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Gastric mucosal hypertrophy

MedGen UID:
4844
Concept ID:
C0017155
Disease or Syndrome
Synonyms: GASTRITIS, FAMILIAL GIANT HYPERTROPHIC; Gastritis, Hypertrophic; Gastroenteropathy, protein losing; Giant hypertrophic gastritis; Giant hypertrophic gastropathy; Giant hypertrophy of the gastric mucosa; Hypertrophic gastropathy; Menetrier disease
SNOMED CT: Hypertrophic gastropathy (413219009); Gastric hyperplasia (60002000); Gastric mucosal hyperplasia (60002000); Giant rugal hypertrophy of stomach (60002000); Hyperplastic gastropathy (60002000); Hyperplastic gastropathy of mucous cell type (60002000); Hypertrophic bulbous gastritis (60002000); Menetrier disease (60002000); Proliferative chronic hypertrophic gastritis (60002000); Polypoid swelling of gastric mucous membrane (60002000); Massive hypertrophic gastritis (60002000); Hypertrophic proliferative gastritis (60002000); Adenopapillomatosis gastrica (60002000); Giant hypertrophic gastritis (60002000); Gastritis hypertrophica gigantica (60002000); Gastritis hypertrophica gigantea (60002000); Hypertrophic gastritis (60002000); Ménétrier's disease (60002000); Gastric mucosal hypertrophy (60002000); Gastritis hypertrophic gigantica (60002000); Giant rugal gastritis (60002000); Chronic hypertrophic gastritis (60002000); Giant rugal hypertrophy (60002000)
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
141047
Concept ID:
C0443147
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.
Unknown inheritance
MedGen UID:
989040
Concept ID:
CN307042
Finding
Source: Orphanet
Hereditary clinical entity whose mode of inheritance is unknown.
Not genetically inherited
MedGen UID:
988794
Concept ID:
CN307044
Finding
Source: Orphanet
clinical entity without genetic inheritance.
 
HPO: HP:0005246
Monarch Initiative: MONDO:0007652
OMIM®: 137280
Orphanet: ORPHA2494

Definition

A type of gastritis characterized by excessive proliferation of the gastric mucosa and diffuse thickening of the gastric mucosal folds. [from HPO]

Clinical features

From HPO
Vascular dilatation
MedGen UID:
8076
Concept ID:
C0002940
Pathologic Function
Abnormal outpouching or sac-like dilatation in the wall of an atery, vein or the heart.
Gastric mucosal hypertrophy
MedGen UID:
4844
Concept ID:
C0017155
Disease or Syndrome
A type of gastritis characterized by excessive proliferation of the gastric mucosa and diffuse thickening of the gastric mucosal folds.
Hypoproteinemia
MedGen UID:
581229
Concept ID:
C0392692
Finding
A decreased concentration of protein in the blood.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVGastric mucosal hypertrophy
Follow this link to review classifications for Gastric mucosal hypertrophy in Orphanet.

Conditions with this feature

Gastric mucosal hypertrophy
MedGen UID:
4844
Concept ID:
C0017155
Disease or Syndrome
A type of gastritis characterized by excessive proliferation of the gastric mucosa and diffuse thickening of the gastric mucosal folds.

Professional guidelines

PubMed

Katzka DA, Loftus EV Jr, Camilleri M
Clin Pharmacol Ther 2012 Sep;92(3):306-20. Epub 2012 Jul 25 doi: 10.1038/clpt.2012.77. PMID: 22828717
Kyrlagkitsis I, Karamanolis DG
Hepatogastroenterology 2003 Mar-Apr;50(50):592-600. PMID: 12749280
Okanobu H, Hata J, Haruma K, Hara M, Nakamura K, Tanaka S, Chayama K
Radiology 2003 Mar;226(3):686-90. Epub 2003 Jan 24 doi: 10.1148/radiol.2263012080. PMID: 12601220

Recent clinical studies

Diagnosis

Malik D, Elumalai R, Verma R, Belho ES, Seniaray N, Mahajan H
Clin Nucl Med 2020 Jan;45(1):74-75. doi: 10.1097/RLU.0000000000002802. PMID: 31693612
Chebli JMF, Chebli LA, Ribeiro TCDR, Gaburri PD
Rev Assoc Med Bras (1992) 2017 Mar;63(3):215-218. doi: 10.1590/1806-9282.63.03.215. PMID: 28489125
Dong A, Zhang L, He T, Zuo C
Clin Nucl Med 2016 Jul;41(7):e348-50. doi: 10.1097/RLU.0000000000001133. PMID: 26825202
Callahan MJ, McCauley RG, Patel H, Hijazi ZM
Pediatr Radiol 1999 Oct;29(10):748-51. doi: 10.1007/s002470050688. PMID: 10525782
SUSSMAN HM, WEINGARTEN B, MOSSBERG SM
Am J Dig Dis 1965 Aug;10:710-8. doi: 10.1007/BF02236071. PMID: 14316759

Therapy

Callahan MJ, McCauley RG, Patel H, Hijazi ZM
Pediatr Radiol 1999 Oct;29(10):748-51. doi: 10.1007/s002470050688. PMID: 10525782

Supplemental Content

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