Hyperinsulinemic Hypoglycemia Due to an Insulinoma in a 2-Year-Old Child

Insulinomas are rare insulin-secreting tumors that most commonly affect adults. A 26-month-old child presented to her local emergency department with severe hypoglycemia. Initial workup was consistent with hyperinsulinemic hypoglycemia. Over the course of 10 months, multiple therapies for hyperinsulinism (HI) were trialed without significant benefit. Genetic testing for genes associated with HI was negative. At age 35 months, the patient was transferred to our center for further treatment. She underwent several imaging tests that revealed a lesion on her pancreas concerning for an insulinoma. The patient underwent surgical intervention to enucleate the lesion. Histopathological review of the specimen confirmed a benign, well-circumscribed insulinoma. A postoperative fasting test proved the patient was cured and she was discharged without the need for further glucose monitoring.

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Publication Details

Journal
JCEM Case Reports
Published
2024-08-14
DOI
https://doi.org/10.1210/jcemcr/luae161
Citations
1
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
Field-Weighted Citation Impact
0.39
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article

Hyperinsulinemic Hypoglycemia Due to an Insulinoma in a 2-Year-Old Child

Lauren Mitteer, Diva D. De León, Katherine Lord, Tricia Bhatti et al.
1 citations
JCEM Case Reports
Neuroendocrine Tumor Research Advances
0.39
article

Hyperinsulinemic Hypoglycemia Due to an Insulinoma in a 2-Year-Old Child

Lauren Mitteer, Diva D. De León, Katherine Lord, Tricia Bhatti, N. Scott Adzick, Lisa J. States
article en
1 citations

Abstract

Insulinomas are rare insulin-secreting tumors that most commonly affect adults. A 26-month-old child presented to her local emergency department with severe hypoglycemia. Initial workup was consistent with hyperinsulinemic hypoglycemia. Over the course of 10 months, multiple therapies for hyperinsulinism (HI) were trialed without significant benefit. Genetic testing for genes associated with HI was negative. At age 35 months, the patient was transferred to our center for further treatment. She underwent several imaging tests that revealed a lesion on her pancreas concerning for an insulinoma. The patient underwent surgical intervention to enucleate the lesion. Histopathological review of the specimen confirmed a benign, well-circumscribed insulinoma. A postoperative fasting test proved the patient was cured and she was discharged without the need for further glucose monitoring.

JCEM Case ReportsVol. 2(9)
Children's Hospital of Philadelphia (US), University of Pennsylvania (US)
Good health and well-being
Openalex Percentile: Top 34%
Neuroendocrine Tumor Research Advances
0.39
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Hyperinsulinemic Hypoglycemia Due to an Insulinoma in a 2-Year-Old Child — Lauren Mitteer, Diva D. De León, et al. · JCEM Case Reports (2024) | TGRS Research Map | TGRS