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Case Report
Retroperitoneal Synovial Sarcoma Manifested by Obstructive Jaundice in an Elderly Woman: Case Report
Dae Ho Kim, Kwang Ro Joo, Jae Myung Cha, Hyun Phil Shin, Joung Il Lee, Jae Jun Park, Hyun Soo Kim, Dal Mo Yang
Clin Endosc 2012;45(4):428-430.   Published online November 30, 2012
DOI: https://doi.org/10.5946/ce.2012.45.4.428
AbstractAbstract PDFPubReaderePub

Synovial sarcoma is a rare type of soft tissue sarcoma that arises in tissues containing synovial fluid, usually in the extremities. It has only rare occurrence in the retroperitoneal space. Early detection of retroperitoneal synovial sarcoma is difficult, since the retroperitoneal space is highly expandable and deeply hidden. Furthermore, the presenting symptoms are often vague and nonspecific, and are related to the pressure on adjacent structures. In this study, we present an unusual case of retroperitoneal synovial sarcoma with obstructive jaundice due to intrabiliary blood clots caused by invasion of bile duct by tumor. The obstructive jaundice was relieved through endoscopic removal of the blood clots and insertion of a biliary stent.

Citations

Citations to this article as recorded by  
  • Primary retroperitoneal synovial sarcoma (RSS): A case report
    Sarra Ben Rejeb, Safia Sakly, Majdi Ben Romdhane, Mehdi Charfi, Adnen Chouchen
    International Journal of Surgery Case Reports.2025; 127: 110982.     CrossRef
  • Management of primary retroperitoneal synovial sarcoma: A case report and review of literature
    Aikaterini Mastoraki, Dimitrios Schizas, Ioannis S Papanikolaou, George Bagias, Nikolaos Machairas, George Agrogiannis, Theodore Liakakos, Nikolaos Arkadopoulos
    World Journal of Gastrointestinal Surgery.2019; 11(1): 27.     CrossRef
  • Intrapelvic Retroperitoneal Synovial Sarcoma in a 15-Year-Old Adolescent Girl: A Case Report and Review of the Literature
    Stan A. Bessems, Maarten van Heinsbergen, Paul H. Nijhuis, Kees C.P. van de Ven, Frits Aarts
    Journal of Pediatric Hematology/Oncology.2019; 41(8): 627.     CrossRef
  • Primary Monophasic Synovial Sarcoma of the Liver in a 13-Year-Old Boy
    Bo Xiong, Min Chen, Feng Ye, Zhuxue Zhang, Lijuan Yin, Huifen Huang, Huijiao Chen, Hongying Zhang
    Pediatric and Developmental Pathology.2013; 16(5): 353.     CrossRef
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A Case of Metastatic Gastric Synovial Sarcoma
Yong Leul Oh, M.D., Yoon Tae Jeen, M.D., Yong Sik Kim, M.D., Rok Son Choung, M.D., Young Sun Kim, M.D., Chul Hee Park, M.D., Hoon Jai Chun, M.D., Hong Sik Lee, M.D., Sang Woo Lee, M.D., Soon Ho Um, M.D., Jai Hyun Choi, M.D., Chang Duck Kim, M.D., Ho Sang
Korean J Gastrointest Endosc 2003;27(6):536-540.   Published online December 30, 2003
AbstractAbstract PDF
Synovial sarcomas are malignant soft tissue neoplasms that develop from tendon and bursa near the large joints and frequently occur in the lower extremities of young male adults. They usually recur within 2 years after surgical treatment. The lung is a common metastatic site and rarely reported as the primary site of synovial sarcoma. The stomach is a very rare primary site of synovial sarcoma and recently only two cases of primary gastric synovial sarcoma were reported. We report a case of metastatic gastric synovial sarcoma in a 53-year-old male 4 years after surgical treatment of primary lung synovial sarcoma. The tumor had histologic, immunohistochemical and ultrastructural features of biphasic synovial sarcoma of the soft tissue. (Korean J Gastrointest Endosc 2003;27:536⁣540)
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  • 9 Download
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