Published online Jun 7, 2013. doi: 10.3748/wjg.v19.i21.3358
Revised: March 1, 2013
Accepted: March 15, 2013
Published online: June 7, 2013
Processing time: 139 Days and 19.3 Hours
Solid pseudopapillary neoplasm (SPN) is a rare and low-grade malignant pancreatic neoplasm composed of poorly cohesive monomorphic neoplastic cells forming solid and pseudopapillary structures with frequent hemorrhagic-cystic degeneration. Intraductal papillary mucinous neoplasm (IPMN) is a pancreatic exocrine tumor composed of intraductal papillary growth of mucin containing neoplastic cells in the main pancreatic duct or its major branches. In the case presented here, a 53-year-old, Japanese man was found to have multiple cystic lesions and dilatation of the main pancreatic duct in the neck of the pancreas. Histological examination revealed a main-duct and branch-duct type IPMN, of the gastric-type, involving the neck of the pancreas, associated with a 0.5 cm SPN in the caudal side of the IPMN. We diagnosed this case as synchronous SPN and IPMN. As far as we know, only one other case of synchronous SPN and IPMN has been reported. Both the present case and the previously reported case showed abnormal nuclear expression of β-catenin in SPN, whereas IPMN showed no abnormal nuclear expression. These results suggest that β-catenin abnormality is not a common pathogenetic factor of synchronous SPN and IPMN.
Core tip: We report the second case of synchronous solid pseudopapillary neoplasm (SPN) and intraductal papillary mucinous neoplasm (IPMN) of the pancreas in a 53-year-old Japanese man. IPMN was classified as a “combined” type due to the involvement of both the main and branch ducts, and it showed a gastric subtype with low-grade dysplasia. Adjacent to the caudal side of IPMN, a 0.5-cm solid SPN was present. The SPN showed abnormal nuclear expression of β-catenin in SPN, whereas IPMN showed no abnormal nuclear expression. This result suggested that β-catenin abnormality is not a common pathogenetic factor of synchronous SPN or IPMN.