scholarly journals Mesenteric Fibromatosis: A Case Report

2020 ◽  
Vol 17 (3) ◽  
Author(s):  
Hamri Asma ◽  
Samlali Abderrahim ◽  
Daoudi Badre ◽  
Narjis Youssef ◽  
Benelkhaiat Ridouan ◽  
...  
1998 ◽  
Vol 13 (4) ◽  
pp. 383-386 ◽  
Author(s):  
YI-JEN CHEN ◽  
KA-WAI TAM ◽  
CHING-SHYANG CHEN ◽  
CHIH-HSIUNG WU ◽  
SOUL-CHIN CHEN ◽  
...  

2015 ◽  
Vol 87 (9) ◽  
Author(s):  
Radhika Vidyasagar ◽  
Sudarshan ◽  
Sreedhar ◽  
Subramanya ◽  
Vidya Bhat

AbstractMesenteric fibromatosis is a part of the clinical-pathologic spectrum of deep fibromatoses. We report this rare case of primary mesenteric tumor that was diagnosed to be a mesenteric fibromatosis on histopathological examination.In majority of patients it may remain asymptomatic and the management of these tumors depends on histopathological examination. Postoperatively, patient was well and subsequent follow up showed normal recovery.


2005 ◽  
Vol 91 (6) ◽  
pp. 552-554 ◽  
Author(s):  
Pierluigi Ballardini ◽  
Loretta Gulmini ◽  
Guido Margutti ◽  
Giorgio Lelli

Mesenteric fibromatosis is a rare type of desmoid tumor characterized by local aggressiveness and a tendency to relapse. In view of these characteristics it may be considered a low-grade fibrosarcoma. Camurati-Engelmann disease is a very rare form of bone dysplasia characterized by osteosclerosis of the diaphyses of the long bones. Here we describe the case of a male patient affected by these two rare diseases in association with chronic inflammatory intestinal disease.


2010 ◽  
Vol 21 (2) ◽  
pp. 193-195 ◽  
Author(s):  
Semin AYHAN ◽  
Peyker TEMIZ ◽  
Kamile KURT

2002 ◽  
Vol 35 (3) ◽  
pp. 327-331
Author(s):  
Hiroshi Banno ◽  
Hitoshi Kubota ◽  
Toshio Uematsu ◽  
Yutaka Kuroyanagi ◽  
Hideaki Suzuki ◽  
...  

2020 ◽  
Vol 8 (3) ◽  
pp. 577-586
Author(s):  
Huai-Jie Cai ◽  
Han Wang ◽  
Nan Cao ◽  
Wei Wang ◽  
Xi-Xi Sun ◽  
...  

2012 ◽  
Vol 112 (5) ◽  
pp. 386-389
Author(s):  
C.N. Stoidis ◽  
C.N. Spyropoulos ◽  
E.P. Misiakos ◽  
C.K. Fountzilas ◽  
P.P. Paraskeva ◽  
...  

2012 ◽  
Vol 75 (S1) ◽  
pp. 131-133 ◽  
Author(s):  
Geeta karbeet Radhakrishna ◽  
P. R. Bhat ◽  
Rajgopal K. Shenoy ◽  
Srinivas Pai ◽  
Harpreet Singh

2020 ◽  
Vol 11 (S1) ◽  
pp. 73-77
Author(s):  
Abhinav Deshpande ◽  
Ankita Tamhane ◽  
Y. S. Deshpande ◽  
Radhika Pagey ◽  
Meena Pangarkar

Abstract Introduction Mesenteric fibromatosis-desmoid tumor of mesentery is a rare benign soft tissue tumor of mesentery. On CT, it mimics gastrointestinal stromal tumor (GIST). Case Report A 44-year-old female with small intestinal mass, preoperatively diagnosed radiologically and pathologically as GIST. Conclusion Mesenteric fibromatosis is a rare tumor often mistaken for GIST. Histopathology and immunohistochemistry is the key as management of both the tumors differs.


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