Wilms tumour (nephroblastoma)

USG · CT · MRI

First and second year — the floor first, then every step

A large renal mass in a young child that arises from the kidney (claw sign), displaces rather than encases vessels, and may extend into the renal vein and IVC — report the contralateral kidney, the venous extent and the lungs.

Orient first

  • Peak age 3–4 years; bilateral in a minority (syndromes, nephroblastomatosis).
  • Wilms displaces vessels and crosses the midline less; neuroblastoma encases vessels, calcifies and lifts the aorta.
  • SIOP (pre-operative chemotherapy) and COG (upfront surgery) pathways differ (verify which applies).

Acquire the study

  • Curvilinear probe; colour Doppler of the renal vein and IVC.

The manoeuvre

  • Mass arising from the kidney: claw of normal parenchyma around it.
  • Size in cm in three planes; heterogeneity.
  • Renal vein and IVC: tumour thrombus and its upper extent on colour Doppler.
  • Contralateral kidney: a second lesion.

What confirms it

  • A renal-origin mass with typical features; histology after chemotherapy or surgery.

What licenses you to exclude it

  • Adrenal origin, vessel encasement and calcification favour neuroblastoma.

The classic misread

  • An adrenal neuroblastoma indenting the kidney mistaken for a renal mass.

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