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Unusual case of hypercalcemia in a patient with primary steroid-resistant nephrotic syndrome
Authors: Ľ. Kováčiková ml.; Ľ. Tichá; M. Chocholová; Ľ. Podracká
Authors‘ workplace: Detská klinika Lekárskej fakulty Univerzity Komenského a Detskej fakultnej nemocnice s poliklinikou, Bratislava
Published in: Čes-slov Pediat 2017; 72 (1): 39-44.
Category: Case Report
Overview
Calcium homeostasis imbalance occurs frequently in patients with nephrotic syndrome. Characteristic finding is hypocalcemia that is usually a result of severe hypoalbuminemia (pseudohypocalcemia). Other contributing factor is a urinary loss of vitamin D binding proteins with subsequent vitamin D deficiency that decreases intestinal calcium absorption.
We describe the unusual case of hypercalcemia in a 12-year old girl with primary steroid-resistant nephrotic syndrome caused by focal segmental glomerulosclerosis. The patient was treated with corticosteroids and multiple 2-line imunosupressive medications without achievement of complete remission. Hypercalcemia was unexpected finding at the state of fully developed laboratory signs of nephrotic syndrome. Hypercalcemia persisted despite discontinuation of vitamin D and calcium supplementation administered for corticosteroid induced osteoporosis. Ultrasonography and positron emission tomography of parathyroid glands raised suspicion for parathyroid adenoma. Histological evaluation following adenoma exstirpation confirmed the diagnosis.Key words:
nephrotic syndrome, hypercalciemia, parathyroid adenoma
Sources
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Neonatology Paediatrics General practitioner for children and adolescents
Article was published inCzech-Slovak Pediatrics
2017 Issue 1-
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