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Updated: Jul 1, 2025

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Robotic Enucleation of an Intra-Pancreatic Insulinoma in the Pancreatic Head
Published on: January 3, 2020
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Malignant Insulinoma Arising From Nonfunctioning Pancreatic Neuroendocrine Tumor
Ritodhi Chatterjee1, Basim Ali1, Son H Nguyen2
1Department of Internal Medicine, Baylor College of Medicine, Houston, TX.
ACG Case Reports Journal
|March 6, 2024
Summary
Rare pancreatic neuroendocrine tumors (PNETs) can transform. This case shows a nonfunctioning PNET (NF-PNET) progressing to a malignant insulinoma, causing severe hypoglycemia refractory to initial treatment.
Area of Science:
- Endocrinology
- Oncology
- Gastroenterology
Background:
- Pancreatic neuroendocrine tumors (PNETs) are rare neoplasms with functioning (F-PNET) and nonfunctioning (NF-PNET) subtypes.
- While F-PNETs present with hormone hypersecretion symptoms, NF-PNETs can rarely transform into functioning tumors.
- Malignant insulinomas, a type of F-PNET, are often metastatic at diagnosis and associated with a poor prognosis.
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