Copyright: ©Author(s) 2026.
World J Clin Oncol. Mar 24, 2026; 17(3): 114990
Published online Mar 24, 2026. doi: 10.5306/wjco.v17.i3.114990
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 positivity | Variable 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 radiologically | Occult 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 |
- Citation: Alghamdi TH. When to operate pancreatic intraductal papillary mucinous neoplasm: Literature review. World J Clin Oncol 2026; 17(3): 114990
- URL: https://www.wjgnet.com/2218-4333/full/v17/i3/114990.htm
- DOI: https://dx.doi.org/10.5306/wjco.v17.i3.114990