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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2018
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| Materias: | |
| 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 |