@article{10.37349/etat.2023.00133,
abstract = {Neuroendocrine tumours (NETs) are a rare type of tumours that arise from the neuroendocrine cells which are distributed throughout the body. Of all the gastrointestinal tumours only 1–2% account for NETs. They have an extremely low incidence of 0.17% arising in the intrahepatic bile duct epithelium. Majority of hepatic NETs occur as a result of metastases from the primary NETs. Most cases of primary hepatic NET (PHNET) present as a solid nodular mass. However, predominantly cystic PHNET is extremely rare which mimics other cystic space-occupying lesions clinically and radiologically as seen in this case.},
author = {Londhe, Mangesh and Garg, Sakshi and Gurwale, Sushama and Gore, Charusheela},
doi = {10.37349/etat.2023.00133},
journal = {Exploration of Targeted Anti-tumor Therapy},
pages = {266--272},
title = {{Cystic presentation of primary hepatic neuroendocrine tumour: a case report with a brief review of literature}},
url = {https://www.explorationpub.com/Journals/etat/Article/1002133},
volume = {4},
year = {2023},
number = {2}
}