Case Report: Primary Intraosseous Poorly Differentiated Synovial Sarcoma of the Femur

被引:5
作者
Pang, Ke [1 ,2 ]
Guo, Xiaoning [1 ]
Jiang, Yi [3 ]
Xu, Lina [3 ]
Ling, Lin [1 ]
Li, Zhihong [1 ,2 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Orthoped, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Hunan Key Lab Tumor Models & Individualized Med, Changsha, Peoples R China
[3] Cent South Univ, Xiangya Hosp 2, Dept Pathol, Changsha, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
synovial sarcoma; bone tumor; small round cell; poorly differentiated; SYT-SSX fusion gene; ROUND-CELL TUMORS; PRIMITIVE NEUROECTODERMAL TUMORS; MR-IMAGING FINDINGS; EWINGS-SARCOMA; SOFT-TISSUE; IMMUNOHISTOCHEMICAL DETECTION; TLE1; EXPRESSION; BONE; DIAGNOSIS; GENE;
D O I
10.3389/fonc.2022.754131
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Primary intraosseous poorly differentiated synovial sarcoma is exceedingly rare. Here, we present a case of primary intraosseous poorly differentiated synovial sarcoma from the proximal femur in a 16-year-old girl. The case was initially misdiagnosed, but the correct diagnosis of synovial sarcoma was eventually confirmed by fluorescence in situ hybridization and next-generation sequencing. We review the literature pertaining to synovial sarcoma and show that this case is the second molecularly proven intraosseous poorly differentiated synovial sarcoma in the literature. Recognition of intraosseous synovial sarcoma composed of small round cells is imperative in order to avoid misdiagnosis of the tumor as Ewing sarcoma and other small round-cell tumors, all of which have markedly different clinical management.
引用
收藏
页数:12
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