alexa Menetrier Disease in a Five Year Old Girl - A Case Repo
ISSN: 2161-069X

Journal of Gastrointestinal & Digestive System
Open Access

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Case Report

Menetrier Disease in a Five Year Old Girl - A Case Report and Review of Literature

Virtut Velmishi1*, Besnik Elezi2and Gentiana Cekodhima3

1Service of Pediatric nr 2, “Mother Teresa Hospital”-Tirana, Albania

2Service of Gastroenterology, Regional hospital of Gjilan –Kosovo, Albania

3Service of Histopathology, “Mother Teresa Hospital”-Tirana, Albania

Corresponding Author:
Virtut Velmishi
Service of Pediatric nr 2; “Mother Teresa Hospital”-Tirana, Albania
Tel: 00355672057335
E-mail: [email protected] com

Received Date: January 23, 2016 Accepted Date: February 29, 2016 Published Date: March 04, 2016

Citation:Velmishi V, Elezi B, Cekodhima G (2016) Menetrier Disease in a Five Year Old Girl - A Case Report and Review of Literature. J Gastrointest Dig Syst 6:395. doi:10.4172/2161-069X.1000395

Copyright: © 2016 Velmishi V, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Introduction: Menetrier`s disease is one of the rarest protein losing gastropathies in childhood characterized by hypertrophy of gastric folds. Children with Menetrier disease tend to follow a self-limited course with symptoms typically completely resolving within 2 to 10 weeks.

Case report: A five year old girl presented fever for two days, abdominal pain and vomiting. After two other days she presented periorbital swelling and skin rash. Laboratory findings on admission showed hypoalbuminemia and eosinophilia. Screening for Helicobacter pylori and cytomegalovirus resulted negative. Abdominal ultrasonography showed moderate ascitis and in chest X ray revealed effusion in both lungs. Gastroscopy showed severe erosions in fundus and in upper part of stomach body. The lower part of stomach and antrum was normal. Histopathology showed data compatible with Menetrier disease. She was treated with several albumin infusions and diuretics and her symptoms improved after 4 weeks of treatment.

Conclusion: This is the first case of pediatric MD in our experience. Endoscopic images and histological data are very important to support

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