Abstract
Persistent hyperinsulinemic hypoglycemia of infancy or congenital hyperinsulinism of the neonate is a rare condition that may cause severe neurologic damage if the disease is unrecognized or inadequately treated. Current treatment aims to restore normal blood glucose levels by providing a carbohydrate-enriched diet and drugs that inhibit insulin secretion. If medical treatment fails, then surgery is required. Because congenital hyperinsulinism may be caused either by diffuse involvement of pancreatic β-cells or by a focal cluster of abnormal β-cells, the extent of pancreatectomy varies. We report on 2 patients with a focal form of the disease for whom diagnosis was made with laparoscopy. Laparoscopic enucleation of the lesion was curative. Copyright © 2004 by the American Academy of Pediatrics.
| Original language | English |
|---|---|
| Pages (from-to) | e520-e522 |
| Journal | Pediatrics |
| Volume | 114 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Oct 2004 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Congenital hyperinsulinism
- Laparoscopy
- Neurodevelopmental outcome
- Pancreatectomy
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