| Literature DB >> 33641016 |
Valentina Ferraro1, Michele Tedeschi2, Letizia Laera3, Michele Ammendola4, Umberto Riccelli5, Nicola Silvestris6, Alba Fiorentino7, Giammarco Surico3, Riccardo Inchingolo8, Francesco Decembrino9, Nicola de Angelis10, Riccardo Memeo2.
Abstract
OPINION STATEMENT: Pancreatic neuroendocrine tumours (PNETs) are a rare and heterogeneous group of tumours with various clinical manifestations and biological behaviours. They represent approximately 2-4% of all pancreatic tumours, with an incidence of 2-3 cases per million people. PNETs are classified clinically as non-functional or functional, and pancreatic resection is recommended for lesions greater than 2 cm. The surgical approach can involve "typical" and "atypical" resections depending on the number, size and location of the tumour. Typical resections include pancreaticoduodenectomy, distal pancreatectomy enucleation and, rarely, total pancreatectomy. Atypical resections comprise central pancreatectomies or enucleations. Minimally invasive pancreatic resection has been proven to be technically feasible and safe in high-volume and specialized centres with highly skilled laparoscopic surgeons, with consolidated benefits for patients in the postoperative course. However, open and minimally invasive pancreatic surgery remains to have a high rate of complications; there is no specific technical contraindication to minimally invasive pancreatic surgery, but an appropriate patient selection is crucial to obtain satisfactory clinical and oncological outcomes.Entities:
Keywords: Laparoscopy; Minimally invasive surgery; Pancreatic surgery; Pnets
Mesh:
Year: 2021 PMID: 33641016 DOI: 10.1007/s11864-021-00824-5
Source DB: PubMed Journal: Curr Treat Options Oncol ISSN: 1534-6277