Hypercalcaemia
Patients today are unlikely to present with gross bone disease or severe renal calculi as a consequence of untreated primary hyperparathyroidism. General practitioners who are aware of the telltale signs and symptoms of hypercalcaemia can identify this disorder before gross bone abnormalities or renal problems have had time to develop. The widespread use of multichannel analysers in clinical biochemistry laboratories can detect unsuspected hypercalcaemia even before symptoms become apparent. A high serum calcium concentration may be an unexpected finding in a patient in any clinic or hospital ward, as the symptoms of hypercalcaemia are non-specific. All such findings should be followed up.
Diagnosis
The commonest causes of hypercalcaemia are primary hyperparathyroidism and hypercalcaemia of malignancy.
A diagnostic decision chart is shown in Figure 36.1. Primary hyperparathyroidism is most often due to a single parathyroid adenoma, which secretes PTH independently of feedback control by plasma calcium. Hypercalcaemia associated with malignancy is the commonest cause of a high calcium in a hospital population. Some tumours secrete a protein called PTHrP (parathyroid hormone-related protein), which has PTH-like properties.
Rarer causes of hypercalcaemia include:
Inappropriate dosage of vitamin D or metabolites, e.g. in the treatment of hypoparathyroidism or renal disease or due to self-medication.
Granulomatous diseases (such as sarcoidosis or tuberculosis) or certain tumours (such as lymphomas) synthesize 1,25-dihydroxycholecalciferol.
Thyrotoxicosis very occasionally leads to increased bone turnover and hypercalcaemia.
Thiazide therapy: the hypercalcaemia is usually mild.

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