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230<br />

ABDOMINAL ULTRASOUND<br />

LT<br />

LT<br />

A<br />

B<br />

Figure 9.11 (A) The dilated collecting system of this kidney is filled with a large, rounded fungal ball of candidiasis<br />

infection. (B) The fungus ball is seen to disintegrate, emptying into the renal pelvis.<br />

The tumours are large at presentation, presenting<br />

with a palpable abdominal mass, and, less frequently,<br />

pain, haematuria and fever. About 5% of these<br />

tumours are bilateral. 20 The prognosis when unilateral<br />

is generally good.<br />

The ultrasound appearances are of a relatively<br />

well-defined heterogeneous mass, predominantly<br />

solid but frequently with some necrotic or haemorrhagic<br />

areas, often almost completely replacing<br />

the kidney (Fig. 9.12). Small focal areas of calcification<br />

are seen very occasionally. A search should<br />

be made for tumour invasion of the renal vein and<br />

IVC which occurs in up to 10% of cases. Tumour<br />

invasion may extend into the right atrium.<br />

Occasionally a large, right-sided Wilms’ tumour<br />

may compress the IVC but not invade it; colour or<br />

power Doppler may be useful in the difficult distinction<br />

between compression and invasion on<br />

ultrasound. Ultrasound also identifies associated<br />

lymphadenopathy, particularly in the para-aortic<br />

and paracaval regions, and metastatic liver disease.<br />

In a small percentage of cases, tumour may also<br />

be found in the contralateral kidney. This is usually<br />

much smaller than the mass on the presenting side<br />

and may be acoustically subtle. Up to 7% of contralateral<br />

tumours are missed on preoperative<br />

imaging due to their small size and the operator<br />

must be alert to the possibility of bilateral disease. 20<br />

Occasionally a Wilms’ tumour may be found to<br />

be predominantly cystic, having the appearances of<br />

a large, multiloculated cystic mass. The main differential<br />

diagnosis would be of a mesonephric blastoma<br />

occurring during the first year of life and<br />

histology is required to establish the diagnosis.<br />

In most cases, an ultrasound and chest radiograph<br />

are sufficient to diagnose correctly Wilms’<br />

tumour but CT of the chest and abdomen is generally<br />

used for staging, and to exclude metastatic<br />

disease in the chest and liver. 21 Percutaneous<br />

biopsy for confirmation of histological type is generally<br />

performed. CT or MRI is more sensitive<br />

than ultrasound scanning in demonstrating small<br />

tumours in the contralateral kidney.<br />

Xanthogranulomatous pyelonephritis<br />

Xanthogranulomatous pyelonephritis results from<br />

chronic infection in an obstructed kidney and children<br />

present with a history of general malaise, lowgrade<br />

fever and flank pain and may be found to be<br />

anaemic. The finding of a palpable abdominal mass<br />

on examination often leads to an early diagnosis of<br />

a possible Wilms’ tumour. On sonography the kidney<br />

is diffusely enlarged, with loss of the normal<br />

corticomedullary differentiation. The presence of<br />

calyceal dilatation with debris and calculi in the collecting<br />

system and confirmation of urinary infection<br />

in addition to the generalized involvement of<br />

the kidney helps to differentiate this condition<br />

from Wilms’ tumour (Fig. 9.12B). Occasionally

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