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May 19, 2021 · Synovial sarcomas (SS) represent a unique subset of soft tissue sarcomas (STS) and account for 5–10% of all STS. Synovial sarcoma differs from other STS by the relatively young age at diagnosis and clinical presentation.
- Aaron M. Gazendam, Snezana Popovic, Sohaib Munir, Naveen Parasu, David Wilson, Michelle Ghert
- 10.3390/curroncol28030177
- 2021
- Curr Oncol. 2021 Jun; 28(3): 1909-1920.
May 19, 2021 · Synovial sarcoma (SS) is an infrequent, highly malignant mesenchymal tumor, accounting for approximately 5-10% of all soft tissue sarcomas [1]. The peak incidence of SS occurs between 30 and 40...
Aug 23, 2023 · Synovial sarcoma (SS) is a rare and malignant tumor of the connective tissues that presents challenges in diagnosis and treatment. 1,2 This article describes the epidemiology, clinical and genomic characteristics of SS, and the patient pathway from diagnosis to treatment.
- 10.1016/j.esmoop.2023.101618
- 2023/10
- ESMO Open. 2023 Oct; 8(5): 101618.
Mar 7, 2018 · Synovial sarcoma (SS) is a rare, yet highly malignant, type of soft tissue sarcoma (STS), for which survival has not improved significantly during the past years. In this review, we focus on systemic treatment in adults. Compared to other STS, SS are relatively chemosensitive.
- Ingrid M. E. Desar, Emmy D. G. Fleuren, Winette T. A. van der Graaf
- 2018
May 19, 2021 · Synovial sarcomas (SS) represent a unique subset of soft tissue sarcomas (STS) and account for 5-10% of all STS. Synovial sarcoma differs from other STS by the relatively young age at diagnosis and clinical presentation.
- Aaron M. Gazendam, Snezana Popovic, Sohaib Munir, Naveen Parasu, David Wilson, Michelle Ghert
- 2021
Synovial sarcoma (SyS) is a rare soft tissue sarcoma3 that occurs mostly in adolescents and young adults, accounting for about 5–10% of soft tissue sarcomas. A commonly believed etiological cause for SyS is a chromo-some abnormality known as T (x; 18) (P11.2; q11.2), which results in the formation of SS18-SSX Fusion oncogenes.
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May 19, 2021 · Synovial sarcomas (SS) represent a unique subset of STS and account for 5–10% of all STS. Synovial sarcoma differs from other STS by the relatively young age at diagnosis, anatomic location (peri-articular) and clinical presentation (slow-growing, painful lesions).
