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Ménétrier disease: A clinical review
Ana R Barros1, Sara Monteiro2, Jorge Silva2
1Department of Gastroenterology, Unidade Local de Saúde Tâmega e Sousa, Penafiel 4560-136, Porto, Portugal. anaritambarros@gmail.com.
Ménétrier disease (MD) causes enlarged stomach folds and protein loss. Treatment ranges from medication to surgery, with targeted therapies showing promise for this rare gastric disorder.
Area of Science:
- Gastroenterology
- Pathology
Background:
- Ménétrier disease (MD), or hyperplastic hypersecretory gastropathy, is a rare gastric disorder.
- Characterized by gastric mucosal hypertrophy, giant folds, excessive mucus, and protein loss.
Purpose of the Study:
- To review the current understanding of Ménétrier disease.
- To outline diagnostic approaches and therapeutic strategies for MD.
Main Methods:
- Literature review of MD pathogenesis, clinical presentation, diagnosis, and treatment.
- Analysis of studies linking MD to EGFR signaling.
Main Results:
- MD pathogenesis involves excessive transforming growth factor-alpha signaling via EGFR.
- Clinical features include epigastric pain, weight loss, and edema.
- Diagnosis relies on clinical, endoscopic, and histopathological findings.
Conclusions:
- MD requires a comprehensive approach to diagnosis and management.
- Targeted therapies like EGFR inhibitors offer new treatment avenues.
- Further research into MD pathogenesis is warranted.
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