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NESIDIOBLASTOSIS IN AN ADULT WITH SHORT GUT SYNDROME AND TYPE 2 DIABETES.

AbstractOBJECTIVE:
Adult nesidioblastosis is characterized by endogenous hyperinsulinemia typically causing post-prandial hypoglycemia, and most commonly occurs post-Roux-en-Y gastric bypass.
METHODS:
We report a unique case of nesidioblastosis occurring in a 67-year-old female.
RESULTS:
A 5-year history of symptomatic hypoglycemia occurred in a patient with short bowel syndrome and type 2 diabetes mellitus (T2DM) managed previously with a glucagon-like peptide 1 (GLP-1) agonist, which achieved significant weight loss. Continuous glucose monitoring captured 42 hypoglycemia episodes in a 2-week period, and following an oral glucose tolerance test there was the suggestion of a hyperinsulinemia state. She was managed with an open distal pancreatectomy, and subsequently required medical therapy to maintain euglycemia.
CONCLUSION:
We present the first case of nesidioblastosis occurring in a patient with short bowel syndrome, pre-existing T2DM managed with a GLP-1 agonist which achieved significant weight loss, all of which we speculate could have predisposed to hypoglycemia and development of nesidioblastosis.
AuthorsMimi Wong, Luke Conway, Caroline Cooper, Ashim Sinha, Nirjhar Nandi
JournalAACE clinical case reports (AACE Clin Case Rep) 2019 Nov-Dec Vol. 5 Issue 6 Pg. e375-e379 ISSN: 2376-0605 [Electronic] United States
PMID31967075 (Publication Type: Case Reports)
CopyrightCopyright © 2019 AACE.

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