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Quartey B. Primary Hepatic Neuroendocrine Tumor: What Do We Know Now?. World J Oncol. 2011;2(5):209-216doi: 10.4021/wjon341w.
Quartey, B. (2011). Primary Hepatic Neuroendocrine Tumor: What Do We Know Now?. World journal of oncology, 2(5), 209-216. https://doi.org/10.4021/wjon341w
Quartey, Benjamin. "Primary Hepatic Neuroendocrine Tumor: What Do We Know Now?." World journal of oncology vol. 2,5 (2011): 209-216. doi: https://doi.org/10.4021/wjon341w
Quartey B. Primary Hepatic Neuroendocrine Tumor: What Do We Know Now?. World J Oncol. 2011 Oct;2(5):209-216. doi: 10.4021/wjon341w. Epub 2011 Oct 28. PMID: 29147250; PMCID: PMC5649681.
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World J Oncol. 2011 Oct;2(5):209-216. doi: 10.4021/wjon341w. Epub 2011 Oct 28.

Primary Hepatic Neuroendocrine Tumor: What Do We Know Now?.

World journal of oncology

Benjamin Quartey

Affiliations

  1. National Capital Consortium, National Naval Medical Center, Department of Surgery, 8901 Wisconsin Ave, Bethesda, MD 20889, USA.

PMID: 29147250 PMCID: PMC5649681 DOI: 10.4021/wjon341w

Abstract

Primary hepatic neuroendocrine tumors (PHNETs) are rear neoplasm. Diagnosis is an evolution, and requires a systematic clinical exclusion with histological confirmation. Treatment is surgical with excellent prognosis, and a long-term follow-up is required due to high tumor recurring rate. Knowledge from this species of tumor remains limited due to paucity of cases. This article elaborates the key features, diagnosis algorithm, current management, other treatment options and extensive review of literature on this rear tumor.

Keywords: Carcinoid; Liver; Neuroendocrine tumor; Primary hepatic tumor

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