[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 …

Diagnostic imaging of primary hepatic neuroendocrine tumors: a case and discussion of the literature

T Kellock, B Tuong, AC Harris… - Case Reports in …, 2014 - Wiley Online Library
Neuroendocrine tumors (NETs) are derived from neuroendocrine cells that are capable of
producing functional peptide hormones. These tumors occur most frequently in the GI tract …

[HTML][HTML] Childhood neuroendocrine tumors of the digestive system: A single center experience

İ Kartal - Medicine, 2022 - journals.lww.com
The prevalence and incidence of neuroendocrine tumors (NETs) are increasing in the
pediatric population. This increase can be associated with improved diagnostics and …

Primary hepatic neuroendocrine neoplasm: long-time surgical outcome and prognosis

C Shi, Q Zhao, B Dai, F Xie, J Yang - Medicine, 2018 - journals.lww.com
Primary hepatic neuroendocrine neoplasm: Long-time surgical... : Medicine Primary hepatic
neuroendocrine neoplasm: Long-time surgical outcome and prognosis : Medicine Log in or …

Development of a nomogram model to predict survival outcomes in patients with primary hepatic neuroendocrine tumors based on SEER database

Z Zhang, X Zhao, Z Li, Y Wu, Y Liu, Z Li, G Li - BMC cancer, 2021 - Springer
Background Primary hepatic neuroendocrine tumors (PH-NETs) are extremely rare and
unknown. Because of its rarity, its prognosis features and influencing factors are not well …

[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 …

Efficacy of chemotherapy versus transcatheter arterial chemoembolization in patients with advanced primary hepatic neuroendocrine carcinoma and an analysis of the …

S Li, M Niu, W Deng, N Li, C Wei… - Cancer Management …, 2021 - Taylor & Francis
Background Primary hepatic neuroendocrine carcinoma (PHNEC) is a rare liver tumor, and
there is no clear therapeutic recommendation for patients with advanced PHNEC. This study …

Diagnostic dilemma in a patient with history of medullary thyroid carcinoma and abnormal serum liver enzymes; a case report with six years follow up

F Rahmani, M Tohidi, F Azmoudeh-Ardalan… - BMC Endocrine …, 2023 - Springer
Background Medullary thyroid carcinoma (MTC) is a neuroendocrine tumor that originates
from parafollicular C-cells. Calcitonin (Ctn) and carcinoembryonic antigen (CEA) are useful …

Primary hepatic neuroendocrine tumors: clinical characteristics and imaging features on contrast-enhanced ultrasound and computed tomography

R Li, CL Tang, D Yang, XH Zhang, P Cai, KS Ma… - Abdominal …, 2016 - Springer
Objective Primary hepatic neuroendocrine tumor (PHNET) is an extremely rare liver
neoplasm, and its clinical characteristics and imaging features are not well understood. The …

[HTML][HTML] Primary hepatic neuroendocrine tumor case with a preoperative course of 26 years: A case report and literature review

XF Meng, YW Pan, ZB Wang… - World Journal of …, 2018 - ncbi.nlm.nih.gov
Primary hepatic neuroendocrine tumor (PHNET) is an extremely rare liver tumor. Patients
often have no clinical symptoms or have only non-specific symptoms, such as abdominal …