Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision

Zaffaroni, G; Mannucci, Alessandro; Koskenvuo, Laura; Borja de Lacy, F.; Maffioli, Anna; M. Bisseling, Tanya; Half, Elizabeth; Martina Cavestro, Giulia; Valle, Laura; Ryan, Neil; Aretz, Stefan; Brown, Karen; Buttitta, Francesco; Carneiro, Fátima; Claber, Oonagh; Blanco‐Colino, Ruth; Collard, M.; J. Crosbie, Emma; Arcanjo Porto da Cunha, Miguel; Doulias, Triantafyllos; Fleming, Christina; Heinrich, Henriette; Hüneburg, Robert; Metras, Julie; D. Nagtegaal, Irıs; Negoi, Ionuţ; Nielsen, Maartje; Pellino, Gianluca; Ricciardiello, Luigi; Sagir, Abdurrahman; Sánchez‐Guillén, Luis; T. Seppälä, Toni; Siersema, Peter; Striebeck, Benedikt; R. Sampson, Julian; Latchford, Andrew; Parc, Yann; Burn, John; Möslein, Gabriela

doi:10.1093/bjs/znae070

Public

Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision

Published in British journal of surgery • Apr 8, 2024

Authors:

G Zaffaroni

Alessandro Mannucci

Laura Koskenvuo

Abstract

BACKGROUND: Hereditary adenomatous polyposis syndromes, including familial adenomatous polyposis and other rare adenomatous polyposis syndromes, increase the lifetime risk of colorectal and other cancers. METHODS: A team of 38 experts convened to update the 2008 European recommendations for the clin...

Subject

Medicine

Familial adenomatous polyposis

MUTYH

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