S6452 From GAVE to Polyps: Is Treatment a Double-Edged Sword?

Introduction: Gastric antral vascular ectasia (GAVE), or “watermelon stomach,” is a rare but important cause of chronic gastrointestinal bleeding and iron deficiency anemia. While commonly associated with portal hypertension and autoimmune diseases, other contributing factors—such as mechanical stress and metabolic syndrome—have been implicated. Aortic stenosis, through Heyde’s syndrome, is also linked to GAVE. Argon plasma coagulation (APC) remains a first-line treatment. We present a unique case of a patient with GAVE who developed numerous hyperplastic gastric polyps after undergoing repeated APC treatments. Case Description/Methods: A 66-year-old woman with a history of bariatric surgery and moderate aortic stenosis presented with recurrent iron deficiency anemia and melena. Initial endoscopy revealed gastric and duodenal hyperplastic polyps along with Helicobacter pylori infection. Over time, she developed active GAVE, managed with multiple APC sessions. Despite therapy, bleeding persisted, and the polyps enlarged progressively. Histology confirmed chronic gastritis and hyperplastic changes, with no evidence of dysplasia. Serum gastrin levels remained within normal range, making hypergastrinemia an unlikely cause of polyp growth. Discussion: This case illustrates an atypical presentation of GAVE in a post-bariatric surgery patient without the common risk factors of portal hypertension or autoimmune disease. Aortic stenosis, possibly through acquired von Willebrand factor deficiency, may underlie the bleeding seen in Heyde’s syndrome. Mechanical stress from altered gastric anatomy and features of metabolic syndrome may also contribute to mucosal injury and GAVE development. A notable aspect of this case is the emergence of diffuse hyperplastic polyps following repeated APC therapy. Although APC is the standard treatment for GAVE, cumulative mucosal injury from repeated ablation may provoke a regenerative response, resulting in hyperplastic polyp formation. These polyps, though benign, may bleed, obstruct, or rarely undergo malignant transformation. The observed temporal association in this case highlights the importance of awareness regarding this potential complication. Regular endoscopic surveillance and timely management of symptomatic or enlarging polyps are essential to minimize bleeding and long-term risks.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001154268.56591.80
Primary Topic
Gastrointestinal Bleeding Diagnosis and Treatment
Type
article
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article

S6452 From GAVE to Polyps: Is Treatment a Double-Edged Sword?

The American Journal of Gastroenterology
Gastrointestinal Bleeding Diagnosis and Treatment
article

S6452 From GAVE to Polyps: Is Treatment a Double-Edged Sword?

article en

Abstract

Introduction: Gastric antral vascular ectasia (GAVE), or “watermelon stomach,” is a rare but important cause of chronic gastrointestinal bleeding and iron deficiency anemia. While commonly associated with portal hypertension and autoimmune diseases, other contributing factors—such as mechanical stress and metabolic syndrome—have been implicated. Aortic stenosis, through Heyde’s syndrome, is also linked to GAVE. Argon plasma coagulation (APC) remains a first-line treatment. We present a unique case of a patient with GAVE who developed numerous hyperplastic gastric polyps after undergoing repeated APC treatments. Case Description/Methods: A 66-year-old woman with a history of bariatric surgery and moderate aortic stenosis presented with recurrent iron deficiency anemia and melena. Initial endoscopy revealed gastric and duodenal hyperplastic polyps along with Helicobacter pylori infection. Over time, she developed active GAVE, managed with multiple APC sessions. Despite therapy, bleeding persisted, and the polyps enlarged progressively. Histology confirmed chronic gastritis and hyperplastic changes, with no evidence of dysplasia. Serum gastrin levels remained within normal range, making hypergastrinemia an unlikely cause of polyp growth. Discussion: This case illustrates an atypical presentation of GAVE in a post-bariatric surgery patient without the common risk factors of portal hypertension or autoimmune disease. Aortic stenosis, possibly through acquired von Willebrand factor deficiency, may underlie the bleeding seen in Heyde’s syndrome. Mechanical stress from altered gastric anatomy and features of metabolic syndrome may also contribute to mucosal injury and GAVE development. A notable aspect of this case is the emergence of diffuse hyperplastic polyps following repeated APC therapy. Although APC is the standard treatment for GAVE, cumulative mucosal injury from repeated ablation may provoke a regenerative response, resulting in hyperplastic polyp formation. These polyps, though benign, may bleed, obstruct, or rarely undergo malignant transformation. The observed temporal association in this case highlights the importance of awareness regarding this potential complication. Regular endoscopic surveillance and timely management of symptomatic or enlarging polyps are essential to minimize bleeding and long-term risks.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 30%
Gastrointestinal Bleeding Diagnosis and Treatment
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S6452 From GAVE to Polyps: Is Treatment a Double-Edged Sword? · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS