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Exploring the spectrum of incidental gastric polyps in autoimmune gastritis

  • Sara Massironi
    Correspondence
    Corresponding author.
    Affiliations
    Division of Gastroenterology and Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, ASST Monza, Via G.B. Pergolesi 33, Monza e Della Brianza (MB), Monza, Italy

    Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy
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  • Alessandra Elvevi
    Affiliations
    Division of Gastroenterology and Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, ASST Monza, Via G.B. Pergolesi 33, Monza e Della Brianza (MB), Monza, Italy
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  • Camilla Gallo
    Affiliations
    Division of Gastroenterology and Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, ASST Monza, Via G.B. Pergolesi 33, Monza e Della Brianza (MB), Monza, Italy
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  • Alice Laffusa
    Affiliations
    Division of Gastroenterology and Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, ASST Monza, Via G.B. Pergolesi 33, Monza e Della Brianza (MB), Monza, Italy
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  • Anna Tortorella
    Affiliations
    Division of Gastroenterology and Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, ASST Monza, Via G.B. Pergolesi 33, Monza e Della Brianza (MB), Monza, Italy
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  • Pietro Invernizzi
    Affiliations
    Division of Gastroenterology and Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), San Gerardo Hospital, ASST Monza, Via G.B. Pergolesi 33, Monza e Della Brianza (MB), Monza, Italy
    Search for articles by this author
Published:February 27, 2023DOI:https://doi.org/10.1016/j.dld.2023.02.008

      Abstract

      Background

      Gastric polyps represent an abnormal proliferation of the gastric mucosa. Chronic atrophic autoimmune gastritis (CAAG) targets parietal cells and results in hypo-achlorhydria and hypergastrinemia, which exerts a proliferative effect on the gastric mucosa.

      Aims

      We investigate the incidence of gastric polyps in CAAG patients.

      Methods

      This is a single-center retrospective study examining patients with confirmed CAAG from January 1990 until June 2022. Demographic, clinical, biochemical, and serological data were collected for each included patient. The histopathological characteristics of the detected polyps were recorded.

      Results

      A total of 176 CAAG patients were included. Eighty-nine (50.5%) had 163 incidental polyps. Seventy-six patients (85%) had 130 non-endocrine lesions, among which 118 (90.7%) were inflammatory, 6 (4.6%) adenomatous, and 4 (3%) fundic; 33 patients (37%) had gastric neuroendocrine neoplasms (gNENs), and 21 (23.6%) both; one had MALToma and one gastric adenocarcinoma. Higher circulating levels of gastrin and chromogranin A were observed among patients with polyps (median 668 vs 893 pg/ml p = 0.0237, 146 vs 207 ng/ml p = 0.0027, respectively).

      Conclusion

      CAAG implies a high incidence of gNENs and exocrine lesions. Gastrin plays a possible trophic role on the mucosa. Further evidence is needed to validate its predictive role for increased polyp risk in CAAG.

      Keywords

      Abbreviations:

      GPs (gastric polyps), gNENs (gastric neuroendocrine neoplasms), EGD (esophagogastroduodenoscopy), H. Pylori (Helicobacter pylori), PPIs (proton pump inhibitors), CAAG (chronic autoimmune atrophic gastritis), APCA (anti-parietal cell antibodies), IF (intrinsic factor), PG-I (pepsinogen I), BMI (body mass index), PGS (polyglandular syndrome), EMR (endoscopic mucosal resection), EUS (endoscopic ultrasonography), ESD (endoscopic submucosal dissection), OLGA (Operative Link on Gastritis Assessment), OLGIM (Operative Link on Gastric Intestinal Metaplasia), CgA (chromogranin A), SYN (synaptophysin), EDTA (ethylenediaminetetraacetic acid), MCV (mean corpuscular volume), LDH (lactate dehydrogenase), RIA (radiommunoassay), PBC (primary biliary cholangitis), AIH (autoimmune hepatitis), SLE (Systemic Lupus Erythematosus)
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