Results 1 to 10 of about 29,167 (232)
Case Report: Primary Intraosseous Poorly Differentiated Synovial Sarcoma of the Femur
Frontiers in Oncology, 2022 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.
Ke Pang +7 more
doaj +1 more source
Frontiers in Oncology, 2023 Synovial sarcoma is a soft tissue sarcoma accounting for approximately 1,000 cases per year in the United States. Currently, standard treatment of advanced and metastatic synovial sarcoma is anthracycline-based chemotherapy.
Joseph R. Fuchs +3 more
doaj +1 more source
Abdominal Wall Synovial Sarcoma, a Rare Presentation
Case Reports in Clinical Practice, 2022 Synovial sarcoma is a malignant mesenchymal neoplasm which com- monly arises in the extremities of adults, in close association with joint capsules. Only a few cases of synovial sarcoma occurring in the abdominal wall have been reported.
Elham Nazar +2 more
doaj +1 more source
Diagnostic Pathology, 2022 Background Synovial sarcoma is an uncommon soft tissue tumor of soft tissue, characterized by a specific SS18 rearrangement. It generally manifests as a lesion composed of monomorphic spindle cells and sometimes shows variable epithelial differentiation.
Ying Chen +5 more
doaj +1 more source
Synovial Sarcoma of the Thyroid Gland [PDF]
Clinical and Experimental Otorhinolaryngology, 2011 Primary synovial sarcoma of the thyroid is an extremely rare condition which has only been reported twice in the literature. We herein report a case of highly aggressive and rapidly lethal primary synovial sarcoma of the thyroid.
Chang Hwan Ryu +2 more
doaj +1 more source
Annals of Surgery, 1975 Of 34 cases with synovial sarcoma, the five-year survival rate was 36%. A high local recurrence rate results when local excision is performed. Wide excision which may necessitate amputation is the treatment of choice. Prophylactic and even therapeutic node dissections are ineffective in increasing survival because of the disease.
R E, Gerner, G E, Moore
openaire +5 more sources
Accuration of Fine Needle Aspiration Biopsy in Musculoskeletal Tumour [PDF]
, 2016 Fine needle aspiration biopsy (FNAB) has been reported to be the preferable choice of biopsy for musculoskeletal tumour. While FNAB appears to have advantages to core biopsy in the aspect of simplicity and cost, the diagnostic accuracy should be the most
Dewo, P. (Punto) +3 more
core +4 more sources
Case report of intra-articular synovial sarcoma in the hip joint
Radiology Case Reports, 2020 Synovial sarcoma is a type of soft tissue sarcoma that commonly occurs around large joints. However, primary intra-articular synovial sarcoma is considered an extremely rare variant of synovial sarcoma.
Yasser Asiri, MBBS +3 more
doaj +1 more source
Retroperitoneal synovial sarcoma presenting as paraneoplastic hypoglycaemia [PDF]
Journal of Clinical and Scientific Research, 2015 Synovial sarcoma is a well-recognized malignant mesenchymal neoplasm. Primary retroperitoneal synovial sarcoma is extremely rare and has poor prognosis. There are sparse reports in the literature on the secretory synovial sarcomas.
Reddy VV +4 more
doaj +1 more source
Targeting EZH2-mediated methylation of H3K27 inhibits proliferation and migration of Synovial Sarcoma in vitro. [PDF]
, 2016 Synovial sarcoma is an aggressive soft tissue sarcoma genetically defined by the fusion oncogene SS18-SSX. It is hypothesized that either SS18-SSX disrupts SWI/SNF complex inhibition of the polycomb complex 2 (PRC2) methyltransferase Enhancer of Zeste ...
Choy, Edwin +6 more
core +2 more sources