Abstract
We report two cases of infants who presented seizures and persistent hypoglycemia. In both infants, we established diagnosis of persistent hypoglycemia by hyperinsulinism (PHH); glycemic/insulinic ratio was > 0.3, and we found no pancreatic changes by means of other diagnostic procedures. The medical treatment consisted of hydrocortisone, diazoxide, and octreotide without response. Definitive treatment made was sub-total pancreatectomy; postoperatory evolution was satisfactory, and the histologic report showed changes in Langerhans islet of nesidioblastosis. We conclude that PHH and glucose/insulin ratio > 0.3 indicates that surgical treatment with pancreatectomy should not be delayed.
Translated title of the contribution | Persistent hyperinsulinemic hypoglycemia. Two case reports |
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Original language | Spanish |
Pages (from-to) | 409-414 |
Number of pages | 6 |
Journal | Cirugia y Cirujanos |
Volume | 72 |
Issue number | 5 |
State | Published - 2004 |
Externally published | Yes |