Insulinoma: Metastatic Recurrence 38 Years Following Initial Diagnosis in Pregnancy

Author:

Preston Christopher A12ORCID,Sachithanandan Nirupa13ORCID,Sim Ie-Wen12345,van Heerden Jon678,Farrell Stephen910

Affiliation:

1. Department of Endocrinology & Diabetes, St Vincent’s Hospital Melbourne , Fitzroy, Victoria 3065 , Australia

2. Department of Endocrinology & Diabetes, Western Health , Melbourne, Victoria 3021 , Australia

3. Department of Medicine, The University of Melbourne , Fitzroy, Victoria 3065 , Australia

4. Department of Endocrinology & Diabetes, Monash Health and Eastern Health , Melbourne, Victoria 3168 , Australia

5. Department of Medicine, Monash University , Clayton, Victoria 3168 , Australia

6. Department of Surgery, Mayo Medical School , Rochester, MN 55905 , USA

7. Department of Surgery, Mayo Medical School, Mayo Clinic , Rochester, MN 55905 , USA

8. Department of Surgery, Medical University of South Carolina , Charleston 29425 , USA

9. Department of Surgery, St Vincent’s Hospital Melbourne , Fitzroy, Victoria 3065 , Australia

10. Department of Surgery, Austin Health , Heidelberg, Victoria 3084 , Australia

Abstract

Abstract A case of recurrent insulinoma spanning 4 decades is described. Following a delayed diagnosis, hyperinsulinemic hypoglycemia was confirmed in a 24-year-old woman during early pregnancy. Initial surgery, culminating in subtotal pancreatectomy, was noncurative. A 1-cm insulinoma was subsequently resected from the head of the pancreas postpartum, with postoperative resolution of hypoglycemia. However, 32 years later, the patient experienced a recurrence of hypoglycemic symptoms. Eventually, a subcentimeter extrapancreatic lesion was identified anterior to the pancreatic head on gallium-68 DOTA-Exendin-4 positron emission tomography/computed tomography. In 2022, a third operation was performed, with excision of a 4 × 3 mm tumor adjacent to the pancreatic head, and histology confirming insulinoma. She was again cured of symptoms.

Publisher

The Endocrine Society

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