Primary cardiac synovial sarcoma —A case report—

1998 ◽  
Vol 46 (9) ◽  
pp. 923-927 ◽  
Author(s):  
Munehiro Fujioka ◽  
Shigefumi Suehiro ◽  
Toshihiko Shibata ◽  
Hiroaki Kinoshita ◽  
Kenichi Wakasa ◽  
...  
2010 ◽  
Vol 61 (3) ◽  
pp. 150-155 ◽  
Author(s):  
Yuki Yokouchi ◽  
Nobuyuki Hiruta ◽  
Toshiaki Oharaseki ◽  
Fumie Ihara ◽  
Yoshinao Oda ◽  
...  

Sarcoma ◽  
2007 ◽  
Vol 2007 ◽  
pp. 1-4 ◽  
Author(s):  
Brian Boulmay ◽  
Gary Cooper ◽  
John D. Reith ◽  
Robert Marsh

Synovial sarcoma comprises approximately 10%of all soft tissue sarcoma diagnoses; a primary synovial sarcoma of the myocardium is exceedingly rare. There have been very few cases reported in the literature thus far. With the identification of the characteristic and diagnostic chromosomal abnormality t(X;18), this may become an increasingly recognized entity. Our report adds to the limited published cases of primary cardiac synovial sarcoma with the characteristic t(X;18). Further elucidation of the effects of this translocation on the cell cycle may lead to directed therapies in the future.


2015 ◽  
Vol 9 (5) ◽  
pp. 1947-1949 ◽  
Author(s):  
HIROAKI SATOH ◽  
NORIO TAKAYASHIKI ◽  
TOSHIHIRO SHIOZAWA ◽  
KUNIHIKO MIYAZAKI ◽  
GEN OHARA ◽  
...  
Keyword(s):  

2021 ◽  
Vol 219 ◽  
pp. 153352
Author(s):  
Yusuke Kuboyama ◽  
Yuichi Yamada ◽  
Kenichi Kohashi ◽  
Yu Toda ◽  
Koji Kawakami ◽  
...  

2021 ◽  
Vol 14 (3) ◽  
pp. e237099
Author(s):  
Daanesh Huned ◽  
Juinn Huar Kam ◽  
Lui Shiong Lee ◽  
Raj Vikesh Tiwari

Synovial sarcomas are most commonly localised in extremities, especially in the lower thigh and knee areas. Comprising less than 1% of all malignancies, retroperitoneal synovial sarcoma is very rare with primary synovial sarcoma of the kidney being even more infrequent and difficult to diagnose. We describe a case report of a renal synovial sarcoma in a young adult who was initially managed as a case of Wunderlich’s syndrome secondary to what was believed to be a ruptured renal angiomyolipoma. After biopsy confirmation, the patient was eventually managed with neo-adjuvant chemotherapy followed by a right radical nephrectomy and right hepatectomy. Despite its rarity, synovial sarcoma should be considered as differential diagnosis of a bleeding retroperitoneal soft tissue mass detected in young adults.


2021 ◽  
Vol 78 ◽  
pp. 270-273
Author(s):  
Charles Marchand Crety ◽  
Sara Bellefqih ◽  
Koceila Amroun ◽  
Christian Garbar ◽  
Felix Felici

2019 ◽  
Vol 17 ◽  
pp. 200314
Author(s):  
Afnan Elsayed ◽  
Haneen Al-Maghrabi ◽  
Hosam Alardati ◽  
Ameen Alherabi ◽  
Abdelrazak Meliti

2013 ◽  
Vol 209 (11) ◽  
pp. 745-750 ◽  
Author(s):  
Shu Sahara ◽  
Yoshiro Otsuki ◽  
Yuki Egawa ◽  
Shin-ichi Shimizu ◽  
Yashiro Yoshizawa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document