[A young man with acute, generalised oedema]

Tidsskr Nor Laegeforen. 2010 Aug 26;130(16):1627-9. doi: 10.4045/tidsskr.09.0771.
[Article in Norwegian]

Abstract

Background: Ménétrier disease is an uncommon, idiopathic disease characterized by development of chronic protein loss from marked gastric foveolar hyperplasia. A literature search identified several reports of self-limiting, cytomegalovirus-associated Ménétrier disease in children. Some cases have also been reported in adults.

Case report: A formerly healthy man was admitted to hospital with a serum albumin level of 11 g/l and generalised oedema. Transabdominal ultrasound and endoscopy revealed a folded thickening of the (abdominal) ventricular wall; indications of Ménétrier disease. Histological examination of endoscopic biopsies showed moderate hyperplasia in foveolar epithelium, but also suggested an infectious cause. Intranucleal inclusion bodies, CMV-specific immunology, PCR and special stains all supported cytomegalovirus infection. The patient recovered quickly on antiviral treatment.

Conclusion: Our case demonstrates that cytomegalovirus may cause severe, Ménétrier-like gastritis with protein loss in non-immune-compromised adults.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adult
  • Cytomegalovirus Infections / diagnosis*
  • Cytomegalovirus Infections / drug therapy
  • Diagnosis, Differential
  • Edema / diagnosis*
  • Endosonography
  • Gastric Mucosa / pathology
  • Gastritis / drug therapy
  • Gastritis / virology*
  • Gastritis, Hypertrophic / diagnosis
  • Gastroscopy
  • Humans
  • Male
  • Protein-Losing Enteropathies / diagnosis