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Updated: Jun 28, 2026

Isolation of Human Islets from Partially Pancreatectomized Patients
Published on: July 30, 2011
Noninsulinoma pancreatogenous hypoglycemia syndrome in a Saudi male
Abdullah M Karawagh1, Layla S Abdullah, Abdelhamid M Gasim
1Department of Medicine, King Khalid National Guard Hospital, PO Box 9515, Jeddah, Kingdom of Saudi Arabia. a_karawagh@yahoo.com
Abstract:
Nesidioblastosis is focal or diffuse islet hyperplasia leading to hyperinsulinism with subsequent hypoglycemia in the absence of insulinoma, usually described in neonates and infancy. We described the first adult case of nesidioblastosis in Saudi Arabia and the Gulf region. The diagnosis and treatment of the condition can be very difficult and challenging. Despite the fact that our patient responded initially to surgical treatment, his hypoglycemic symptoms occasionally recurred and needed adjunctive medical treatment. Although initially thought to affect only infants and children, cases of nesidioblastosis can affect adults and pose a diagnostic and therapeutic challenge to the clinicians.
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