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Unusual case of adult familial Menetrier disease in siblings
- Source :
- BMJ Case Rep
- Publication Year :
- 2019
- Publisher :
- BMJ, 2019.
-
Abstract
- Menetrier disease is a rare disease characterised by hyperplasia of the gastric epithelium and large gastric folds. We present a case of a 58-year-old woman who was referred with iron deficiency anaemia, with a family history of a sibling who had undergone gastrectomy for presumed gastric malignancy. Endoscopy showed prominent gastric mucosal folds and biopsies showed hyperplastic gastric mucosa, with prominent foveolar hyperplasia suggestive of Menetrier disease. Further information about her brother’s diagnosis was sought, and it was found that his pathology after gastrectomy showed diffuse glandular hyperplasia also in keeping with Menetrier disease. Adult familial Menetrier disease has so far been a rarity in the literature—review elicits five previous cases of this presentation in siblings.
- Subjects :
- Male
0301 basic medicine
medicine.medical_specialty
medicine.medical_treatment
030105 genetics & heredity
Gastroenterology
Endoscopy, Gastrointestinal
03 medical and health sciences
Rare Diseases
0302 clinical medicine
Rare Disease
Internal medicine
Gastric mucosa
Humans
Medicine
Sibling
Family history
Gastritis, Hypertrophic
Hyperplasia
medicine.diagnostic_test
business.industry
Siblings
General Medicine
Middle Aged
medicine.disease
Endoscopy
Foveolar cell
medicine.anatomical_structure
Gastric Mucosa
Female
Gastrectomy
business
030217 neurology & neurosurgery
Rare disease
Subjects
Details
- ISSN :
- 1757790X
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- BMJ Case Reports
- Accession number :
- edsair.doi.dedup.....fd240680841d456316ac8f920a297824