Recombinant Human GH in Managing Refractory Hypoglycemia in a Young Patient With Embryonal Rhabdomyosarcoma.
Aditya V Belamkar1, Viral N Shah2,3, Palak Patadia2
1Department of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
JCEM Case Reports
|July 29, 2025
Summary
Non-islet cell tumor hypoglycemia (NICTH) is a rare condition caused by tumors releasing insulin-like growth factor 2 (IGF-2). Recombinant human growth hormone (rhGH) effectively managed severe hypoglycemia in a patient with metastatic rhabdomyosarcoma.
Area of Science:
- Endocrinology
- Oncology
Background:
- Non-islet cell tumor hypoglycemia (NICTH) is a rare paraneoplastic syndrome.
- It is typically mediated by the overproduction of insulin-like growth factor 2 (IGF-2).
Observation:
- A 24-year-old male with metastatic embryonal rhabdomyosarcoma presented with severe symptomatic hypoglycemia.
- Initial management with corticosteroids and dextrose was unsuccessful.
- Laboratory findings suggested an IGF-2-mediated pathway despite a suboptimal IGF-2/IGF-1 ratio.
Findings:
- Recombinant human growth hormone (rhGH) therapy was initiated.
- Somatropin (rhGH) administration led to the resolution of hypoglycemia.
- Patients were successfully weaned off dextrose and steroid support.
Implications:
- This case demonstrates the potential utility of rhGH in managing NICTH, particularly in non-resectable malignancies.
- Individualized treatment strategies are crucial for managing complex cases of NICTH.
- Further research into rhGH for NICTH is warranted.
Related Concept Videos
Hypoglycemia and Glucagon
338
Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
338
Insulin: Dosing Regimen and Adverse Effects
262
Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
262
Glucagon-like Receptor Agonists
420
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
420


