/5/1

Y1 - 2017/5/1

N2 - 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.

AB - 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.

KW - Hereditary cancer syndrome

KW - Li–Fraumeni syndrome

KW - Sarcoma

KW - TP53 mutation

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ER -

Pleomorphic myxoid liposarcoma in an adolescent with Li–Fraumeni syndrome

Abstract

Keywords

ASJC Scopus subject areas

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