Publication:
Granulomatosis with polyangiitis presenting as pancreatic pseudotumor and peripancreatic lymphadenitis: diagnostic challenges and review of 55 cases

dc.contributor.coauthorBeniada, Camille
dc.contributor.coauthorCoattrenec, Yann
dc.contributor.coauthorMack, Sahar
dc.contributor.coauthorRicoeur, Alexis
dc.contributor.coauthorPuppa, Giacomo
dc.contributor.coauthorSeebach, Jorg D.
dc.contributor.departmentSchool of Medicine
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.kuauthorFaculty Member, Adsay, Nazmi Volkan
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2025-09-10T04:56:42Z
dc.date.available2025-09-09
dc.date.issued2025
dc.description.abstractObjective: Rare disease Background: The spectrum of anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV) encompasses granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). These pathologies predominantly affect small to medium-sized vessels, with frequent involvement of the ear, nose, and throat (ENT) sphere, lungs, and kidneys. Pancreatic involvement, an exceedingly rare manifestation of AAV, manifests as pancreatitis, a pancreatic mass, or a cystic lesion. This study reports a new case of pancreatic GPA and reviews the literature to characterize its clinical, radiological, and histological features. Case Report: A 54-year-old woman with severe epigastric pain, vomiting, and weight loss presented with a pancreatic mass and peripancreatic lymphadenitis on imaging studies, raising high suspicion for cancer. Repeated endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) biopsies were inconclusive. Distal pancreatectomy with splenectomy was performed. Histopathology demonstrated granulomatous inflammation with necrosis and vasculitis, and anti-PR3 ANCA testing was positive. A diagnosis of GPA was made and treatment with corticosteroids and rituximab resulted in clinical remission. We identified 54 additional cases of pancreatic AAV in the literature and analyzed their clinical features. Conclusions: In cases of unexplained pancreatitis or pancreatic masses/pseudocysts, AAV should be considered. A targeted evaluation-including ANCA testing, imaging, biopsies, and a systematic search for ENT, lung, kidney, and skin manifestations-is essential to identify key clinical, serological, and radiological clues of pancreatic AAV. We propose to classify this as type 4 autoimmune pancreatitis. A corticosteroid-based regimen, with or without additional immunosuppressants, offers effective disease control, making pancreatic surgery unnecessary.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessGold OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.description.volume26
dc.identifier.doi10.12659/AJCR.945741
dc.identifier.eissn1941-5923
dc.identifier.embargoNo
dc.identifier.filenameinventorynoIR06400
dc.identifier.quartileQ3
dc.identifier.scopus2-s2.0-105007889744
dc.identifier.urihttps://doi.org/10.12659/AJCR.945741
dc.identifier.urihttps://hdl.handle.net/20.500.14288/30188
dc.identifier.wos001500747700001
dc.keywordsAutoimmunity
dc.keywordsGranulomatosis with polyangiitis
dc.keywordsPancreatitis
dc.keywordsVasculitis
dc.keywordsPancreatectomy
dc.language.isoeng
dc.publisherInt Scientific Information, Inc
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofAmerican Journal of Case Reports
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectMedicine
dc.titleGranulomatosis with polyangiitis presenting as pancreatic pseudotumor and peripancreatic lymphadenitis: diagnostic challenges and review of 55 cases
dc.typeReview
dspace.entity.typePublication
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