31 May 2025
: Case report
Granulomatosis with Polyangiitis Presenting as Pancreatic Pseudotumor and Peripancreatic Lymphadenitis: Diagnostic Challenges and Review of 55 Cases
Mistake in diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)
Camille Beniada ABCEF 1, Yann Coattrenec AE 1, Sahar MackDOI: 10.12659/AJCR.945741
Am J Case Rep 2025; 26:e945741
Figure 2 (A) Macroscopy of the pancreatic resection showing a 6.5×4.2×3.5 cm mass that was encapsulated, firm, heterogeneous, whitish-to-yellowish, with intermingled adipose tissue, no calcifications, no dilatation of the pancreatic ducts, and no associated cystic lesions; (B–D) histology: (B) low magnification of the granulomatous fibro-inflammatory and necrotic process; (C) higher magnification showing several multi-nucleated giant cells; (D) higher magnification of the blood vessel contained in the box of Figure 2B showing infiltration of the vessel walls by lymphoplasmacytic cells; (E) necrotizing vasculitis with vessel wall infiltration (higher magnification 12×), arrow – inflammatory lymphocytic infiltrate; star – necrosis.






