Ménétrier's disease in pediatric patients secondary to cytomegalovirus infection: Presentation of two clinical cases in a high complexity center

Ménétrier's disease is a protein losing gastroenteropathy. Defined as a rare entity with an unknown cause, most of the reported cases have been associated with viral infections. In pediatric patients, it is characterized by an acute onset with a benign and self-limiting course. It is characteri...

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Veröffentlicht in:Archivos argentinos de pediatría 2019-04, Vol.117 (2), p.e158-e162
Hauptverfasser: Tagliaferro, Gustavo, Llera, Julián, Orsi, Marina
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Llera, Julián
Orsi, Marina
description Ménétrier's disease is a protein losing gastroenteropathy. Defined as a rare entity with an unknown cause, most of the reported cases have been associated with viral infections. In pediatric patients, it is characterized by an acute onset with a benign and self-limiting course. It is characterized by thickened gastric folds that generally involve the body and the gastric fundus, associated with hypoalbuminemia due to the loss of serum protein through the mucosa. The following are two clinical cases of infant Ménétrier syndrome associated with cytomegalovirus infection.
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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Child, Preschool
Cytomegalovirus Infections - complications
Gastric Mucosa - pathology
Gastritis, Hypertrophic - diagnosis
Gastritis, Hypertrophic - microbiology
Humans
Infant
Male
title Ménétrier's disease in pediatric patients secondary to cytomegalovirus infection: Presentation of two clinical cases in a high complexity center
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