Gastric dysplastic lesions in Helicobacter pylori-naïve stomach: Foveolar-type adenoma and intestinal-type dysplasia

Pathol Int. 2024 Aug;74(8):423-437. doi: 10.1111/pin.13456. Epub 2024 Jun 5.

Abstract

Reports of Helicobacter pylori (Hp)-naïve gastric neoplasm (HpNGN) cases have been rapidly increasing due to the recent increase in the Hp-naïve population in Japan. Most HpNGNs exhibit the gastric immunophenotype and a low malignant potential regardless of histological type. Especially, foveolar-type gastric adenoma (FGA) and intestinal-type gastric dysplasia (IGD) rarely progress to invasive carcinoma. FGA is a foveolar epithelial neoplasm that occurs in the fundic gland (oxyntic gland) mucosa and is classified as the flat type or raspberry type (FGA-RA). The flat type is a large, whitish flatly elevated lesion while FGA-RA is a small reddish polyp. Genomically, the flat type is characterized by APC and KRAS gene mutations and FGA-RA by a common single nucleotide variant in the KLF4 gene. This KLF4 single-nucleotide variant reportedly induces gastric foveolar epithelial tumorigenesis and activates both cell proliferation and apoptosis, leading to its slow-growing nature. IGD consists of an intestinalized epithelial dysplasia that develops in the pyloric gland mucosa, characterized as a superficial depressed lesion surrounded by raised mucosa showing a gastritis-like appearance. Immunohistochemically, it exhibits an intestinal or gastrointestinal phenotype and, frequently, p53 overexpression. Thus, IGD shows unique characteristics in HpNGNs and a potential multistep tumorigenic process.

Keywords: Helicobacter pylori; KLF4; foveolar‐type gastric adenoma; gastric dysplasia; intestinal‐type gastric dysplasia.

Publication types

  • Review

MeSH terms

  • Adenoma* / microbiology
  • Adenoma* / pathology
  • Gastric Mucosa* / microbiology
  • Gastric Mucosa* / pathology
  • Helicobacter Infections / complications
  • Helicobacter Infections / microbiology
  • Helicobacter Infections / pathology
  • Helicobacter pylori* / isolation & purification
  • Humans
  • Kruppel-Like Factor 4*
  • Mutation
  • Precancerous Conditions / microbiology
  • Precancerous Conditions / pathology
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Stomach / microbiology
  • Stomach / pathology
  • Stomach Neoplasms* / microbiology
  • Stomach Neoplasms* / pathology

Substances

  • Kruppel-Like Factor 4
  • KLF4 protein, human
  • Proto-Oncogene Proteins p21(ras)