4.6 Article

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

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FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.754131

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synovial sarcoma; bone tumor; small round cell; poorly differentiated; SYT-SSX fusion gene

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Primary intraosseous poorly differentiated synovial sarcoma is extremely rare. We present a case of this type of sarcoma from the proximal femur in a 16-year-old girl. The case was initially misdiagnosed but eventually confirmed by molecular testing. Recognition of this type of sarcoma composed of small round cells is crucial to avoid misdiagnosis as other types of tumors.
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.

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