Pediatric Body

Renal

  • If you do not see a kidney on one side you should keep the two major items in the differential

  • Solitary kidney (other side is just absent)

    • Be sure to look throughout the pelvis and abdomen first before stating this as kidney may be ectopic

  • Crossed fused renal ectopia

    • Basically the two kidneys are fused and located on one side

    • Will see abnormal tissue along the kidney which is the fused portion of the second kidney, will be more subtle than what a fused kidney looks like in horseshoe kidney for example

Calyceal Diverticulum

  • Will look like simple cyst but will show strong enhancement on delayed phase which represents communication between the diverticulum and the calyx

  • Layering of stones, calcium = highly suggestive of diverticulum

Ureterocele

  • Looks like filling defect in bladder

Bilateral Renal Agenesis

  • Suspect in newborns with pneumothorax

    • PTX raises concern for pulmonary hypoplasia

      • Pulmonary hypoplasia results from in utero oligohydraminos

        • Oligohydraminos —> renal agenesis

  • US will show

    • Flattened adrenal glands

    • Decompressed bladder (no urine being made)

  • Lethal

Duplicated collecting system

  • Can be partial or complete but when there are two collecting systems in one kidney

  • May be easy to see as they can have enlarged column of berlin

  • Highly associated with ureteroceles (if you see a ureterocele you need to look for duplicated system)

  • Upper moiety

    • typically has the ureterocele and becomes obstructed

    • Chronic obstruction results in cystic dysplasia and scarring

    • Upper ureter will insert ectopically

      • Will be lower and medial

  • Drooping lily sign

    • Only lower moiety fills so looks like a flower

  • Weigart-Meyer rule

    • the ectopic ureter will be medial and inferior

Multicystic Dysplastic Kidney

Ureteropelvic junction obstruction

  • Basically what the name says, there is an obstruction at the junction of the renal pelvis and ureter

  • Causes

    • Idiopathic

    • Compression by a vessel (can be a very small vessel and does not actually look like compression, just looks like the vessel is crossing the UPJ)

      • Look for accessory renal arteries which may be doing this

  • On imaging looks like severe hydro with dilatation of the ureter proximally

  • On multiphase urogram will likely not seen contrast in the affected ureter because there an obstruction but can see it in the calyces

  • Treatment

    • May resolve

    • Pyeloplasty (basically cut out the obstructed part and sew the other shit back together)

  • Can lead to renal cystic dysplasia

    • Basically chronic obstruction causes normal renal parenchyma to be replaced by communicating cysts which then becomes scar tissue

    • Different from MCDK because MCDK is congenital and renal pelvis is congenitally absent

Posterior Urethral Valves

  • Only males

  • If identified pre-natally will have oligohydramnios with pulmonary hypoplasia

  • Keyhole appearance

    • Due to dilatation of the bladder and posterior urethra

  • The bladder will typically have irregular contour due to chronic outlet obstruction - all because th ebladder is contracting against a closed door

    • Elongated

    • Trabeculated

    • Maybe some diverticula

  • Findinsg associated with preserving renal function & therefore better prognosis

    • Urinary ascites

    • Severe unilateral vesicoureteral reflux

    • Urinoma

    • Large bladder diverticula

    • These all basically act to relieve high pressure within the bladder

    • Basically these are all protective features

  • Treated surgically

Anterior Urethral Valves

  • Basically same as posterior urethral valves but located within the distal urethra (like in the shaft of the penis)

  • Will have a diverticula

  • Will have irregular bladder and dilated urethra proximal to the valve

Prune Belly Syndrome (Eagle-Barrett Syndrome)

  • Findings

    • Hydroureteronephrosis

    • Cryptorchidism

    • Abdominal wall laxity

References:

  • Case courtesy of Henry Knipe, Radiopaedia.org, rID: 41934