Functional Localization of Adult-Onset Idiopathic Nesidioblastosis

Author:

Hercus Jess C.1ORCID,Pasha Pouneh2,Al Lawati Sadiq3,Kim Peter4,Mattman Andre5ORCID,Webber Douglas5,Thompson David M.3ORCID

Affiliation:

1. Department of Biological Sciences, Simon Fraser University, Burnaby, British Columbia, Canada

2. Division of Internal Medicine, Department of Medicine, University of British Columbia, 5913-1081 Burrard St., Vancouver, British Columbia V6Z 1Y6, Canada

3. Division of Endocrinology, Department of Medicine, University of British Columbia, 2775 Laurel Street, 4th Floor, Vancouver, British Columbia V5Z 1M9, Canada

4. Division of General Surgery, Department of Medicine, University of British Columbia, 2775 Laurel Street, 11th Floor, Vancouver, British Columbia V5Z 1M9, Canada

5. Division of Pathology and Laboratory Medicine, Department of Medicine, University of British Columbia, G227-2211 Wesbrook Mall, Vancouver, British Columbia V6T 2B5, Canada

Abstract

Nesidioblastosis is a rare pancreatic disorder involving enlarged beta cells throughout the pancreas, causing elevated insulin production. We present the case of a 53-year-old woman with the initial symptom of fasting hypoglycemia. No pancreatic lesions were indicated on computed tomography and magnetic resonance imaging scans, and an octreotide scan was negative for insulinoma. Selective arterial calcium stimulation (SACST) showed increased insulin production from the stimulation of 3 out of 5 arteries. The SACST results suggested a diagnosis of nesidioblastosis, which was confirmed by histopathology after a subtotal distal pancreatectomy. The patient has normal glucose tolerance after surgery with no further problems of hypoglycemia, indicating that this is a rare case of nesidioblastosis extending only partially through the pancreas.

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism

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