Renal Calcifications
Eva Ilse Rubio, MD
DIFFERENTIAL DIAGNOSIS
Common
Miscellaneous Hypercalcemia/Hypercalciuria
Chronic Diuretic Therapy
Renal Tubular Acidosis
Medullary Sponge Kidney
Tamm-Horsfall Proteins (Mimic)
Less Common
Chronic Glomerulonephritis
Papillary Necrosis
Infection/Infarction/Trauma
Oxalosis/Hyperoxaluria
Alport Syndrome
Rare but Important
Salt-Wasting Nephropathies
Bartter, Gitelman Syndromes
Malignancies
Wilms Tumor
Sarcoma
Renal Cell Carcinoma
Poisoning/Toxicity
Tuberculosis
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Distribution
Medullary nephrocalcinosis
Abnormal calcium deposition within renal medullary pyramids
Within interstitium or distal tubules
Represents between 85-95% of all cases of nephrocalcinosis
Cortical nephrocalcinosis
Abnormal calcium deposition within renal cortex
Represents minority of cases of nephrocalcinosis
Basic definitions
Nephrocalcinosis: Abnormal calcium deposition within renal parenchyma
Nephrolithiasis: Formation/presence of calculi within upper renal collecting system (renal calyces or renal pelvis)
Often calcium compounds but not exclusively
Calculi may or may not obstruct
Urolithiasis: Presence of calculi in mid to lower urinary tract (ureters, urinary bladder); obstructing or nonobstructing
Helpful Clues for Common Diagnoses
Miscellaneous Hypercalcemia/Hypercalciuria
Distribution: Medullary region
Numerous etiologies: Dietary, pharmaceutical, immobilization, metabolic, steroid use, familial, idiopathic, sarcoid, endocrine abnormalities
US more sensitive than radiographs
Calcifications on US have variable appearance: Punctate, coarse, granular, round, linear; ± shadowing
Chronic Diuretic Therapy
Distribution: Medullary region
Results from use of loop diuretics, commonly furosemide (Lasix)
Associated with hypercalciuria
More common in premature infants; many cases will resolve several months after discontinuation
Renal Tubular Acidosis
Distribution: Medullary region
Most reliably identified by US
Calcifications may be deposited at periphery of medulla or may occupy entire medullary pyramid
Small or sparse calcifications may not demonstrate posterior acoustic shadowing
Results from proximal tubule defect in bicarbonate resorption
Urine: May have hypercalciuria, urolithiasis
Blood: May have secondary hyperparathyroidism &/or hypophosphatemia
Medullary Sponge Kidney
Distribution: Medullary region
Primary abnormality is cystic/patulous dilatation of distal tubules
Urinary stasis in tubules results in precipitation of urinary calcium crystals
Distribution of calcifications may be patchy/asymmetric
Intravenous pyelogram reveals linear opacities of accumulated contrast material within dilated distal tubules
Tamm-Horsfall Proteins (Mimic)
Helpful Clues for Less Common Diagnoses
Chronic Glomerulonephritis
Distribution: Nearly exclusively cortical
Granular, cortical intratubular
Papillary Necrosis
Distribution: Medullary region, particularly papillae
Consider medical background
Analgesic use, sickle cell, dehydration, renal vein thrombosis, infection, liver disease
Infection/Infarction/Trauma
Distribution: Predominantly cortical, unilateral or bilateral, depending on underlying etiology
Unilateral: Prior infection, focal vascular injury, trauma, renal vein thrombosis
Bilateral: Systemic vascular compromise, disseminated infection (TB), chronic glomerulonephritis, hemolytic uremic syndrome
Oxalosis/Hyperoxaluria
Distribution: Predominantly medullary, may be cortical
Underlying cause may be genetic, enteric, dietary, or mild/idiopathic
Alport Syndrome
Distribution: Classically cortical
Multiple genetic forms; associated with variable severity of deafness, hypertension, hematuria, ocular disease
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