Malignant Insulinoma Arising From Nonfunctioning Pancreatic Neuroendocrine Tumor
- PMID: 38445216
- PMCID: PMC10914231
- DOI: 10.14309/crj.0000000000000954
Malignant Insulinoma Arising From Nonfunctioning Pancreatic Neuroendocrine Tumor
Abstract
Pancreatic neuroendocrine tumors are rare neoplasms characterized into nonfunctioning (NF-PNET) and functioning (F-PNET) subtypes. F-PNETs typically involve overt symptoms related to excessive hormone secretion but may rarely present first as NF-PNETs with delayed transformation. We present a patient with known NF-PNET with liver metastases who developed hypoglycemia 2 years after initial diagnosis due to malignant insulinoma. Hypoglycemia was refractory to continuous dextrose but improved temporarily after diazoxide and hepatic artery embolization. Malignant insulinomas are usually metastatic at presentation and portend poor prognosis. Hypoglycemia may be medically managed with steroids, somatostatin analogues, and diazoxide, along with therapies to reduce tumor burden.
Keywords: diazoxide; hepatic artery embolization; insulinoma; liver metastases; pancreatic neuroendocrine tumor.
© 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology.
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