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

BACKGROUND: Primary hepatic neuroendocrine tumors (PHNETs), a group of neuroendocrine neoplasms, are extremely rare. There are only few case reports about PHNETs in the literature. The lack of large samples and multicenter research results in poor diagnostic and therapeutic approaches. AIM: To discu...

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Detalles Bibliográficos
Autores principales: Wang, Hao-Hao, Liu, Zhao-Chen, Zhang, Gong, Li, Lu-Hao, Li, Lin, Meng, Qing-Bo, Wang, Pei-Ju, Shen, Dong-Qi, Dang, Xiao-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Retrospective Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510005/
https://www.ncbi.nlm.nih.gov/pubmed/33005296
http://dx.doi.org/10.4251/wjgo.v12.i9.1031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510005/
https://www.ncbi.nlm.nih.gov/pubmed/33005296
http://dx.doi.org/10.4251/wjgo.v12.i9.1031

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