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Synchronous Peripancreatic Lymph Node Gastrinoma and Gastric Neuroendocrine Tumor Type 2

Authors
Lee, Hee WooChung, Jun-WonKim, Yoon JaeKwon, Kwang AhnKim, Eui JooKim, Keon KukLee, Woon KiSym, Sun Jin
Issue Date
Sep-2016
Publisher
KOREAN SOC GASTROINTESTINAL ENDOSCOPY
Keywords
Gastrinoma; Neuroendocrine tumors; Zollinger-Ellison syndrome
Citation
CLINICAL ENDOSCOPY, v.49, no.5, pp.483 - 487
Journal Title
CLINICAL ENDOSCOPY
Volume
49
Number
5
Start Page
483
End Page
487
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/7938
DOI
10.5946/ce.2016.008
ISSN
2234-2400
Abstract
A 34-year-old man was referred to our hospital with gastric polypoid lesions and biopsy-confirmed neuroendocrine tumor (NET). Computed tomography (CT) revealed a 3x3.5x8-cm retroperitoneal mass behind the pancreas, with multiple hepatic metastases. His serum gastrin level was elevated to 1,396 pg/mL. We performed a wedge resection of the stomach, a right hemi-hepatectomy, and a retroperitoneal mass excision. After careful review of the clinical, radiological, histopathological, and immunohistochemical findings, peripancreatic gastrinoma, and synchronous gastric NET were ultimately diagnosed. We reviewed a CT scan that had been performed 6 years previously after surgery for a duodenal perforation. There was no evidence of gastric or hepatic lesions, but the retroperitoneal mass was present at the same site. Had gastrinoma been detected earlier, our patient could have been cured using less invasive treatment. This case demonstrates how important it is to consider Zollinger-Ellison syndrome in patients with a recurrent or aggressive ulcer.
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