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

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 pain and abdominal mass. The clinical manifestations, disease development, treatment methods, and treatment outcomes of PHNET...

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Detalles Bibliográficos
Autores principales: Meng, Xiang-Fei, Pan, Ying-Wei, Wang, Zhan-Bo, Duan, Wei-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021771/
https://www.ncbi.nlm.nih.gov/pubmed/29962820
http://dx.doi.org/10.3748/wjg.v24.i24.2640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021771/
https://www.ncbi.nlm.nih.gov/pubmed/29962820
http://dx.doi.org/10.3748/wjg.v24.i24.2640

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