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Laparoscopic total pancreatectomy for multiple endocrine neoplasia type 1 syndrome‐associated multifocal, non‐functioning pancreatic neuroendocrine tumor: A case report
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AbstractPancreatic neuroendocrine tumors are rare, accounting for less than 3% of all pancreatic tumors. Although laparoscopic pancreas‐preserving surgery for managing sporadic pancreatic neuroendocrine tumors has been described in the literature, laparoscopic total pancreatectomy has rarely been reported. We present a 30‐year‐old man who was incidentally diagnosed with multiple endocrine neoplasia type 1 syndrome with parathyroid hyperplasia and a non‐functioning pancreatic neuroendocrine tumor. He underwent laparoscopic total pancreatectomy with splenectomy. This report highlights the technical details of laparoscopic total pancreatectomy, which appears to be a feasible and safe option in select cases.
Wiley
Title: Laparoscopic total pancreatectomy for multiple endocrine neoplasia type 1 syndrome‐associated multifocal, non‐functioning pancreatic neuroendocrine tumor: A case report
Description:
AbstractPancreatic neuroendocrine tumors are rare, accounting for less than 3% of all pancreatic tumors.
Although laparoscopic pancreas‐preserving surgery for managing sporadic pancreatic neuroendocrine tumors has been described in the literature, laparoscopic total pancreatectomy has rarely been reported.
We present a 30‐year‐old man who was incidentally diagnosed with multiple endocrine neoplasia type 1 syndrome with parathyroid hyperplasia and a non‐functioning pancreatic neuroendocrine tumor.
He underwent laparoscopic total pancreatectomy with splenectomy.
This report highlights the technical details of laparoscopic total pancreatectomy, which appears to be a feasible and safe option in select cases.
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