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1. People also ask

   Do sarcomas have visceral metastases?

   • Though isolated visceral metastases from most sarcomas are uncommon [ 29 ], at initial staging inclusion of abdomen and pelvis in the CT is usually performed, especially for myxoid liposarcoma and leiomyosarcoma, and for high-grade sarcomas of the lower extremities.

   UK guidelines for the management of soft tissue sarcomas

   www.nature.com/articles/s41416-024-02674-y

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   How common are soft tissue sarcomas?

   • Soft tissue sarcomas may occur at any age, most often in middle aged and older adults; however, as a proportion of paediatric malignancies they are relatively common comprising 7–10% of all childhood cancers. They are an important cause of death in the 14–29 years’ age group [ 10, 11, 12 ].

   UK guidelines for the management of soft tissue sarcomas

   www.nature.com/articles/s41416-024-02674-y

   See all results for this question

   What sarcomas can be managed at defined anatomical sites?

   • This iteration of the guidance, as well as updating the general multidisciplinary management of soft tissue sarcoma, includes specific sections relating to the management of sarcomas at defined anatomical sites: gynaecological sarcomas, retroperitoneal sarcomas, breast sarcomas, and skin sarcomas.

   UK guidelines for the management of soft tissue sarcomas

   www.nature.com/articles/s41416-024-02674-y

   See all results for this question

2. ascopubs.org › doi › 10Analyzing the effect of treatment modalities on survival in ...

   ascopubs.org › doi › 10

   3 days ago · 11570 Background: Synovial sarcoma (SS) is a rare, slow growing, and aggressive soft tissue sarcoma that commonly affects young adults, with a diagnosis at an average age of 30 years. It usually originates near the joints of the extremities and presents as a painless lump. Metastasis to the regional lymph nodes and lungs is common. SS is proposed to be a result of a chromosomal translocation ...

3. www.mdanderson.org › cancerwise › newest-research-inNewest research in sarcoma | MD Anderson Cancer Center

   www.mdanderson.org › cancerwise › newest-research-in

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   2 days ago · Sarcoma research at MD Anderson goes beyond these presentations at ASCO. For example, Dejka Araujo, M.D., professor of Sarcoma Medical Oncology, and her colleagues recently published findings in The Lancet of a clinical trial of the first T cell therapy for patients with metastatic or unresectable synovial sarcoma or myxoid round cell ...

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5. www.nature.com › articles › s41416/024/02674-yUK guidelines for the management of soft tissue sarcomas - Nature

   www.nature.com › articles › s41416/024/02674-y

   May 11, 2024 · Soft tissue sarcomas (STS) are rare tumours arising in mesenchymal tissues and can occur almost anywhere in the body. Their rarity, and the heterogeneity of subtype and location, means that...

6. www.cureus.com › articles › 248200-synovial-sarcomaCureus | Synovial Sarcoma of the Submaxillary Salivary Gland ...

   www.cureus.com › articles › 248200-synovial-sarcoma

   May 8, 2024 · Synovial sarcoma (SS) is a malignant sarcoma of young adults, rarely involving the head and neck, especially the principal salivary glands. According to Setti et al., soft tissue tumors account for 2-5% of salivary gland tumors [1].

7. link.springer.com › article › 10Underlying synovial sarcoma undiagnosed for more than 20 ...

   link.springer.com › article › 10

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   May 10, 2024 · Synovial sarcoma (SS) is a malignant tumor comprising 5–10% of all soft tissue sarcomas. SS has distinct characteristics, such as a predilection for young adults and relatively slow growth compared to other soft tissue sarcomas.

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     Synovial Sarcoma (explained in 5 minutes): Soft Tissue Pathology Basics

     Aug 30, 2022

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     Synovial Sarcoma 101…Explained by a Soft Tissue Pathologist

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     Synovial Sarcoma: Paige's Mayo Clinic Story

     Mar 4, 2016

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9. www.ncbi.nlm.nih.gov › pmc › articlesSynovial Sarcoma Chromatin Dynamics Reveal a Continuum in ...

   www.ncbi.nlm.nih.gov › pmc › articles

   May 14, 2024 · Synovial sarcoma (SyS) is an aggressive soft-tissue malignancy characterized by a pathognomonic chromosomal translocation leading to the formation of the SS18::SSX fusion oncoprotein. SS18::SSX associates with mammalian BAF complexes suggesting deregulation of chromatin architecture as the oncogenic driver in this tumour type.

10. ascopubs.org › doi › pdfSarcoma Immunotherapy in Sarcoma: Current Data and Promising ...

    ascopubs.org › doi › pdf

    May 23, 2024 · Sarcoma. Immunotherapy in Sarcoma: Current Data and Promising Strategies. Georgina E. Wood, MD, PhD1; Christian Meyer, MD2; Florent Petitprez, PhD3; and Sandra P. D’Angelo, MD4. DOI https://doi.org/10.1200/EDBK_432234. OVERVIEW. Accepted March 27, 2024 Published May 23, 2024.