ArticleEuropean journal of case reports in internal medicine2025
Autoimmune Polyglandular Syndrome Type 3b: A Key to Diagnosing Autoimmune Gastritis and Asymptomatic Primary Biliary Cholangitis.
Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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2 citing papers in PubMed.
- Editorial: Advancing immune research in chronic liver diseases through new approach methodologies.Frontiers in immunology · 2026Article
- Immunological and clinical overlap between autoimmune gastritis and autoimmune liver diseases: a prospective cohort study.Frontiers in immunology · 2025Article
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3 authors.
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Abstract
Background: Autoimmune polyglandular syndrome type 3 (APS-3) encompasses autoimmune thyroid disease and other autoimmune disorders. APS-3 is further categorized into four subtypes, with APS-3B involving gastrointestinal autoimmune diseases. In this case, we diagnosed autoimmune gastritis, a condition challenging to identify based on endoscopic findings alone, and asymptomatic primary biliary cholangitis (PBC) through the recognition of APS-3B. Case report: An 84-year-old female patient presented with forgetfulness and a history of Hashimoto's disease. Although endoscopy revealed pan-atrophic gastritis, autoimmune gastritis was suspected rather than Conclusion: Recognition of APS-3 offers a valuable framework for the differential diagnosis of autoimmune diseases. LEARNING POINTS: Autoimmune thyroid disease in a patient should raise suspicion for autoimmune polyglandular syndrome type 3 (APS-3) and other potential autoimmune conditions.If APS-3 is diagnosed, further classification is recommended, along with a thorough search for additional autoimmune diseases.APS-3 serves as a framework for the differential diagnosis of autoimmune diseases.
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