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Robotic Enucleation of an Intra-Pancreatic Insulinoma in the Pancreatic Head
Published on: January 3, 2020
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Insulinoma With Concomitant Insulin Antibodies
Anira Iqbal1, David T Broome2, Vinni Makin2
1Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio.
AACE Clinical Case Reports
|July 26, 2021
Summary
This case report details a rare instance of insulinoma coexisting with insulin antibodies. This finding highlights a novel presentation of hypoglycemia, crucial for physicians to recognize.
Area of Science:
- Endocrinology
- Oncology
- Immunology
Background:
- Insulinoma, a rare pancreatic neuroendocrine tumor, typically presents with hypoglycemia.
- Insulin antibodies are usually associated with exogenous insulin use or autoimmune conditions.
- The simultaneous occurrence of insulinoma and insulin antibodies is exceptionally rare.
Observation:
- A patient presented with severe symptomatic hypoglycemia and was diagnosed with insulinoma.
- Laboratory tests revealed elevated insulin and proinsulin levels with a low insulin-to-C-peptide ratio, indicative of endogenous hyperinsulinism.
- The patient also exhibited a high titer of immunoglobulin G insulin antibodies.
Findings:
- A biopsy-proven neuroendocrine tumor (insulinoma) was identified via endoscopic ultrasound.
- Successful treatment involved prednisone and radiofrequency ablation for the insulinoma.
- The patient achieved remission with steroid taper and no recurrence of symptoms.
Implications:
- This case underscores the importance of considering insulinoma in patients with unexplained hypoglycemia, even in the presence of insulin antibodies.
- The coexistence of insulinoma and insulin antibodies presents a unique diagnostic and therapeutic challenge.
- This report expands the understanding of rare endocrine disorders and their complex presentations.
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