Pancreatic neuroendocrine tumors (pNETs) are characterized as a rare disease with an
incidence of less than 1 in 100,000 individuals per year, and accounts for 1% to 2% of all …

Endocrine tumors are neoplasms arising from endocrine organs, regardless of whether the
tumor secretes hormones, and tumors producing or secreting hormones, regardless of the …

Genetics of neuroendocrine tumours is mainly related to major inherited syndromes which
predispose to the development of tumours in endocrine glands. Clinical and genetic studies …

Gastroenteropancreatic neuroendocrine tumors (GEP NETs) are relatively rare neoplasias
arising from the embryonic neural crest, neuroectoderm and endoderm. GEP NETs occur …

Simple Summary Neuroendocrine tumors are a rare group of neoplasms characterized by
strikingly heterogeneous pathological features and clinical behavior. The incidence and …

Pancreatic neuroendocrine tumors (pNETs) are uncommon cancers arising from pancreatic
islet cells. Here we report the analysis of gene mutation, copy number, and RNA expression …

While many organs not classified as endocrine glands, eg, fat, are now known to produce
hormones, cytokines, and other chemical messengers and secrete them directly into the …

Mixed neuroendocrine non-neuroendocrine neoplasms (MiNENs) represent a rare
diagnosis of the gastro-entero-pancreatic tract. Evidence from the current literature …

Abstract Background Neuroendocrine neoplasms (NENs) are rare tumours with variable
clinical behaviour. Their natural history is ideally best approached in large, multicentre and …

Background: Small intestinal neuroendocrine tumours (SI-NETs) represent a heterogeneous
group of rare tumours. In recent years, basic research in SI-NETs has attempted to unravel …