S3724 Atypical Polypoidal Lesion Due to Rectal Gastric Heterotopia Presenting as Hematochezia in a Young Adult

Introduction: Gastric heterotopia (GH) is a rare anomaly characterized by the presence of histologically normal gastric mucosa outside its usual location, most commonly found in the esophagus or duodenum. Involvement of the rectum is exceptionally uncommon and can present with rectal bleeding and abdominal pain. Due to the rarity of GH, patients may be misdiagnosed with hemorrhoids, polyps, or other colorectal conditions. We present a case of rectal GH in a 20-year-old man who presented with chronic constipation and hematochezia. Case Description/Methods: A 20-year-old man with history of well controlled HIV on antiretroviral therapy presented to the gastroenterology clinic with a 5-month history of constipation characterized by infrequent, difficult to pass bowel movements, incomplete evacuation, and intermittent hematochezia. The patient denied weight loss, fevers, or nocturnal symptoms and had no significant past medical or surgical history. Dietary history revealed a low-fiber, high-carbohydrate intake. Physical exam was unremarkable. He was initially managed conservatively with polyethylene glycol, methylcellulose, hydration, and dietary modifications for suspected IBS-C. Due to persistent rectal bleeding, a colonoscopy was performed, revealing a 12 mm flat rectal lesion concerning for adenoma or condyloma. The polyp was lifted with saline and en-bloc endoscopic mucosal resection was performed. Histopathology demonstrated rectal mucosa with gastric heterotopia. No adenomatous change or dysplasia was identified. Discussion: Rectal gastric heterotopia is a rare but important differential for unexplained rectal bleeding in young patients. It may lead to symptoms such as local irritation, ulceration, or bleeding from acid secretion by ectopic parietal cells. This case highlights the diagnostic value of colonoscopy in young patients with persistent bleeding, particularly in the immunocompromised, given its broad differential. Histologic evaluation is necessary, as endoscopic appearance may mimic other lesions. While GH is typically benign, surveillance may be considered if symptoms persist or dysplasia develops. This case emphasizes the importance of maintaining a broad differential when evaluating persistent rectal bleeding in young adults. Rectal gastric heterotopia, although rare, should be considered once more common causes are excluded. Colonoscopic evaluation and histopathologic confirmation are essential for accurate diagnosis and management.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001142356.75537.b6
Primary Topic
Gastrointestinal disorders and treatments
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article
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article

S3724 Atypical Polypoidal Lesion Due to Rectal Gastric Heterotopia Presenting as Hematochezia in a Young Adult

Sreeram Parupudi, Jing He, Rebecca Sullivan, Valerie Quach et al.
The American Journal of Gastroenterology
Gastrointestinal disorders and treatments
article

S3724 Atypical Polypoidal Lesion Due to Rectal Gastric Heterotopia Presenting as Hematochezia in a Young Adult

Sreeram Parupudi, Jing He, Rebecca Sullivan, Valerie Quach, Sena Saygili
article en

Abstract

Introduction: Gastric heterotopia (GH) is a rare anomaly characterized by the presence of histologically normal gastric mucosa outside its usual location, most commonly found in the esophagus or duodenum. Involvement of the rectum is exceptionally uncommon and can present with rectal bleeding and abdominal pain. Due to the rarity of GH, patients may be misdiagnosed with hemorrhoids, polyps, or other colorectal conditions. We present a case of rectal GH in a 20-year-old man who presented with chronic constipation and hematochezia. Case Description/Methods: A 20-year-old man with history of well controlled HIV on antiretroviral therapy presented to the gastroenterology clinic with a 5-month history of constipation characterized by infrequent, difficult to pass bowel movements, incomplete evacuation, and intermittent hematochezia. The patient denied weight loss, fevers, or nocturnal symptoms and had no significant past medical or surgical history. Dietary history revealed a low-fiber, high-carbohydrate intake. Physical exam was unremarkable. He was initially managed conservatively with polyethylene glycol, methylcellulose, hydration, and dietary modifications for suspected IBS-C. Due to persistent rectal bleeding, a colonoscopy was performed, revealing a 12 mm flat rectal lesion concerning for adenoma or condyloma. The polyp was lifted with saline and en-bloc endoscopic mucosal resection was performed. Histopathology demonstrated rectal mucosa with gastric heterotopia. No adenomatous change or dysplasia was identified. Discussion: Rectal gastric heterotopia is a rare but important differential for unexplained rectal bleeding in young patients. It may lead to symptoms such as local irritation, ulceration, or bleeding from acid secretion by ectopic parietal cells. This case highlights the diagnostic value of colonoscopy in young patients with persistent bleeding, particularly in the immunocompromised, given its broad differential. Histologic evaluation is necessary, as endoscopic appearance may mimic other lesions. While GH is typically benign, surveillance may be considered if symptoms persist or dysplasia develops. This case emphasizes the importance of maintaining a broad differential when evaluating persistent rectal bleeding in young adults. Rectal gastric heterotopia, although rare, should be considered once more common causes are excluded. Colonoscopic evaluation and histopathologic confirmation are essential for accurate diagnosis and management.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 52%
Gastrointestinal disorders and treatments
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