[HTML][HTML] An insight on functioning pancreatic neuroendocrine neoplasms

M Bevere, A Gkountakos, FM Martelli, A Scarpa… - Biomedicines, 2023 - mdpi.com
Pancreatic neuroendocrine neoplasms (PanNENs) are rare neoplasms arising from islets of
the Langerhans in the pancreas. They can be divided into two groups, based on peptide …

Synchronous Insulinoma and Glucagonoma: A Review of the Literature

C Damaskos, D Dimitroulis, A Garmpi, EA Antoniou… - in vivo, 2023 - iv.iiarjournals.org
Background/Aim: Pancreatic neuroendocrine tumors (PNETs) are pancreatic neoplasms
with neuroendocrine features, divided into functioning and non-functioning. The non …

[HTML][HTML] A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas

C Smirne, GM Giacomini, AM Berton, B Pasini… - Journal of …, 2024 - Springer
Purpose Multiple endocrine neoplasia type 1 (MEN1) is a hereditary endocrine syndrome
caused by pathogenic variants in MEN1 tumor suppressor gene. Diagnosis is commonly …