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Updated: Apr 30, 2026

Improving IV Insulin Administration in a Community Hospital
Published on: June 11, 2012
Management challenges in a child with hyperinsulinemic hypoglycemia
Deepti Chaturvedi1, Rajesh Khadgawat1, Jeyaraman Kanakamani1
1Department of Endocrinology, All India Institute of Medical Sciences, New Delhi, India.
Insights
Malignant insulinoma, a rare pediatric cancer, was diagnosed in an 18-month-old child with islet cell hyperplasia. Despite surgical interventions, the child developed metastatic disease, representing the youngest reported case.
Area of Science:
- Pediatric Oncology
- Endocrinology
- Surgical Gastroenterology
Background:
- Malignant insulinoma is an exceptionally rare tumor in pediatric populations.
- Hyperinsulinemic hypoglycemia in infants can be caused by various conditions, including rare pancreatic tumors.
Purpose of the Study:
- To report the youngest known case of malignant insulinoma with metastatic disease in a child.
- To highlight the diagnostic and management challenges of pediatric malignant insulinoma.
Main Methods:
- Case presentation of an 18-month-old child with recurrent hyperinsulinemic hypoglycemia.
- Diagnostic imaging including Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET) scan.
- Surgical management (enucleation and subtotal pancreatectomy) and histopathological confirmation with immunostaining.
Main Results:
- The patient presented with hyperinsulinemic hypoglycemia, initially treated with tumor enucleation and later subtotal pancreatectomy.
- Despite surgical interventions, metastatic insulinoma to the liver was confirmed.
- This case represents the youngest reported instance of metastatic malignant insulinoma in a child.
Conclusions:
- Malignant insulinoma, though rare, should be considered in pediatric cases of persistent hyperinsulinemic hypoglycemia.
- Early and accurate diagnosis, coupled with aggressive management, is crucial for pediatric patients with malignant insulinoma.
- Metastatic potential underscores the need for vigilant monitoring and advanced imaging in affected children.
Abstract:
Malignant insulinoma is very rare in children. Herein, we present a case of a child with malignant insulinoma along with islet cell hyperplasia. She initially presented with features of hyperinsulinemic hypoglycemia at 18 mo of age. Magnetic resonance imaging (MRI) of the abdomen showed a mass at the junction of the head and body of the pancreas. The tumor was enucleated. Five months later symptoms of hypoglycemia recurred. A subtotal pancreatectomy was performed. She continued to have hypoglycemia, although less frequently. She was put on increasing doses of diazoxide. Seven months later, MRI of the abdomen and a PET scan revealed metastatic deposits in the liver, which were confirmed by histopathology and immunostaining. To the best of our knowledge, this is the youngest child with metastatic insulinoma reported so far.
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