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- W3129419570 endingPage "948.e4" @default.
- W3129419570 startingPage "938" @default.
- W3129419570 abstract "Pancreatic neuroendocrine tumors (PNETs) are a heterogeneous group of neoplasms that arise from islet cells and can occur sporadically or as part of a hereditary syndrome. While the majority are nonfunctional, some can produce hormones that contribute to a unique array of symptoms, and distinguishing between functional and nonfunctional PNETs is paramount. A multidisciplinary team is utilized in the evaluation and management. Although newer imaging and treatment modalities that utilize radioactive substances linked to somatostatin analogues are becoming more prevalent, surgery remains the mainstay of treatment. Prognosis is generally favorable and mainly depends upon tumor burden, histopathologic characteristics, and etiology. This chapter focuses on the evaluation and management of PNETS, with particular attention to the pediatric population." @default.
- W3129419570 created "2021-03-01" @default.
- W3129419570 creator A5042756847 @default.
- W3129419570 creator A5063357178 @default.
- W3129419570 creator A5074456866 @default.
- W3129419570 date "2021-01-01" @default.
- W3129419570 modified "2023-09-25" @default.
- W3129419570 title "Pancreatic Neuroendocrine Tumors" @default.
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