Laparoscopic diagnosis and cure of hyperinsulinism in two cases of focal adenomatous hyperplasia in infancy

Monique De Vroede, N. M A Bax, Klaus Brusgaard, Mark J. Dunne, Floris Groenendaal

    Research output: Contribution to journalArticlepeer-review

    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 languageEnglish
    Pages (from-to)e520-e522
    JournalPediatrics
    Volume114
    Issue number4
    DOIs
    Publication statusPublished - Oct 2004

    Keywords

    • Congenital hyperinsulinism
    • Laparoscopy
    • Neurodevelopmental outcome
    • Pancreatectomy

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