Year 2022 / Volume 114 / Number 11
Letter
Cystic pancreatic neuroendocrine tumors: a multidisciplinary diagnostic challenge

691-692

DOI: 10.17235/reed.2022.8709/2022

Sergio Bazaga, Jair Morales-Alvarado, Francesc Bas-Cutrina, Eva Fernandez Monclús, Inma Méndez Coca,

Abstract
Cystic pancreatic neuroendocrine tumours (cPNETs) are an uncommon diagnosis, representing less than 10% of all cystic neoplasms. They tend to affect patients aged between 30 and 60 years, with no differences between the sexes. Herein we present the case of a woman aged 75 years with a history of AHT, DM2 and CKF. Given symptoms of abdominal pain, toxic syndrome and altered hepatic analyses, the patient underwent an abdominal CT, which showed a solid mass with neoproliferative appearance in the pancreatic tail, along with a small, non-specific portacaval adenopathy. Consequently, an echo-endoscopy (USE) was performed to complete the study.
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Citation tools
Bazaga S, Morales-Alvarado J, Bas-Cutrina F, Fernandez Monclús E, Méndez Coca I. Cystic pancreatic neuroendocrine tumors: a multidisciplinary diagnostic challenge. 8709/2022


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Publication history

Received: 13/02/2022

Accepted: 19/04/2022

Online First: 24/05/2022

Published: 07/11/2022

Article revision time: 60 days

Article Online First time: 100 days

Article editing time: 267 days


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