a rare presentation of ménétrier's disease as gastroduodenal intussusception

نویسندگان

mohammad mehdi hayatbakhsh abbasi

sodaif darvish-moqaddam

abdolreza javadi

moeinadin safavi

چکیده

ménétrier's disease is a rare cause of hypertrophic gastropathy that is usually confined to the gastric body and fundus. it is characterized by giant rugae, hypoalbuminemia, and foveolar hyperplasia. here we report the case of a 26-year-old woman who presented with epigastric pain, postparandial nausea-vomiting, and weight loss. paraclinic evaluation revealed hypoalbuminemia and hypochromic microcytic anemia. gastroscopy and barium meal study showed diffuse polypoid, nodular lesions that affected the entire stomach, invaginating into the duodenum, leading to partial duodenal obstruction. the histologic, radiologic and endoscopic findings fulfilled the diagnosis of ménétrier's disease. to the best of our knowledge, gastroduodenal intussusception by ménétrier's disease has been rarely described in the literature. normal 0 false false false en-us x-none fa

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عنوان ژورنال:
middle east journal of digestive diseases

جلد ۵، شماره ۱، صفحات ۵۲-۰

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