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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