Gastric Polyps
Basics
Basics
Basics
Mucosal lesions projecting above the gastric surface and into the lumen of the stomach
Description
Description
Description
- Mostly benign with minimal malignant potential
- Most commonly discovered as asymptomatic incidental findings on upper endoscopy (esophagogastroduodenoscopy [EGD])
- Different types based on origin:
- Epithelial (most common): fundic gland, hyperplastic, adenomas
- Endocrine: carcinoid tumors
- Infiltrative: xanthomas and lymphoid proliferations
- Mesenchymal: gastrointestinal stromal tumor (GIST), leiomyoma, fibroma, lipoma
- Inflammatory fibroid polyp
Epidemiology
Epidemiology
Epidemiology
Incidence
- Incidence ~6% in the United States (1)
- Male = female (1:1)
- Frequency of polyp types:
- Fundic gland: 13–77%
- Hyperplastic: 18–70%
- Adenoma: 0.5–3.75%
- Carcinoid: <2%
- Xanthoma: 0.3–3.9%
- GIST: 1–3%
- Inflammatory fibroid: 0.1–3%
- Hamartomas: <1%
- Others: <1%
Prevalence
Prevalence varies worldwide, estimated to be ~4% in United States. Fundic gland polyps (often arising in the setting of long-term proton pump inhibitor [PPI] use) are the dominant type. Polyps associated with Helicobacter pylori gastritis (hyperplastic and adenomatous) have become less common. Fundic gland polyps represent ~80% of polyps.
Geriatric Considerations
2/3 of gastric polyps are in patients >60 years old.
Pediatric Considerations
Gastric polyps are common in both children and adults with familial adenomatous polyposis (FAP) syndrome. Most often, these are fundic gland polyps.
Etiology and Pathophysiology
Etiology and Pathophysiology
Etiology and Pathophysiology
- Fundic gland polyp
- Sessile lesion usually <0.5 cm; found throughout the stomach
- Most occur sporadically.
- Associated with polyposis syndromes (FAP, MUTYH-associated polyposis [MAP], and gastric adenocarcinoma and proximal polyposis of the stomach [GAPPS])
- Very low risk for malignancy (except in FAP syndrome)
- Associated with long-term PPI use
- Histology shows dilated oxyntic glands, lined by flattened parietal and mucous cells.
- Hyperplastic polyp
- Smooth, rounded (typically multiple) lesions, usually in the antrum
- 0.5 to 1.5 cm—can be much larger
- Hyperregenerative response of epithelium due to chronic inflammation (most commonly H. pylori)
- Low risk for malignancy
- Risk of malignancy in hyperplastic polyps increases with size (>1 cm) and pedunculation.
- Loss of p16 and increased Ki-67 expression may indicate dysplasia in hyperplastic polyps.
- Adenomatous polyp (raised intraepithelial neoplasia)
- Typically associated with chronic atrophic gastritis
- Velvety, lobulated, usually solitary lesion; most often found in the antrum; <2 cm
- Considered to be premalignant
- Malignant potential depends on size (>2 cm with 40–50% risk of malignant transformation) and degree of dysplasia and villous component.
- Carcinoid polyp
- Clusters of mucosal enterochromaffin cells; most often in the corpus or fundus
- Derived from enterochromaffin-like (ECL) cells
- Risk for metastasis depends on size.
- Four distinct subtypes (type 1 most common)
- Xanthoma
- Small, yellow nodules or plaques that protrude from the surrounding pink gastric mucosa
- Lipid-laden macrophages containing cholesterol and neutral fat embedded in the lamina propria
- No malignant potential
- GISTs
- Neoplastic proliferations of interstitial cells of Cajal (or their precursors)
- Well-circumscribed, submucosal lesions; most often in the fundus; median size 6 cm
- Varying malignant potential based on size and mitotic activity
- 50% of patients with GISTs >2 cm have metastatic disease at the time of presentation (usually liver).
- Inflammatory fibroid polyp
- Originates from submucosa; frequently with central depression or ulceration; 1 to 5 cm
- No malignant potential
- Hyperplastic and adenomatous polyps are associated with any inflammatory process causing chronic cell turnover.
- Hamartomas
- Abnormal growth of otherwise normal tissue
- Benign; rarely invade or compress surrounding structures
- All others: no known causes
Genetics
- Most polyps have no known hereditary component.
- Fundic gland polyps are associated with FAP arising from APC gene mutation.
Risk Factors
Risk Factors
Risk Factors
- Increased incidence with age
- Chronic gastritis: hyperplastic polyps
- Chronic NSAID use, increased gastric secretions, erosions, or ulcers
- Hypergastrinemia (gastrinoma, Zollinger-Ellison syndrome, long-term PPI use): fundic gland polyps
- H. pylori: hyperplastic and adenomatous polyps
- BRAF inhibitors used to treat melanoma may increase the risk for hypertrophic gastric polyps.
Commonly Associated Conditions
Commonly Associated Conditions
Commonly Associated Conditions
- Associated with certain familial syndrome (1)[C]
- Fundic gastric polyps: FAP
- Hamartomas: Peutz-Jeghers syndrome, juvenile polyposis, Cronkhite-Canada syndrome, Cowden disease
- Carcinoid polyps:
- Type 1: achlorhydria, hypergastrinemia, and pernicious anemia
- Type 2: Zollinger-Ellison syndrome, MEN1 syndrome
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