ArticleWorld journal of clinical cases2020
Localized primary gastric amyloidosis: Three case reports.
Article in World journal of clinical cases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 11 citations in OpenAlex.
- A Case of Localized Gastric Amyloidosis With Improvement on Endoscopy After Eradication of Helicobacter pylori.The Korean journal of helicobacter and upper gastrointestinal research · 2026Article
- Localized light chain amyloidosis of the stomach that regressed after eradication of Helicobacter pylori over 15 years of follow-up: a case report and new hypothesis.Clinical journal of gastroenterology · 2025Article
- Primary Amyloidosis Unmasked by Gastric Biopsy: A Case Report.Clinical medicine insights. Case reports · 2025Article
- Alpha-Fetoprotein-Producing Hepatoid Adenocarcinoma of the Stomach.Journal of medical cases · 2024Article
- Gastrointestinal amyloidosis in a 50-year-old patient with miliary tuberculosis: A case report.Clinical case reports · 2024Article
- Article
- Gastroduodenal amyloidosis: a case report and review of literature.Journal of surgical case reports · 2021Article
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundLocalized primary gastric amyloidosis is a rare disorder characterized by the extracellular deposition of insoluble fibrillary protein in the stomach and can mimic various diseases on endoscopic examination, including gastrointestinal stromal tumors, gastric cancer and ulcers. CASE SUMMARIES: Here, we report a series of three cases of localized gastric amyloidosis mimicking gastric mucosa-associated lymphoid tissue (MALT) lymphoma on endoscopic examination that were evaluated over the past ten years in our hospital. The different detection times of this rare disease resulted in three completely different outcomes, indicating the strong importance of early detection, diagnosis and treatment. The difficulties encountered in making an accurate diagnosis and differential diagnosis are highlighted, and this report provides clinical experience for the diagnosis of localized primary gastric amyloidosis.
conclusionLocalized gastric amyloidosis is a rare metabolic disease that resembles MALT lymphoma. Early detection, diagnosis and treatment of localized gastric amyloidosis result in an excellent prognosis.
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