Primary hepatic neuroendocrine tumor with repeated diarrhea and flushing face: A case report and literature review
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View abstract on PubMed
Summary
This summary is machine-generated.Primary hepatic neuroendocrine tumors (PHNET) are rare liver tumors. This case highlights a PHNET patient with diarrhea and flushing, effectively treated with transcatheter arterial chemoembolization (TACE).
Area Of Science
- Hepatology
- Oncology
- Gastroenterology
Background
- Primary hepatic neuroendocrine tumors (PHNET) are rare, accounting for only 0.3% of all neuroendocrine tumors.
- Abdominal pain is the most common symptom, while diarrhea and flushing are less frequent.
- This report focuses on a rare case of PHNET presenting with prominent gastrointestinal and dermatological symptoms.
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