Published online Apr 14, 2014. doi: 10.3748/wjg.v20.i14.4102
Revised: September 14, 2013
Accepted: October 17, 2013
Published online: April 14, 2014
Processing time: 350 Days and 5.7 Hours
Cystic hepatic neoplasms are rare tumors, and are classified into two separate entities: mucinous cystic neoplasms (MCNs) and intraductal papillary mucinous neoplasms of the bile duct (IPMN-B). We report the case of a 56-year-old woman who presented with abdominal pain and jaundice due to the presence of a large hepatic multilocular cystic tumor associated with an intraductal tumor. Partial hepatectomy with resection of extrahepatic bile ducts demonstrated an intrahepatic MCN and an intraductal IPMN-B. This is the first report of the simultaneous occurrence of these two histologically distinct entities in the liver.
Core tip: Cystic hepatic neoplasms are rare tumors, and are classified as mucinous cystic neoplasms (MCN) characterized by intracystic septae, ovarian-like stroma, and no communication with bile ducts; and intraductal papillary mucinous neoplasms of the bile duct (IPMN-B) characterized by intraductal growth, dilated bile ducts, and papillary projections. We report a 56-year-old woman diagnosed with a large multilocular cystic tumor in the liver and in dilated extrahepatic bile ducts that were two histologically distinct cystic tumors. This is the first report of the simultaneous occurrence of MCN and IPMN-B. We present diagnostic considerations, therapeutic approaches, and the prognosis of cystic tumors of the liver.