Middle East Journal of Digestive Diseases. 2013; 5 (1): 52-55
em Inglês
| IMEMR
| ID: emr-130196
ABSTRACT
Menetrier'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 Menetrier's disease. To the best of our knowledge, gastroduodenal intussusception by Menetrier's disease has been rarely described in the literature
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Gastropatias
/
Bário
/
Gastroscopia
/
Duodenopatias
/
Intussuscepção
Tipo de estudo:
Relato de Casos
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
Middle East J. Dig. Dis.
Ano de publicação:
2013
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