Pancreatic neuroendocrine tumors (pNETs) are frequently malignant (50-80%, except for insulinoma) and may show an aggressive course with metastases to the liver as well as more distant sites. These heterogeneous neoplasms include functioning tumors, which secrete a variety of peptide hormones, and non-functioning tumors (up to 90% of pNETs), which often show metastases at the time of diagnosis.

Therapy for metastatic pancreatic neuroendocrine tumors / Rossi, R. E.; Massironi, S.; Conte, D.; Peracchi, M.. - In: ANNALS OF TRANSLATIONAL MEDICINE. - ISSN 2305-5839. - 2:1(2014), pp. 1-12. [10.3978/j.issn.2305-5839.2013.03.01]

Therapy for metastatic pancreatic neuroendocrine tumors

S. Massironi;
2014-01-01

Abstract

Pancreatic neuroendocrine tumors (pNETs) are frequently malignant (50-80%, except for insulinoma) and may show an aggressive course with metastases to the liver as well as more distant sites. These heterogeneous neoplasms include functioning tumors, which secrete a variety of peptide hormones, and non-functioning tumors (up to 90% of pNETs), which often show metastases at the time of diagnosis.
2014
pancreatic neuroendocrine tumors (pNETs)
duodenocephalopancreasectomy
liver metastases
liver transplantation
liver-directed therapies
somatostatin analogues
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/172062
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