Case Report
Copyright ©The Author(s) 2025.
World J Clin Oncol. Mar 24, 2025; 16(3): 101236
Published online Mar 24, 2025. doi: 10.5306/wjco.v16.i3.101236
Table 2 Differential diagnosis of pancreatic neuroendocrine neoplasms with hepatocellular carcinoma and cholangiocarcinoma

PHNENs
HCC
CCC
SourceNeuroendocrine cellsLiver cellsBile duct cells
Incidence rate (of all hepatic cancers)0.28%-0.46%80%15%
Risk factorsUn clearViral hepatitis, alcoholic liver disease, non-alcoholic fatty liver disease, aflatoxinCholangitis, bile duct stones, bile duct cysts, hepatic schistosome infection
Clinical manifestationsNo manifestations in the early stage. Abdominal pain, jaundice and an epigastric mass in the late stage. Functional PHNENs may be associated with carcinoid syndromeNo manifestations in the early stage. The first symptom is abdominal pain, followed by an epigastric mass, fatigue, lethargy and abdominal distensionNo manifestations in the early stage. Abdominal discomfort, abdominal pain, fatigue, nausea, an epigastric mass, jaundice and fever in the late stage
Imaging manifestationsSingle or multiple low-density nodules or inhomogeneous masses in the liver, often with cystic degeneration or liquefied necrosis‘Fast-in-fast-out’ enhancement pattern on CT/MRIBile duct dilatation, thickening of the bile duct wall or periductal infiltration on CT/MRI, and a slowly progressive enhancement on enhanced imaging
Serum tumor markersNo specific tumor markers. Serotonin, insulin and gastrin elevated in the functional PHNENsAFP, PIVKA II, AFP-L3, microRNA elevatedNo specific tumor markers. CA19-9, CA125 and CEA elevated
Immunohistochemical markersCgA, Syn, NSE, CD56HepPar1, CD34, pCEA, COX-2, arginase-1MUC-1, CK19, AQP-1
TreatmentPreferred surgeryPreferred surgeryPreferred surgery