Logo del repository
  1. Home
 
Opzioni

New Concepts in Pathology

Massimo Milione
•
Laura Cattaneo
•
Alessandro Mangogna
2021
  • book part

Abstract
Neuroendocrine neoplasms (NENs) originate from the diffuse neuroendocrine system and, therefore, can arise in every part of the body. In two-thirds of cases, they rise in the gastroenteropancreatic (GEP) tract. NENs represent a heterogeneous group with variable biological and clinical characteristics. They are usually considered rare neoplasms when compared in terms of incidence with the corresponding non-neuroendocrine neoplasms. NENs represent about 1–2% of the total neoplasms of the gastrointestinal (GI) tract but are of particular diagnostic, prognostic, and therapeutic interest. The main negative prognostic factors of NENs are the site of the primary tumor [pancreatic NENs (PanNENs) generally have a worse prognosis than NENs in the rectum], the stage according to TNM and the World Health Organization (WHO) histopathological classification, which expresses both the morphological aspect of the tumor cells and their proliferative activity in terms of the number of mitoses or proliferation index (Ki-67). In PanNENs, for example, Ki-67 labeling index correlates significantly with overall survival and also with disease progression in patients with advanced neoplasms and with tumor recurrence in patients undergoing curative surgery. GEP-NENs are all potentially malignant and are distinguished in tumors and carcinomas. Tumor grading is defined by both morphology and the proliferative index of the tumor (mitotic index and Ki-67). According to the aforesaid grading rule, WHO 2019 distinguishes: G1-NETs (well-differentiated morphology, <2 mitosis/10 HPF, and/or Ki-67 <3%); G2-NETs (well-differentiated morphology, 2–20 mitosis/10 HPF, and/or Ki-67 between 3% and 20%); G3-NET (well-differentiated morphology, >20 mitosis/10 HPF, and/or Ki-67 >20%); and NEC (poorly differentiated morphology, >20 mitosis/10 HPF, and/or Ki-67 >20%). MiNENs (mixed neuroendocrine non-neuroendocrine neoplasms) are neoplasms in which the two components, neuroendocrine and non-neuroendocrine, are both represented in at least 30% of the entire tumor.
DOI
10.1007/978-3-030-72830-4_3
WOS
WOS:000625808300001
Archivio
http://hdl.handle.net/11368/3025076
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85160731137
https://link.springer.com/chapter/10.1007/978-3-030-72830-4_3
Diritti
open access
license:copyright editore
license:digital rights management non definito
license uri:iris.pri02
license uri:iris.pri00
FVG url
https://arts.units.it/request-item?handle=11368/3025076
Soggetti
  • Neuro Endocrine Neopl...

  • Diagnosis and treatme...

  • Predictive biomarkers...

  • Biological and clinic...

google-scholar
Get Involved!
  • Source Code
  • Documentation
  • Slack Channel
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your nstitution's web identity.

Need professional help?

The original creators of DSpace-CRIS at 4Science can take your project to the next level, get in touch!

Realizzato con Software DSpace-CRIS - Estensione mantenuta e ottimizzata da 4Science

  • Impostazioni dei cookie
  • Informativa sulla privacy
  • Accordo con l'utente finale
  • Invia il tuo Feedback