Introduction Primary hepatic neuroendocrine tumours (PHNET) were first described by
Edmondson et al. in 1958 and are rare, accounting for only 0.3% of all neuroendocrine …

Introduction Primary hepatic neuroendocrine tumors (PHNETs) are extremely rare, having
less than 200 cases reported in the literature. Presentation of case A 51-year-old woman …

Primary hepatic neuroendocrine tumors (PHNETs) are extremely rare and account for about
0.3% of all neuroendocrine tumor cases. Resection is usually difficult because they are …

Primary hepatic neuroendocrine tumours (PHNETs) were described by Edmondson in 1958.
1 They are rare primary hepatic tumours that constitute 0.3% of all neuroendocrine tumours …

Primary hepatic neuroendocrine tumors (PHNETs) are extremely rare and asymptomatic. It
is radiologically difficult to distinguish from other liver tumors, such as hepatocellular …

Introduction Primary hepatic neuroendocrine tumours (PHNETs) are a rare form of hepatic
neoplasms, and it is difficult to differentiate them from common hepatic malignancies in …

Interventions: Biochemical examination and imaging examination were performed prior to
operation. Liver tumors were removed by ultrasound scalpel under laparoscopy. Pathology …

Primary hepatic neuroendocrine tumor — 18F-fluorodeoxyglucose positron emission
tomography/computed tomography findings: A case report - PMC Back to Top Skip to main …

Background & Aims Primary hepatic neuroendocrine tumors (PHNETs) are rare malignant
liver tumors that present diagnostic challenges owing to their rarity and absence of specific …

Background: A primary hepatic neuroendocrine tumour (PHNET) is a very rare disease. The
liver represents the preferential site for neuroendocrine tumors' metastases. Case …