A lifetime of hypercalcemia and hypercalciuria, finally explained.

CONTEXT

Hypercalcemia, hypercalciuria, and recurrent nephrolithiasis are all common clinical problems. This case report illustrates a newly described but possibly not uncommon cause of this presenting complex.

OBJECTIVE

We report on a patient studied for over 30 years, with the diagnosis finally made with modern biochemical and genetic tools.

DESIGN AND SETTING

This study consists of a case report and review of literature conducted in a University Referral Center.

PATIENT AND INTERVENTION

A single patient with hypercalcemia, hypercalciuria, and recurrent nephrolithiasis was treated with low-calcium diet, low vitamin D intake, prednisone, and ketoconazole.

MAIN OUTCOME MEASURE

We measured the patient's clinical and biochemical response to interventions above.

RESULTS

Calcium absorption measured by dual isotope absorptiometry was elevated at 37.4%. Serum levels of 24,25-dihydroxyvitamin D were very low, as measured in two laboratories (0.62 ng/mL [normal, 3.49 ± 1.57], and 0.18 mg/mL). Genetic analysis of CYP24A1 revealed homozygous mutation E143del previously described. The patient's serum calcium and renal function improved markedly on treatment with ketoconazole but not with prednisone.

CONCLUSIONS

Chronic hypercalcemia, hypercalciuria, and/or nephrolithiasis may be caused by mutations in CYP24A1 causing failure to metabolize 1,25-dihydroxyvitamin D.