Evidence mapPaperPMID 42130933Full record

ArticleEuropean journal of case reports in internal medicine2026

GLP-1 Receptor Agonist Associated Unmasking of Insulinoma.

Eden Simonov, Rina Berger, Olga Shishkina, Alexander Sivokha, Dror Cantrell

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Article in European journal of case reports in internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Eden SimonovMaccabi Healthcare Services (MHS), Bat Yam, Israel.
Rina BergerInternal Medicine 'C', Shamir Medical Center, Zerifin, Israel, affiliated to the Gray Faculty of Medical & Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Olga ShishkinaDepartment of Radiology, Shamir Medical Center, Zerifin, Israel, affiliated to the Gray Faculty of Medical & Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Alexander SivokhaInternal Medicine 'C', Shamir Medical Center, Zerifin, Israel, affiliated to the Gray Faculty of Medical & Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Dror CantrellInternal Medicine 'C', Shamir Medical Center, Zerifin, Israel, affiliated to the Gray Faculty of Medical & Health Sciences, Tel Aviv University, Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Insulinoma is a rare functional pancreatic neuroendocrine tumour and the most common cause of endogenous hyperinsulinaemic hypoglycaemia in adults. Diagnosis is frequently delayed due to non-specific and intermittent symptoms, and a high index of suspicion is needed. Case description: We report the case of a 40-year-old non-diabetic woman who presented with recurrent episodes of weakness shortly after initiation of a glucagon-like peptide-1 receptor agonist (GLP-1RA). Laboratory evaluation demonstrated inappropriately elevated insulin and C-peptide levels during documented hypoglycaemic events, consistent with endogenous hyperinsulinaemia. Autoimmune and exogenous causes were excluded. Imaging studies identified a 2 cm hypervascular pancreatic lesion, with functional imaging confirming somatostatin receptor avidity consistent with an insulin-secreting tumour. The patient was initially treated with diazoxide as a bridge to definitive management. She subsequently underwent laparoscopic distal pancreatectomy, with histopathology confirming a well-differentiated pancreatic neuroendocrine tumour (WHO Grade 1). Following surgery, hypoglycaemia resolved completely. Conclusion: This case highlights the potential of GLP-1 receptor agonist therapy to unmask an insulinoma. Many benign insulinomas exhibit abundant expression of GLP-1 receptors. While a high index of suspicion remains essential, awareness of the emerging association between the incretin-based therapies and unexplained hypoglycaemia may facilitate earlier diagnosis. LEARNING POINTS: Hypoglycaemia is a rare but significant clinical event, and thorough evaluation is mandatory.Widely used GLP-1RA medications are glucose-dependent and therefore rarely cause hypoglycaemia; occurrence should prompt clinical suspicion for an underlying cause.Benign insulinomas express high levels of GLP-1 receptors; consequently, GLP-1 RAs may induce otherwise unexplained hypoglycaemia and can be used as tracers to localise difficult to detect tumours.

Indexed as

glucagon-like peptide-1 receptor agonists (GLP-1RAs)hypoglycaemiaInsulinoma

Identifiers

PMID42130933
PMCPMC13166994

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.