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Updated: May 6, 2026

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Insulinoma presenting with cardiac arrest and cardiomyopathy
Arthi Thirumalai1, Ximena A Levander, Somnath Mookherjee
1Internal Medicine Residency Program, University of Washington, Seattle, Washington, USA.
Insights
A rare case of insulinoma caused severe hypoglycemia, leading to cardiac arrest and dilated cardiomyopathy. Surgical removal of the pancreatic tumor cured hypoglycemia and improved heart function.
Area of Science:
- Cardiology
- Endocrinology
- Oncology
Background:
- Insulinoma, a rare pancreatic tumor, causes hyperinsulinemic hypoglycemia.
- Hypoglycemia can precipitate cardiac events and myocardial dysfunction.
- Dilated cardiomyopathy is a serious cardiac condition with various potential causes.
Observation:
- A 33-year-old woman presented with ventricular fibrillation cardiac arrest and severe hypoglycemia (1.83 mmol/L).
- Cardiac catheterization revealed dilated cardiomyopathy with reduced ejection fraction (26%) and normal coronary arteries.
- Continuous dextrose infusion was necessary, suggesting an underlying cause for hypoglycemia and cardiomyopathy.
Findings:
- Whipple's triad was confirmed, and a 72-hour fast provided biochemical evidence of insulinoma.
- Imaging localized a pancreatic tumor, which was resected and confirmed as insulinoma.
- Pancreaticoduodenectomy cured the hypoglycemia, and the patient's ejection fraction improved to 41% within 4 months.
Implications:
- This case highlights insulinoma as a potential cause of unexplained dilated cardiomyopathy and cardiac arrest.
- High insulin levels may directly affect cardiac function by closing K(ATP) channels.
- Hypoglycemia-induced catecholamine surges and QT prolongation can contribute to ventricular remodeling and arrhythmias.
Abstract:
A 33-year-old woman presented with ventricular fibrillation cardiac arrest and was found to have a blood glucose of 1.83 mmol/L. Cardiac catheterisation revealed a dilated left ventricle with an ejection fraction (EF) of 26% and angiographically normal coronary arteries. Continuous dextrose infusion was required to treat hypoglycaemia, which prompted consideration of insulinoma as a possible cause for her cardiomyopathy. Whipple's triad was demonstrated; a 72 h fast provided biochemical evidence of insulinoma, and imaging localised a tumour in her pancreas. The tumour was resected and pathology confirmed insulinoma; pancreaticoduodenectomy cured her hypoglycaemia. No alternate cause of cardiomyopathy was found and 4 months after surgery her EF improved to 41%. High insulin levels can close cardiac K(ATP) channels associated with dilated cardiomyopathy; the catecholamine surge from hypoglycaemia may also contribute to ventricular remodelling. Hypoglycaemia can cause QT segment prolongation, and may have precipitated fibrillation in this patient's arrhythmia-prone myocardium.
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