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 hypercalcemiaPrimary hyperparathyroidism
Sarcoidosis
Hypervitaminosis D
Hypercalciuria without hypercalcemiaDistal renal tubular acidosis
Medullary sponge kidney
Loop diuretics
Congenital tubulopathies
Chronic hypokalemia
Hyperphosphaturia
HyperoxaluriaCongenital: 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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