The article describes two Chinese boys ages 2 and 3 years with unilate
ral Wilms' tumors complicated by intracaval and intracardiac extension
. In contrast to the previously recommended treatment with surgery fol
lowed by chemotherapy and radiation therapy, the children were managed
primarily with combination chemotherapy before definitive operation.
Reduction of tumor size on serial imaging was documented, and no viabl
e tumor cells were found when the involved kidney and right atrium wer
e explored. Both patients remained alive without evidence of disease m
ore than 5 years after initial diagnosis. A literature search revealed
case reports and retrospective analyses of 70 patients with Wilms' tu
mors and intracardiac involvement, and a tendency toward preoperative
chemotherapy with or without the addition of radiation therapy was obs
erved. The overall outcome of this group of patients parallels the out
come of those without intracardiac extension by histology and stage. W
ilms' tumor presenting with extension into the inferior vena cava and
right atrium is thus rare and renders the affected child with addition
al cardiovascular complications and operative risks. As a result of th
e uncommon occurrence, a consensus on management based on prospective
study would be difficult. The present report and the literature are su
pportive of the use of preoperative chemotherapy in the initial manage
ment of advanced Wilms' tumor extending into the right atrium.