Long-Term Treatment of an Infant with Nesidioblastosis Using a Somatostatin Analogue
- 22 January 1987
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 316 (4) , 222-223
- https://doi.org/10.1056/nejm198701223160417
Abstract
To the Editor: Nesidioblastosis is a condition of inappropriate insulin secretion.1 2 3 Treatment consists of normalizing the glucose level with insulin-suppressive drugs or glucagon. Subtotal or even total removal of the pancreas may be necessary. A female Moroccan newborn was admitted to the hospital directly after birth with asphyxia and convulsions. Laboratory examination revealed hypoglycemia (14 mg per deciliter) with an elevated serum insulin level (76 mU per liter). Glucose infusions with diazoxide treatment did not restore normoglycemia. When the child was four weeks of age, subtotal pancreatectomy was performed; histologic examination showed nesidioblastosis. When she was 8.5 months old, hypoglycemia . . .Keywords
This publication has 3 references indexed in Scilit:
- Nesidioblastosis of the pancreas: definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia.Archives of Disease in Childhood, 1981
- Somatostatin treatment of insulin excess due to β-cell adenoma in a neonateThe Journal of Pediatrics, 1980
- Nesidioblastosis: the pathologic basis of persistent hyperinsulinemic hypoglycemia in infants. Morphologic and quantitative analysis of seven cases based on specific immunostaining and electron microscopyDiabetes, 1977