Abstract
Hypercalcemia in children is a rare condition and may result from various etiologies, such as genetic, metabolic, iatrogenic causes and malignancy. In some malignancies, parathyroid hormone related protein (PTHrP) can mimic the physiological effects of parathyroid hormone (PTH) and cause hypercalcemia. In this report , we present a rare case of hypercalcemia secondary to juvenile fibroadenoma, a benign breast tumor. A 14-year-old girl presented with the complaint of a solid breast mass. Following evaluation with ultrasonography and trucut biopsy, a diagnosis of 14x8 cm juvenile fibroadenoma was made. Laboratory examination revealed hypercalcemia (13.9 mg/dL) and high PTHrP (>24.8 ng/L) although the patient was asymptomatic. Despite pharmacological treatment, the patient continued to experience persistent hypercalcemia and subsequently underwent a successful surgical excision. Serum calcium and PTHrP levels normalized postoperatively. Hypercalcemia secondary to malignancy in children is rare and calcium elevation is usually mild-moderate and asymptomatic. In this case, PTHrP was elevated in a girl with breast fibroadenoma, demonstrating that hypercalcemia can also be associated with benign tumors. The follow-up data after surgical treatment supports the suggestion that PTHrP-related hypercalcemia does not always indicate a poor prognosis. This case demonstrates the importance of considering benign tumors, such as juvenile fibroadenoma, as a potential cause of hypercalcemia in adolescents.
Keywords: Hypercalcemia, juvenile fibroadenoma, parathyroid hormone-related protein
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