Primary intramucosal synovial sarcoma of the sigmoid colon in a patient with a germline mutation in the MSH2 gene: A case report

2020 ◽  
Vol 70 (12) ◽  
pp. 1015-1019
Author(s):  
Yasuyuki Shigematsu ◽  
Kyoko Yamashita ◽  
Manabu Takamatsu ◽  
Taisuke Tanizawa ◽  
Yuki Togashi ◽  
...  
Keyword(s):  
Case Report ◽  
Sigmoid Colon ◽  
Synovial Sarcoma ◽  
Germline Mutation ◽  
Msh2 Gene

An Obscure Colon Dilatation and its Underlying Cause: Case Report and Literature Review

2020 ◽  
pp. 1-5
Author(s):  
Anton Stift ◽  
Kerstin Wimmer ◽  
Felix Harpain ◽  
Katharina Wöran ◽  
Thomas Mang ◽  
...  
Keyword(s):  
Case Report ◽  
Sigmoid Colon ◽  
Immunohistochemical Staining ◽  
Late Onset ◽  
Hirschsprung Disease ◽  
Endoscopic Examination ◽  
Case Presentation ◽  
Idiopathic Megacolon ◽  
History Of ◽  
Cells Of Cajal

Introduction: Congenital as well as acquired diseases may be responsible for the development of a megacolon. In adult patients, Clostridium difficile associated infection as well as late-onset of Morbus Hirschsprung disease are known to cause a megacolon. In addition, malignant as well as benign colorectal strictures may lead to intestinal dilatation. In case of an idiopathic megacolon, the underlying cause remains unclear. Case Presentation: We describe the case of a 44-year-old male patient suffering from a long history of chronic constipation. He presented himself with an obscurely dilated large intestine with bowel loops up to 17 centimeters in diameter. Radiological as well as endoscopic examination gave evidence of a spastic process in the sigmoid colon. The patient was treated with a subtotal colectomy and the intraoperative findings revealed a stenotic stricture in the sigmoid colon. Since the histological examination did not find a conclusive reason for the functional stenosis, an immunohistochemical staining was advised. This showed a decrease in interstitial cells of Cajal (ICC) in the stenotic part of the sigmoid colon. Discussion: This case report describes a patient with an idiopathic megacolon, where the underlying cause remained unclear until an immunohistochemical staining of the stenotic colon showed a substantial decrease of ICCs. Various pathologies leading to a megacolon are reviewed and discussed.

scholarly journals Recurrent pulmonary synovial sarcoma effectively treated with amrubicin: A case report

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

Three cases of synovial sarcoma of gastric wall: A case report and review of the literature

2021 ◽  
Vol 219 ◽  
pp. 153352
Author(s):  
Yusuke Kuboyama ◽  
Yuichi Yamada ◽  
Kenichi Kohashi ◽  
Yu Toda ◽  
Koji Kawakami ◽  
...  
Keyword(s):  
Case Report ◽  
Synovial Sarcoma ◽  
Gastric Wall ◽  
Review Of The Literature

Primary renal synovial sarcoma presenting with a retroperitoneal bleed

2021 ◽  
Vol 14 (3) ◽  
pp. e237099
Author(s):  
Daanesh Huned ◽  
Juinn Huar Kam ◽  
Lui Shiong Lee ◽  
Raj Vikesh Tiwari
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Synovial Sarcoma ◽  
Soft Tissue Mass ◽  
Renal Angiomyolipoma ◽  
Right Hepatectomy ◽  
Tissue Mass ◽  
Biopsy Confirmation ◽  
Synovial Sarcomas ◽  
Neo Adjuvant Chemotherapy

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.

scholarly journals Primary gastric synovial sarcoma: A case report and literature review

2021 ◽  
Vol 78 ◽  
pp. 270-273
Author(s):  
Charles Marchand Crety ◽  
Sara Bellefqih ◽  
Koceila Amroun ◽  
Christian Garbar ◽  
Felix Felici
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Synovial Sarcoma ◽  
Gastric Synovial Sarcoma

scholarly journals Synovial sarcoma of submandibular gland with aberrant P63 expression a case report of rare event

2019 ◽  
Vol 17 ◽  
pp. 200314
Author(s):  
Afnan Elsayed ◽  
Haneen Al-Maghrabi ◽  
Hosam Alardati ◽  
Ameen Alherabi ◽  
Abdelrazak Meliti
Keyword(s):  
Case Report ◽  
Submandibular Gland ◽  
Synovial Sarcoma ◽  
Rare Event

Primary synovial sarcoma of the stomach—A case report and review of the literature

2013 ◽  
Vol 209 (11) ◽  
pp. 745-750 ◽  
Author(s):  
Shu Sahara ◽  
Yoshiro Otsuki ◽  
Yuki Egawa ◽  
Shin-ichi Shimizu ◽  
Yashiro Yoshizawa ◽  
...  
Keyword(s):  
Case Report ◽  
Synovial Sarcoma ◽  
Review Of The Literature

Endoscopic removal of an impacted barolith at the sigmoid colon: a rare case report

2017 ◽  
Vol 10 (4) ◽  
pp. 361-363 ◽  
Author(s):  
Tomoya Iida ◽  
Takehiro Hirano ◽  
Kei Onodera ◽  
Toshiyuki Kubo ◽  
Kentaro Yamashita ◽  
...  
Keyword(s):  
Case Report ◽  
Sigmoid Colon ◽  
Rare Case ◽  
Endoscopic Removal ◽  
Rare Case Report
Sign in / Sign up

Export Citation Format

Share Document