Desmoid tumors located in the abdomen or associated with adenomatous polyposis: French intergroup clinical practice guidelines for diagnosis, treatment, and follow-up (SNFGE, FFCD, GERCOR, UNICANCER, SFCD, SFED, SFRO, ACHBT, SFR).

Date publication

mai 2022

Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver

Auteurs

Membres identifiés du Cancéropôle Est :
Pr BOUCHE Olivier , Pr GANGI Afshin

Tous les auteurs :
Benech N, Bonvalot S, Dufresne A, Gangi A, Le Péchoux C, Lopez-Trabada-Ataz D, Meurgey A, Nicolas N, Orbach D, Penel N, Salas S, Saurin JC, Walter T, Lecomte T, Bouché O, ,,,,,,,,,

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/35508462

Résumé

Desmoid tumor (DT) of the abdomen is a challenging and rare disease. The level of evidence available to document their treatment is relatively low, however, recent publications of prospective studies have allowed to precise their management.

Mots clés

Desmoid tumors, Desmoid-type fibromatosis, Familial adenomatous polyposis, French clinical practice guidelines, Mesenchymal tumors, Soft tissue sarcoma

Référence

Dig Liver Dis. 2022 May 1;: