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.
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Scott, A. T., & Howe, J. R. (2019, August 1). Evaluation and Management of Neuroendocrine Tumors of the Pancreas. Surgical Clinics of North America. W.B. Saunders. https://doi.org/10.1016/j.suc.2019.04.014
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