| Literature DB >> 31255207 |
Aaron T Scott1, James R Howe2.
Abstract
Pancreatic neuroendocrine tumors are a diverse group of neoplasms with a generally favorable prognosis. Although they exhibit indolent growth, metastases are seen in roughly 60% of patients. Pancreatic neuroendocrine tumors may produce a wide variety of hormones, which are associated with dramatic symptoms, but the majority are nonfunctional. The diagnosis and treatment of these tumors is a multidisciplinary effort, and management guidelines continue to evolve. This review provides a concise summary of the presentation, diagnosis, surgical management, and systemic treatment of pancreatic neuroendocrine tumors.Entities:
Keywords: Neuroendocrine tumor; PNET; Pancreas; Surgery
Mesh:
Year: 2019 PMID: 31255207 PMCID: PMC6601637 DOI: 10.1016/j.suc.2019.04.014
Source DB: PubMed Journal: Surg Clin North Am ISSN: 0039-6109 Impact factor: 2.741