Co-Infection with Cytomegalovirus and Helicobacter pylori in a Child with Ménétrier’s Disease
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초록
Ménétrier’s disease is a rare protein-losing gastropathy characterized by hypertrophic gastric fold, foveolar hyperplasia, and hypoproteinemia with resulting peripheral edema. It is clinically evident as nonspecific gastrointestinal symptoms, including abdominal discomfort, nausea and vomiting, abdominal pain, weight loss, diarrhea, and edema. Pediatric Ménétrier’s disease usually has an insidious onset and progressive, chronic clinical course and it spontaneously resolves in weeks or months. The pathogenesis of Ménétrier’s disease is not clearly understood. Ménétrier’s disease is thought to be associated with some gastric infections. But the cause of Ménétrier’s disease is unknown, an association with cytomegalovirus (CMV) and Helicobacter pylori has been suggested. In Korea, We present the first a case of pediatric Ménétrier’s disease with positive evidence of CMV and H. pylori. (Pediatr Gastroenterol Hepatol Nutr 2013; 16: 123∼126)
Abstract
Ménétrier’s disease is a rare protein-losing gastropathy characterized by hypertrophic gastric fold, foveolar hyperplasia, and hypoproteinemia with resulting peripheral edema. It is clinically evident as nonspecific gastrointestinal symptoms, including abdominal discomfort, nausea and vomiting, abdominal pain, weight loss, diarrhea, and edema. Pediatric Ménétrier’s disease usually has an insidious onset and progressive, chronic clinical course and it spontaneously resolves in weeks or months. The pathogenesis of Ménétrier’s disease is not clearly understood. Ménétrier’s disease is thought to be associated with some gastric infections. But the cause of Ménétrier’s disease is unknown, an association with cytomegalovirus (CMV) and Helicobacter pylori has been suggested. In Korea, We present the first a case of pediatric Ménétrier’s disease with positive evidence of CMV and H. pylori. (Pediatr Gastroenterol Hepatol Nutr 2013; 16: 123∼126)
참고문헌 (20)
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