Searchable abstracts of presentations at key conferences in endocrinology

ea0027oc3.2 | Oral Communications 3 | BSPED2011

Clinical, genetic, histological and radiological heterogeneity of focal forms of congenital hyperinsulinism

Ismail Dunia , Kapoor Ritika , Smith Virpi , Ashworth Michael , Blankenstein Oliver , Pierro Agostino , Flanagan Sarah , Ellard Sian , Hussain Khalid

Congenital hyperinsulinism (CHI) is a cause of severe and persistent hypoglycaemia due to unregulated insulin secretion from pancreatic β-cells. Mutations in the ABCC8 and KCNJ11 genes are the most common cause of medically unresponsive CHI. Histologically there are three major subgroups, focal, diffuse and atypical. The pathophysiology of focal CHI is complex and involves a two hit process with the patient firstly inheriting a paternal ABCC8/KCNJ11 m...

ea0027oc3.3 | Oral Communications 3 | BSPED2011

Laparoscopic near total pancreatectomy for medically unresponsive diffuse congenital hyperinsulinism

Pierro Agostino , Ron Ori , Nah Shireen , Smith Virpi , Ashworth Michael , Eaton Simon , Coppi Paulo Dr , Hussain Khalid

Background: Congenital hyperinsulinism (CHI) is cause of severe hyperinsulinaemic hypoglycaemia in the neonatal and infancy periods. Histologically there are three major subgroups, diffuse, focal and atypical. Patients with diffuse CHI who are medically unresponsive will require a near total pancreatectomy. This has traditionally been performed using an open surgical approach.Aims: To report our experience of laparoscopic near total pancreatectomy for me...