Publication details

GAPPS - syndrom adenokarcinomu žaludku a mnohočetné polypózy žaludku v 8 rodinách testovaných v Masarykově onkologickém ústavu – prevence vč. profylaktické gastrektomie

Title in English GAPPS – gastric adenocarcinoma and proximal polyposis of the stomach syndrome in 8 families tested at Masaryk memorial cancer institute – prevention and prophylactic gastrectomies
Authors

FORETOVÁ Lenka NAVRÁTILOVÁ Marie SVOBODA Marek GRELL Peter NĚMEC Libor SIROTEK Lukáš OBERMANNOVÁ Radka NOVOTNÝ Ivo ŠACHLOVÁ Milana FABIAN Pavel KROUPA Radek VAŠÍČKOVÁ Petra HÁZOVÁ Jana HRABINCOVÁ SŤAHLOVÁ Eva MACHÁČKOVÁ Eva

Year of publication 2019
Type Article in Periodical
Magazine / Source Klinická onkologie
MU Faculty or unit

Faculty of Medicine

Citation
Web https://www.linkos.cz/english-summary/klinicka-onkologie-journal/2019-08-18-supplementum-2-en/gapps-syndrom-adenokarcinomu-zaludku-a-mnohocetne-polypozy-zaludku-v-8-rodinach-1/
Doi http://dx.doi.org/10.14735/amko2019S109
Keywords Gastrectomy; Gastric; Gastric cancer; Hereditary; Polyposis
Description Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) is a rare variant of familial adenomatous polyposis. It is an autosomal-dominant cancer-predisposition syndrome with massive polyposis of the stomach and a significant risk of gastric adenocarcinoma. Li et al., 2016, described point mutations in the Ying Yang 1 binding site of the APC gene 1B promoter associated with GAPPS syndrome. The first GAPPS syndrome in a Czech family was described in 2016. At Masaryk Memorial Cancer Institute, GAPPS syndrome was diagnosed in eight families using Sanger sequencing. In all families, one mutation in promoter 1B of APC gene NM_001127511: C.-191T>C was detected. This mutation was not found in any patient with multiple colon polyposis without a detected classic mutation in the APC gene. In total, 24 carriers of this mutation in promoter 1B of the APC gene were detected. Out of those 24 carriers, 20 had massive gastric polyposis with more than 100 fundic glandular polyps diagnosed between the age of 22 and 65, 5 had already died of adenocarcinoma of the stomach (at the ages of 29, 40, 59, 60 and 64, respectively) and another woman was treated at the age of 29. Two female carriers do not yet have polyposis of the stomach at the ages of 31 and 65, respectively; one female carrier has incipient polyposis at the age of 58. A male carrier does not have any clinical symptoms, gastroscopy was not indicated because of his age. Prophylactic total gastrectomy with D2 lymphadenectomy has already been performed 6 times at Masaryk Memorial Cancer Institute, in 5 cases without adenocarcinoma at the ages of 27, 34, 44, 51 and 66, respectively; in one female carrier adenocarcinoma of the stomach was detected in a histology specimen. Two prophylactic gastrectomies with D1 lymphadenectomy were performed at University Hospital Brno at the ages of 42 and 50, respectively. In the Czech Republic point mutation c.-191T>C (rs879253783) in the 1B promoter of the APC gene is a frequent cause of gastric polyposis with a high risk of gastric adenocarcinoma, even at a young age. Positively tested individuals are recommended to high-risk oncology clinic. A necessary part of the discussion with the patient is information about a preventive gastrectomy.