Some malignant adrenal masses may rarely contain intracytoplasmic lipid and lose signal on
out-of-phase images:
Some malignant adrenal masses may rarely contain intracytoplasmic lipid and lose signal on
out-of-phase images:
Pheochromocytoma/paragangliomas are associated with several syndromes:
Glomus tumours
Paragangliomas of the head and neck are generally called glomus tumors and may be
associated with the tympanic membrane (glomus tympanicum), the jugular foramen
(glomus jugulare), the carotid body (called a carotid body tumor), or the vagus nerve
(glomus vagale).
differential of
echogenic renal mass
Angiomyolipoma (AML). An echogenic renal mass is suggestive of AML (due to internal fat
content), particularly when isoechoic to the sinus fat.
Renal calculus.
Milk of calcium, caused by crystals precipitating out of supersaturated solution.
Sloughed papilla, secondary to papillary necrosis, may appear as an echogenic mass in the
collecting system (often calcified).
Intrarenal gas (e.g., infection, recent nephrostomy tube placement).
Malignant neoplasm (atypical appearance).
Unilateral delayed nephrogram:
Acute ureteral obstruction.
Renal artery stenosis.
Renal vein thrombosis/compression.
Acute pyelonephritis.
Bilateral persistent nephrogram:
Systemic hypotension.
Acute tubular necrosis.
Contrast nephropathy.
Acute urate nephropathy.
Proteinuria (e.g., myeloma kidney).
Bilateral obstructive uropathy.
Unilateral prolonged (hyperdense) nephrogram:
Acute ureteral obstruction.
Renal artery stenosis.
Renal vein thrombosis/compression.
Unilateral striated nephrogram:
Acute urinary obstructi on (unilateral).
Acute pyelonephriti s.
Renal infarct.
Renal vein thrombosis or vasculiti s.
Renal contusion (typically focal).
Acute radiati on therapy.
Bilateral striated nephrograms:
Acute urinary obstructi on (bilateral).
Acute pyelonephriti s.
Acute tubular necrosis.
Hypotension.
Autosomal recessive polycysti c kidney disease
(ARPKD).
unilateral enlarged kidney
unilateral enlarged kidney includes:
Pyelonephriti s.
Acute ureteral obstructi on.
Renal vein thrombosis.
Compensatory hypertrophy.
differential of
medullary
nephrocalcinosis
Hyperparathyroidism is the most common cause of medullary nephrocalcinosis.
Sarcoidosis (hypercalcemia).
Type 1 renal tubular acidosis (distal type).
Medullary sponge kidney is caused by ectatic tubules in the medullary pyramids that can
lead to stasis and stone formation.
Papillary necrosis.
In children, treatment with furosemide (Lasix) can lead to medullary nephrocalcinosis.
cortical nephrocalcinosis include:
Acute cortical necrosis.
Chronic glomerulonephritis.
Chronic transplant rejection.
Hyperoxaluria.
Alport syndrome (hereditary nephropathy and deafness).
Autosomal recessive
polycystic kidney disease.
Papillary Necrosis
The commonly used POSTCARD mnemonic may be
helpful to remember all causes:
Pyelonephriti s.
Obstructi on.
Sickle cell disease.
Tuberculosis.
Cirrhosis.
Analgesics (NSAIDS).
Renal vein thrombosis.
Diabetes mellitus.
Hydrpnephrosis
Common causes of hydronephrosis
Obstructive (more common):
Obstructing calculus is the most common cause.
Ureteral or bladder malignancy.
External compression of the ureter by a mass or
retroperitoneal fibrosis.
Non-obstructive:
VUR
(post-procedural or Pregnancy (usually right > left).
VHL
Clear cell RCCs
Renal Cysts
Birt-Hogg-Dubé
Chromophobe RCCs
Oncocytomas
Tuberous sclerosis
Slightly increased
risk of RCC
Bilateral AMLs
Renal cysts
Hereditary
papillary RCC
Papillary RCCs
HLRCC
Multi ple renal
cancer subtypes,
papillary most
common
Sickle cell trait
Medullary RCCs