Over the last ten years 62 children were operated for renal tumours. T
he therapeutic aim in Wilms' tumours is complete macroscopic resection
of the primary tumour, assessing resectability as accurately as possi
ble. Overestimating surgical possibilities may lead to intraoperative
rupture of the tumour (three cases), while overestimating local tumour
extent may result in too much preoperative chemotherapy, which result
ed in the life-threatening complication of venous occlusive disease of
the hepatic veins (VOD) in three infants. The assessment of resectabi
lity may become particularly problematic in bilateral (six cases) or m
ultifocal Wilms' tumours (two cases), and in nephroblastomatosis (two
cases), i.e. the persistence of embronal renal tissue, a facultatively
precancerous lesion, which requires quarterly sonographic controls an
d which induced a second metachronous contralateral Wilms' tumour in o
ne child.