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World J Clin Oncol. Mar 24, 2026; 17(3): 114990
Published online Mar 24, 2026. doi: 10.5306/wjco.v17.i3.114990
Table 2 It summarizes the differential diagnosis of intraductal papillary mucinous neoplasms
Intraductal oncocytic papillary neoplasm
Intraductal tubulopapillary neoplasm
Mucinous cystic neoplasm
Pancreatic intraepithelial neoplasia
Simple mucinous cyst
Retention cyst
Variable sizes. Arborizing lined by oncocytic cells. It has a different molecular genetic alteration in one of the following genes, ARHGAP26, ASXL1, EPHA8 and ERBB4. DNAJB1-PRKACA fusions. MUC1 and MUC6 positivityVariable sizes subtype originating from peribiliary cysts. Tributary epithelial cells forming papillary and tubular patterns. High-grade dysplasia solid growth with necrotic foci, little or invisible mucin with intracytoplasmic mucin is present. No mutations in KRAS2 positivity for MUC1+, MUC6+ and negativity for MUC2-Variable sizes. This cyst is lined by epithelial mucinous layer and stroma of ovarian type. No anatomical communication with pancreatic duct or its branches radiologicallyOccult mass. Detected microscopically. Epithelial differentiation towards gastric foveolar epithelium> 1 cm. Flat epithelium (differentiated towards gastric mucinous type). No papillae. Little atypia> 1 cm. Simple flat epithelial lining. No papillae. Little atypia


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