Pleomorphic myxoid liposarcoma in an adolescent with Li–Fraumeni syndrome

被引:0
作者
Tiffany J. Sinclair
Chad M. Thorson
Elysia Alvarez
Serena Tan
Sheri L. Spunt
Stephanie D. Chao
机构
[1] Stanford University School of Medicine,Department of Surgery
[2] Stanford University School of Medicine,Division of Pediatric Surgery, Department of Surgery
[3] Stanford University School of Medicine,Division of Pediatric Hematology/Oncology, Department of Pediatrics
[4] Stanford University School of Medicine,Department of Pathology
来源
Pediatric Surgery International | 2017年 / 33卷
关键词
Sarcoma; TP53 mutation; Hereditary cancer syndrome; Li–Fraumeni syndrome;
D O I
暂无
中图分类号
学科分类号
摘要
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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页码:631 / 635
页数:4
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