PANCREATIC NEUROENDOCRINE TUMORS: SURGICAL RESECTION

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Surgical Management of Pancreatic Neuroendocrine Tumors

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Pancreatic Endocrine Tumors (PNETs) represent a rare, but important subset of pancreatic neoplasms. These tumors account for 2–4% of all clinically detected pancreatic tumors. Their overall incidence is approximately 1 of 100 000 people per year [1,2]. PNETs consist of single or multiple benign or malignant neoplasms and are associated with multiple endocrine neoplasia type 1 (MEN1) in 10– 20% ...

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Aggressive surgical resection in the management of pancreatic neuroendocrine tumors: when is it indicated?

BACKGROUND Pancreatic neuroendocrine tumors (PNETs) comprise a heterogeneous group of neoplasms for which treatment is variable, depending on the clinical stage. Despite this diversity, surgery remains the gold standard in the management of PNETs. This paper discusses whether aggressive surgical intervention is indicated for PNETs and investigates what prognostic factors may assist in predictin...

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Pancreatic neuroendocrine tumors are usually indolent (slow-growing) by nature and develop over the course of many years. Pancreatic neuroendocrine tumors are usually more indolent, with better prognosis than adenocarcinoma of the pancreas (Carriaga & Henson, 1995). However, aggressive, fast growing pancreatic neuroendocrine tumors exist and different types of pancreatic neuroendocrine tumors e...

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ژورنال

عنوان ژورنال: ABCD. Arquivos Brasileiros de Cirurgia Digestiva (São Paulo)

سال: 2019

ISSN: 2317-6326,0102-6720

DOI: 10.1590/0102-672020180001e1428