Primary Hepatic Neuroendocrine Tumor: A Case Report and Literature Review
View abstract on PubMed
Summary
This summary is machine-generated.Primary hepatic neuroendocrine tumors (PHNETs) are rare malignant tumors. This case highlights successful surgical resection of a previously unresectable PHNET, offering curative potential.
Area Of Science
- Hepatobiliary surgery
- Surgical oncology
- Gastroenterology
Background
- Primary hepatic neuroendocrine tumors (PHNETs) are exceptionally rare, comprising only 0.3% of all neuroendocrine tumors.
- Diagnosis often occurs at advanced stages, complicating surgical resection.
- PHNETs necessitate a high index of suspicion, especially after ruling out primary extrahepatic lesions.

