[PDF][PDF] Two cases of primary hepatic neuroendocrine tumors and a review of the current literature

MR DeLuzio, AL Barbieri, G Israel, S Emre - Annals of Hepatology, 2017 - medigraphic.com
ABSTRACT Neuroendocrine tumors comprise approximately 1-2% of all gastrointestinal
tumors, and while the liver is the most common site for metastasis of these tumors, primary …

[HTML][HTML] Clinical characteristics and outcome of primary hepatic neuroendocrine tumors after comprehensive therapy

HH Wang, ZC Liu, G Zhang, LH Li, L Li… - World Journal of …, 2020 - ncbi.nlm.nih.gov
BACKGROUND Primary hepatic neuroendocrine tumors (PHNETs), a group of
neuroendocrine neoplasms, are extremely rare. There are only few case reports about …

The outcome of primary hepatic neuroendocrine tumors: a single-center experience

D Shah, A Mandot, C Cerejo, D Amarapurkar… - Journal of Clinical and …, 2019 - Elsevier
Background Primary hepatic neuroendocrine tumor is an extremely rare entity. Only case
reports are available in the literature. The aim of the study was to analyze the symptoms …

Primary hepatic neuroendocrine neoplasm presenting as a massive cystic liver tumor mimicking mucinous cystic neoplasm of the liver: A case report and literature …

T Noro, T Tatsuoka, M Takada… - Oncology …, 2023 - spandidos-publications.com
Neuroendocrine neoplasms (NENs) preferentially arise in the bronchopulmonary tree or the
gastrointestinal tract. Notably, primary hepatic NENs are extremely rare. The present study …

[HTML][HTML] Primary hepatic neuroendocrine tumours—Case series of a rare malignancy

N Chen, K Slater - International Journal of Surgery Case Reports, 2019 - Elsevier
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 …

Primary hepatic origin of a neuroendocrine tumor: A rare case report

L Bouzayan, A Madani, S Malki, W Abbou… - Annals of Medicine …, 2022 - journals.lww.com
Primary hepatic origin of a neuroendocrine tumor: A rare cas... : Annals of Medicine and
Surgery Primary hepatic origin of a neuroendocrine tumor: A rare case report : Annals of …

[PDF][PDF] Primary hepatic neuroendocrine tumor with ectopic adrenocorticotropic hormone production

R Waghela, U Ansari, A Shetty, D Victor, S Kodali - Cureus, 2022 - cureus.com
This report describes the case of a 63-year-old female with a metastatic neuroendocrine
tumor (NET). Imaging studies revealed a primary hepatic NET (PHNET) originating in the …

A case of primary hepatic mixed neuroendocrine-non-neuroendocrine tumor (MiNEN) associated with gallbladder carcinosarcoma

R Kaneko, Y Kimura, H Sakata, T Ikehara… - Clinical Journal of …, 2020 - Springer
A woman in her seventies visited our hospital because of abdominal pain. Multiple hepatic
tumors were detected and a liver biopsy revealed mixed neuroendocrine-non …

原发性肝脏神经内分泌肿瘤13 例临床病理分析

王锋, 刘秀峰, 秦叔逵, 华海清, 李桂梅, 袁梅 - 中华肿瘤防治杂志, 2016 - cqvip.com
目的原发性肝脏神经内分泌肿瘤(primary hepatic neuroendocrine neoplasm, PHNEN)
是罕见肿瘤. 本研究通过对13 例PHNEN 的诊治过程进行分析总结, 并结合相关文献深入探讨 …

[HTML][HTML] Complete Response After Pre-Operative Transcatheter Arterial Chemoembolization for Unresectable Primary Hepatic Neuroendocrine Tumour: A Case …

X Zhang, H Yang, Y Xin, Y Yang, H Lu, X Zhou - Frontiers in Oncology, 2022 - frontiersin.org
Background Primary hepatic neuroendocrine tumours (PHNET) are extremely rare.
Currently, no evidence-based guidelines are available for PHNET treatment, especially for …