Abstract

A 13 years old girl admitted due to epigastric pain. She had a history of osteoid osteoma operation and a cousin diagnosed as familial adenomatosis polyposis. She was found to have polypoid structures beginning from antrum to the end of the first part of duodenum at gastroduodenoscopy which are reported as parietal hyperplasia. Her complaints were increased with proton pump inhibitor treatment and two more gastroduodenoscopy were needed to be diagnosed as Menetrier's disease. No etiologic factor could be demonstrated. She's been followed for the last year.

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