… Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disorder, is … of pancreatic
neuroendocrine tumours (P-NETs) in association with parathyroid and pituitary tumours. P…

… was found in patients with larger tumors. This review summarizes key concepts in
managing PNETs in patients with MEN1. Keywords: Pancreatic neuroendocrine tumors (PNETs), …

… MEN1 patients with MEN1 mutations leading to CHES1-… MEN1) is an autosomal dominant
inherited disorder classically characterized by the development of neuroendocrine neoplasms …

… Pancreatic neuroendocrine tumors (pNETs) are highly prevalent in patients with multiple
endocrine neoplasia type 1 (MEN1), and metastatic disease is an important cause of …

… tumors at a young age, with primary hyperparathyroidism due to parathyroid adenomas,
neuroendocrine tumors (… MEN1 patients are also at risk of adrenal tumors, lung NETs, thymic …

… We selected 20 studies with a pooled population of 105 MEN1 patients with pNENs. Females
were 58.5%, median age was 44 years (18–73). TNM stage at diagnosis was stage I–II in …

… Patients and Controls Eight neuroendocrine tumors from six MEN1 patients were included
in this study. The patient ages were 19, 22, 42, 51, 57, and 57 years at the time of surgery (…

… -related br-NETs do not significantly decrease overall survival of MEN1 patients; (6)
operated and metastasis-free patients had better survival; (7) surgery is safe as there were no …

… , patients were selected from the Dutch national MEN1 database of the DutchMEN1 Study
Group (DMSG). All MEN1 patients … In each UMC, MEN1 patients were identified by a standard …

… conclude that in patients with MEN1 undergoing resection of … neuroendocrine and non-neuroendocrine
tumors. This necessitates validation of evidence from sporadic pNETs in MEN1 …