| Literature DB >> 15466080 |
Monique De Vroede1, N M A Bax, Klaus Brusgaard, Mark J Dunne, Floris Groenendaal.
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 beta-cells or by a focal cluster of abnormal beta-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.Entities:
Mesh:
Year: 2004 PMID: 15466080 DOI: 10.1542/peds.2003-1180-L
Source DB: PubMed Journal: Pediatrics ISSN: 0031-4005 Impact factor: 7.124