Desmoid tumor of mesentery in familial adenomatous polyposis: a case report

2010 ◽  
Vol 14 (S1) ◽  
pp. 61-62 ◽  
Author(s):  
G. Basdanis ◽  
V. N. Papadopoulos ◽  
S. Panidis ◽  
I. Tzeveleki ◽  
E. Karamanlis ◽  
...  
2018 ◽  
Vol 90 (3) ◽  
pp. 53-58
Author(s):  
Adam Nałęcz ◽  
Krzysztof Dębski ◽  
Marek Dobosz ◽  
Magdalena Krauze

Desmoid (desmoid tumor) is a cytologically benign fibrous tumor that originates from musculoskeletal structures of the entire body [1]. The term "desmoid", first introduced by Muller in 1838, derives from the Greek word desmos, which means tendinous [2]. The etiopathogenesis of desmoid is not fully understood, most reports of publications regarding its treatment are based on individual case reports. The prognosis is good, and healing is achieved mainly through surgical excision of the lesion. The aim of the paper is to present a case of a 33-year-old woman with diagnosed familial polyposis in the colon, who has been identified with mesenteric desmoid.


2008 ◽  
Vol 24 (1) ◽  
pp. 20 ◽  
Author(s):  
Dae Dong Kim ◽  
Chang Sik Yu ◽  
Dong Hyun Hong ◽  
Sang Hun Jung ◽  
Pyong Wha Choi ◽  
...  

2012 ◽  
Vol 9 (1) ◽  
pp. 32-6 ◽  
Author(s):  
Oktay Algin ◽  
Sehnaz Evrimler ◽  
Evrim Ozmen ◽  
Melike Metin ◽  
Osman Ersoy ◽  
...  

2003 ◽  
Vol 89 (3) ◽  
pp. 331-332 ◽  
Author(s):  
Ugo Marone ◽  
Alfonso Amore ◽  
Luciano Pezzullo ◽  
Nicola Mozzillo

In this paper a case of vast desmoid tumor of the abdominal wall associated with familial adenomatous polyposis is reported. Desmoid tumors represent a particular type of fibrous neoplasms with a higher prevalence in females. They are extremely rare in the sporadic form, while they are found in about 10% of patients affected by familial adenomatous polyposis. Despite their benign histology and the absence of metastatic potential, they can be considered as fibrosarcomas with a low level of malignancy because of their locally invasive nature. The treatment of choice is surgical excision, as wide as possible, aimed at preventing recurrences, which are frequent in this tumor type. The usefulness of complementary therapies such as radiotherapy, hormone or chemotherapy, is not entirely clear.


2008 ◽  
Vol 1 (1) ◽  
pp. 27-29
Author(s):  
Ovais H Malik ◽  
Prem C Nair ◽  
Anup J Karki ◽  
Rowena J Rimes

2015 ◽  
Vol 32 (6) ◽  
pp. 421-425 ◽  
Author(s):  
Adam L. Goldstein ◽  
Revital Kariv ◽  
Joseph M. Klausner ◽  
Hagit Tulchinsky

Aim: This study aims at identifying the risk factors for the development of pre-cancerous pouch and/or cuff adenomas post ileal pouch anal anastomosis (IPAA) in familial adenomatous polyposis patients. Method: We retrospectively studied 59 patients operated at a single medical center during a 26-year period. Data on the timing and location of adenoma recurrence were recorded and possible correlations with patients' gender, age, presence of desmoid tumor, duodenal adenomas, type of anastomosis and number of operation stages were analyzed. Results: Thirty-five (59%) patients had at least one adenoma in either the cuff or the pouch, including 20 with isolated cuff adenomas, 4 with isolated pouch adenomas and 11 patients with adenomas in both the pouch and cuff. There was no significant correlation between gender, age at surgery, type of anastomosis, number of operative stages and the development of pouch or cuff adenomas. Desmoid tumor and pouch adenomas were significantly correlated with cuff adenomas formation. Duodenal adenomas were associated with pouch adenomas. There was some relationship between the development of cuff adenomas and the burden of colonic polyps, as well as the presence of duodenal adenomas. Conclusion: Adenomas in both the pouch and cuff commonly occur following IPAA, mandating lifelong annual endoscopic surveillance.


2015 ◽  
Vol 9 (1) ◽  
Author(s):  
Nicola Carlomagno ◽  
Francesca Duraturo ◽  
Maria Candida ◽  
Marina De Rosa ◽  
Valeria Varone ◽  
...  

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