Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor

Pancreatic neuroendocrine tumors (pNETs) are rare pancreatic neoplasms and are even more uncommon in the pediatric patients, thus leading to a lack of clinical research on diagnosis and management in this population. The purpose of this report is to review relevant literature and discuss a rare occu...

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Main Authors: Whitney Elks, Jessa Rose Li, Alexander Zajack, Lance Horner, Alan Ikeda, Charles St Hill, Michael Scheidler, Shirong Chang
Format: Article
Language:English
Published: Elsevier 2023-01-01
Series:Journal of Pediatric Surgery Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213576622003438
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author Whitney Elks
Jessa Rose Li
Alexander Zajack
Lance Horner
Alan Ikeda
Charles St Hill
Michael Scheidler
Shirong Chang
author_facet Whitney Elks
Jessa Rose Li
Alexander Zajack
Lance Horner
Alan Ikeda
Charles St Hill
Michael Scheidler
Shirong Chang
author_sort Whitney Elks
collection DOAJ
description Pancreatic neuroendocrine tumors (pNETs) are rare pancreatic neoplasms and are even more uncommon in the pediatric patients, thus leading to a lack of clinical research on diagnosis and management in this population. The purpose of this report is to review relevant literature and discuss a rare occurrence of a non-functioning pNET in a pediatric patient. This is a report of an 11-year-old male who presented with symptomatic anemia and was found to have a 6 cm mass near the pancreatic head with erosion into the duodenum. Surgical biopsy demonstrated a non-functioning pNET. He was successfully managed with complete surgical resection via a standard pancreaticoduodenectomy without evidence of recurrence after 1 year follow up. Further multi-institutional prospective studies or meta-analyses are warranted to further explore optimal management in the pediatric population.
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spelling doaj.art-4f372dd5f6504c1595c5bff0fcd7b6e92022-12-22T02:59:48ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662023-01-0188102516Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumorWhitney Elks0Jessa Rose Li1Alexander Zajack2Lance Horner3Alan Ikeda4Charles St Hill5Michael Scheidler6Shirong Chang7Kirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United States; Corresponding author. Department of Surgery, Kirk Kerkorian School of Medicine at the University of Nevada Las Vegas, 1707 W Charleston Blvd Suite 110, Las Vegas, NV, 89102, United States.Kirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United StatesKirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United StatesKirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United StatesCure 4 the Kids Foundation, 1 Breakthrough Way, Las Vegas, NV, 89135, United StatesKirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United StatesKirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United StatesKirk Kerkorian School of Medicine, University of Nevada, Las Vegas, Department of Surgery, 1707 W. Charleston Blvd, Suite 110, Las Vegas, NV, 89102, United StatesPancreatic neuroendocrine tumors (pNETs) are rare pancreatic neoplasms and are even more uncommon in the pediatric patients, thus leading to a lack of clinical research on diagnosis and management in this population. The purpose of this report is to review relevant literature and discuss a rare occurrence of a non-functioning pNET in a pediatric patient. This is a report of an 11-year-old male who presented with symptomatic anemia and was found to have a 6 cm mass near the pancreatic head with erosion into the duodenum. Surgical biopsy demonstrated a non-functioning pNET. He was successfully managed with complete surgical resection via a standard pancreaticoduodenectomy without evidence of recurrence after 1 year follow up. Further multi-institutional prospective studies or meta-analyses are warranted to further explore optimal management in the pediatric population.http://www.sciencedirect.com/science/article/pii/S2213576622003438Pancreatic neuroendocrine tumorPancreaticoduodenectomyWhipple procedurePediatric
spellingShingle Whitney Elks
Jessa Rose Li
Alexander Zajack
Lance Horner
Alan Ikeda
Charles St Hill
Michael Scheidler
Shirong Chang
Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor
Journal of Pediatric Surgery Case Reports
Pancreatic neuroendocrine tumor
Pancreaticoduodenectomy
Whipple procedure
Pediatric
title Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor
title_full Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor
title_fullStr Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor
title_full_unstemmed Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor
title_short Pancreaticoduodenectomy in 11-year-old male with a non-functional pancreatic neuroendocrine tumor
title_sort pancreaticoduodenectomy in 11 year old male with a non functional pancreatic neuroendocrine tumor
topic Pancreatic neuroendocrine tumor
Pancreaticoduodenectomy
Whipple procedure
Pediatric
url http://www.sciencedirect.com/science/article/pii/S2213576622003438
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