Nephrocalcinosis
Introduction
Nephrocalcinosis is characterised by deposits of calcium salts in the kidney tissue. As usual, this occurs in the interstitium in the medullary areas of the kidney. The condition is often associated with calcium kidney stones (calcium phosphate or calcium oxalate). Otherwise, nephrocalcinosis can also lead to acute or chronic kidney failure or be randomly detected in an x-ray examination. Nephrocalcinosis can have different causes and the prognosis of the kidneys is based on the underlying cause.
Causes
Nephrocalcinosis is due to increased secretion of calcium salts in the urine (calcium phosphate or calcium oxalate). In the medullary areas where the osmolality is high and the concentration of salts exceeds the saturation level for solubility. Citrate is a natural inhibitor of precipitation of calcium salts and hypocitraturia can contribute to the condition.
Table of the most common causes of nephrocalcinosis
Causes |
Examples |
Hypercalciuria with hypercalcemia | Primary hyperparathyroidism |
| Sarcoidosis |
| Hypervitaminosis D |
Hypercalciuria without hypercalcemia | Distal renal tubular acidosis |
| Medullary sponge kidney |
| Loop diuretics |
| Congenital tubulopathies |
| Chronic hypokalemia |
Hyperphosphaturia | |
Hyperoxaluria | Congenital: primary |
| Acquired: fat malabsorption (short bowel syndrome) |
Histopathology
Tubular, intracellular and interstitial calcium deposits. Interstitial inflammation, interstitial fibrosis and tubular atrophy can be the consequences of calcium deposits. (Picture fom Helge)
Urinalysis
Hematuria can occur simultaneously with kidney stones. Otherwise, the urine is usually normal without proteinuria.
Prognosis and treatment
The treatment is targeted towards the underlying cause. Increasing the fluid intake to dilute the urine is recommended to all. Administration of citrate can increase the solubility of calcium salts and is recommended when the urine pH < 7.
The prognosis is based on the underlying cause
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