Giant desmoid tumor of the abdominal wall in a patient with Gardner Syndrome

Autor: Guilherme Sousa Sarmento Valente, Matheus Matta Machado Mafra Duque Estrada Meyer, Juliano Alves Figueiredo, Daniel Paulino Santana, Paula Mendonça Pimenta Ferreira, Marcos Wanderley Campos Reis

Publikováno v: Journal of Coloproctology (Rio de Janeiro) v.32 n.3 2012
Journal of Coloproctology (Rio de Janeiro. Online)
Sociedade Brasileira de Coloproctologia (SBCP)
instacron:SBCP
Journal of Coloproctology (Rio de Janeiro), Volume: 32, Issue: 3, Pages: 316-320, Published: SEP 2012
Journal of Coloproctology, Vol 32, Iss 3, Pp 316-320 (2012)

Gardner syndrome (GS) is a rare entity characterized by a triad of familial colonic polyposis, multiple osteomas and soft tissue tumors, including desmoid tumor (DT). This is a case report of a 30 year-old patient with GS who developed giant DT in th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1d36388c6b2009e9f198baf2f619b27
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2237-93632012000300018