An Association of Autoimmune Pancreatitis and Allergic Disorders: A Possible Overlap Syndrome
DOI :
https://doi.org/10.71599/bhr.v7i1.170Mots-clés :
Autoimmune pancreatitis, Eosinophilic pancreatitis, IgG4-related disease, Allergic disorders, Eosinophilia, SteroidRésumé
Autoimmune pancreatitis (AIP) is a rare and distinct form of chronic pancreatitis, characterized by unique clinical, radiological, and histopathological features. Its prevalence is 2–4 per 100,000, with up to 40% of patients showing eosinophilia or other allergic manifestations (1). The association between AIP and allergic disorders accompanied by pancreatic eosinophilia is rare and poorly characterized, with few documented cases in the literature, making its recognition particularly challenging. We describe a case of AIP in a 65-year-old woman with asthma, diabetes, and chronic renal insufficiency. The patient presented with symptoms mimicking pancreatic malignancy, but further investigations revealed AIP with significant peripheral and tissue eosinophilia. She demonstrated marked clinical and radiological improvement following corticosteroid therapy, with rapid resolution of symptoms and normalization of eosinophil counts within 10 days, and remained in remission during a 6-month follow-up. This case highlights the rare overlap between AIP and eosinophilic disorders, suggesting a possible link with allergic conditions that deserves further study
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(c) Tous droits réservés Dhouha Bacha, Dorsaf Beltaifa, Nour Boudriga, Monia Attia, Leila Ben Farhat, Sana Ben Slama, Ahlem Lahmar 2026

Ce travail est disponible sous licence Creative Commons Attribution - Pas d'Utilisation Commerciale - Pas de Modification 4.0 International.