Primary mesenteric neuroendocrine tumor: Case report

Alejandro González-Muñoz, Edgar Javier Aguirre-Salamanca, Natalia Andrea Rivera-Rincón, José Gabriel Rodríguez-Narvaez, Pablo González-Sierra, Camilo Ramírez-Giraldo

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction and importance: Neuroendocrine tumors most frequently originate from the gastrointestinal tract (GIT). Their presentation in tissues other than the GIT and pancreas is usually due to metastatic involvement from lesions at these sites. There have been a few cases of neuroendocrine tumors identified in tissues such as the mesentery and peritoneum, without identification of a primary lesion supporting their origin as metastasis. Case presentation: We present the case of a patient with abdominal pain, in whom a primary mesenteric neuroendocrine tumor was identified. The patient completed one year of follow-up without identification of an additional lesion. Case Reported in line with the SCARE criteria. Clinical discussion: This is a rare condition with few reports in the literature, without significant changes in its classification or management. Conclusion: The search for a primary lesion and follow-up are essential to characterize the presence of primary mesenteric neuroendocrine tumors.

Original languageEnglish
Article number108517
Pages (from-to)108517
JournalInternational Journal of Surgery Case Reports
Volume109
DOIs
StatePublished - Aug 2023

Keywords

  • Mesenteric tumor
  • Neuroendocrine tumors
  • Primary mesenteric tumor

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