Surgical Management and Long-Term Evaluation of Pancreatic Neuroendocrine Tumors.
Surg Clin North Am
; 104(4): 891-908, 2024 Aug.
Article
en En
| MEDLINE
| ID: mdl-38944507
ABSTRACT
Pancreatic neuroendocrine tumors (PNETs) arise from neuroendocrine cells and are a rare class of heterogenous tumors with increasing incidence. The diagnosis, staging, treatment, and prognosis of PNETs depend heavily on identifying the histologic features and biological mechanisms. Here, the authors provide an overview of the diagnostic workup (biomarkers and imaging), grade, and staging of PNETs. The authors also explore associated genetic mutations and molecular pathways and describe updated guidelines on surgical and systemic treatment modalities.
Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Neoplasias Pancreáticas
/
Tumores Neuroendocrinos
Límite:
Humans
Idioma:
En
Año:
2024
Tipo del documento:
Article