Answers are grounded in this paper and cite their sources.
Calcitonin reduces hypercalcemia in a neonate with congenital mesoblastic nephroma, suggesting a rapid treatment option.
Subcutaneous administration of calcitonin is effective in the preoperative management of hypercalcemia associated with congenital mesoblastic nephroma (CMN). The short onset of action (within 2 hours) and duration (6 to 8 hours), makes it a viable alternative to bisphosphonates (action 48 hours and duration of 7 to 14 days). A 15-day-old late preterm, male, presented with dehydration, failure to thrive and a large abdominal mass. On admission, he was hypertensive, and a firm mass was palpable in the abdomen. Severe hypercalcemia was noted on the blood work. An abdominal ultrasound shows a large 9×8 cm dominant solid right renal mass. Echo and electrocardiography (ECG or EKG) were normal. The patient initially received IV hydration, nicardipine and furosemide. The hypercalcemia persisted after 24 hours of treatment; thus, one dose of calcitonin (6 units/kg subcutaneously) was given, resulting in a decrease in serum calcium to the upper limits of normal within 4 hours. The patient then underwent a successful radical right uretero-nephrectomy. Pathology reported congenital mesoblastic nephroma (CMN) of the cellular type. This is the third case report describing the use of calcitonin for a likely PTH-rP-mediated severe hypercalcemia in a neonate with CMN.
No takes yet. Share an insight, caveat, or question.
Gálvez et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: