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Brunner's gland hamartomas: Not always benign
Manar Shmais1, Ahmad Mousawi2, Fadi Mourad2
1Division of Gastroenterology and Hepatology, Saint Louis University Hospital, MO, USA.
Brunner's gland hamartoma (BGH) is a rare duodenal tumor. While often asymptomatic, BGH can cause serious complications like bleeding or high-grade dysplasia, necessitating medical intervention.
Area of Science:
- Gastroenterology
- Surgical Pathology
Background:
- Brunner's gland hamartoma (BGH) is a rare, benign duodenal tumor, often incidentally discovered during esophagogastroduodenoscopy (EGD).
- While typically asymptomatic, BGH can manifest with significant complications such as anemia, gastrointestinal bleeding, obstruction, or dysplasia.
Approach:
- This report details two cases of large duodenal BGHs.
- One case presented with severe gastrointestinal bleeding.
- The second case, identified during EGD for iron deficiency anemia, revealed high-grade dysplasia.
Key Points:
- Brunner's gland hamartomas, though rare, can present with severe clinical manifestations.
- Complications include iron deficiency anemia, overt gastrointestinal bleeding, and the potential for malignant transformation.
- Prompt diagnosis and management are crucial for patients with symptomatic BGH.
Conclusions:
- Brunner's gland hamartomas require careful evaluation due to their potential for serious complications.
- The malignant potential of BGH, although low, underscores the importance of vigilance and appropriate resection when indicated.
- This review highlights the spectrum of BGH complications and their management implications.
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