Skip to main content
editorial
. 2024 Aug 21;30(31):3640–3653. doi: 10.3748/wjg.v30.i31.3640

Table 1.

Types of gastric polyps



Frequency
Risk factors
Associated conditions
Age/sex
Location
Size
Symptoms
Endoscopic features
Neoplastic potential
Good
Fundic gland Sporadic 80% Proton-pump inhibitors None Middle age/women Body/fundus < 8 mm Asymptomatic Sessile, smooth surface Very rare
Syndromic Hereditary Familial adenomatous polyposis, MUTHY Early age/no sex difference Body, multiple (> 90%) < 6 mm Asymptomatic Rare
Inflammatory fibroid Rare (< 0.1%) Not known
May be familial, Devon polyposis syndrome-associated with PDGFRA mutation Older (6th-7th decade) (adults/slight predominace in women) Antrum-pylorus Mean size 1-5 cm, up to 9 cm Early satiety or good, sometimes bleeding Sessile, pedunculated, +/- ulcerated Very rare
Ectopic pancreas 0.5%-13% None None Not reported Antrum-prepyloric region Variable Incidental Firm round or oval subepithelial lesion with a central depression Benign, no follow-up needed
Hamartomatous polyp Sporadic 1% Not known - Not reported Anywhere Variable Incidental findings Sessile, differential dx H. pylori Benign
Bad
Hamartomatous Syndromic PJS, Juvenile polyposis syndrome and phosphatase and tensin homolog hamartoma syndrome STK11 (PJS) - - The 0.1-3 cm (PJS) - Lifetime malignancy risk (up to 29%)
Hamartomatous Solitary Gastric inverted Hamartomatous Polyps Common (up to 20%)
Hyperplastic 15% H. pylori, chronic atrophic gastritis Not reported Middle age/no sex difference Antrum (60%), any site, solitary, more common multiple Usually < 2 cm, but up to 12 cm Asymptomatic, incidental findings Smooth or lobulated, sessile or pedunculated Dysplasia 15%, cancer risk < 1%
Adenoma 6%-10% Atrophy, intestinal Metaplasia None Middle age/men (intestinal type) More common, antrum (intestinal type), any site (other types) Variable (few mm to cm) Asymptomatic, anemia, bleeding, rarely obstruction Sessile, pedunculated Depends on size; histology (high-grade dysplasia 30% at 5 years); likely gene-disrupting 3% at 5 years
Gastric neuroendocrine tumors < 2% gastric neoplasm
GNET type 1 80% all G-NET Autoimmune gastritis None Middle age/old Body, fundus Small, multiple Asymptomatic anemia Reddish Low (< 1%), locoregional MTS depends on size, grading and mm propria invasion: 5 years survival 100%
GNET type 2 5% Gastrinoma (multiple endocrine neoplasia type 1) Young Body, fundus Small, multiple Diarrhea, abdominal pain
bleeding from peptic ulcer
Small, yellow, often multiple ulceration Lymph node MTS 30% with good prognosis
Ugly
GNET type 3 The 10%-20% all GNET No predisposing factors None Adults/no sex difference Anywhere, preference antrum Large, solitary Asymptomatic Single lesion The 50% risk MTS. Survival 70% at 5 years
Early gastric cancer Sporadic hereditary
(1%-3%)
Equal to gastric adenomaE-cadherin gene None Adult/old/male Antrum (50%) corpus (35%), cardia (15%) Epigastric pain glycemic index bleeding, anemia, vomiting/nausea Polyp, ulcer The 5 years survival 75%, the 80% lifetime cancer risk

GNET: Gastro-intestinal neuroectodermal tumor; PJS: Peutz-Jeghers syndrome; H. pylori: Helicobacter pylori; MTS: Metastasis.