Abstract Library

#4445 Pancreatico-duodenal gastrinomas: Surgical management and late results – 50 years' experience in a single centre

Introduction: Gastrinomas are one of the less frequent and elusive variety of neuroendocrine tumours (NET) of the upper digestive tract and pancreas, clinically expressed with a Zollinger-Ellison syndrome (ZES), possibly associated to a Multiple Endocrine Neoplasia type 1 (MEN1).

Conference:

Presenting Author:

Authors: Milanetto A, Veronese E, de Carlo E, Pasquali C,

Keywords: gastrinoma, men1, net,

#3694 Enucleation of pancreatic neuroendocrine neoplasms – Short- and long-term results in open surgery in a single center

Introduction: Surgery plays a key role in the treatment of pancreatic neuroendocrine tumors (pNET). Enucleation combine a radical resection with sparing of healthy pancreatic parenchyma.

Conference:

Presenting Author: Milanetto A

Authors: Milanetto A, Gabriel G, de Carlo E, Pasquali C,

Keywords: insulinoma, gastrinoma, enucleation,

#2925 A Single Centre Experience of Open Surgery for Pancreatic Insulinomas on 88 Patients

Introduction: Insulinomas are functioning pancreatic neuroendocrine neoplasms (NENs), typically small and with a benign clinical course in more than 90% of cases.

Conference: 17th Annual ENETSConcerence (2020)

Presenting Author:

Authors: Milanetto A, Da Broi M, Liço V, De Carlo E, Pedrazzoli S,

Keywords: pancreas, insulinoma, surgery,

#983 Vipomas: Report of Three Cases in Ten Years

Introduction: VIPoma is a rare neuroendocrine tumor (NET) with an incidence of one in 10 million per year. Most cases arise within the pancreas, with others reported in the lungs, colon, liver, adrenals, and neuroganglia.

Conference: 11th Annual ENETSConcerence (2014)

Presenting Author:

Authors: Moletta L, Milanetto A, Liço V, De Carlo E, Alaggio R,

Keywords: vipoma, neuroendocrine tumors, pancreatic resections,

#958 Hypoglycemic Syndrome Recurrence after Surgical Removal of a Pancreatic Neuroendocrine Adenoma

Introduction: A 56-year-old woman was submitted to caudal pancreatectomy for an insulin-secreting adenoma suspected by MRI and fast test positivity at 38th hour. Intraoperative US excluded other pancreatic lesions but tissue analysis described a 8mm neuroendocrine well-differentiated tumor and the surrounding pancreatic tissue exhibited characteristics of nesidioblastosis. Five months after surgery, she still reported episodes of hypoglycemia requiring diazoxide therapy and she was admitted to our department.

Conference: 11th Annual ENETSConcerence (2014)

Presenting Author: De Carlo E

Authors: Bettini V, Martini C, Ferrata M, Battocchio M, Zanchetta E,

Keywords: insulinoma, nesidiblastosis, hypoglycemia,