The presence of intratumoural heterogeneity in DNA distribution patter
ns has been accepted. However, most previous studies have not taken th
is fact into consideration. The value of DNA cytometry depends on its
reproducibility. This could be influenced by heterogeneity failure. Th
e aim of the present study is to evaluate intratumoural heterogeneity
in renal cell cancer. A sample of 22 tumours of the kidney was investi
gated by means of static DNA cytometry: 21 tumours were carcinomas, on
e was an angiomyolipoma. Probes from seven different locations of each
tumour were Feulgen-stained and measured. The variability of DNA feat
ures was determined and correlated with histological grade and type an
d with tumour size. There was considerable intratumoural heterogeneity
with respect to DNA distribution pattern in 45% of the tumours. Addit
ional non-diploid tumour-stemlines and deviation of computed DNA featu
res could be found in several cases by measuring more than one slide p
er tumour. A correlation between tumour heterogeneity, grading or typi
ng, and tumour size could not be found. Because these DNA parameters c
ould serve as the foundation of a risk-adapted treatment, tumour heter
ogeneity could have clinical consequences. Based on the results of thi
s study we suggest measuring at least three slides per tumour to avoid
misinterpretation of DNA measurements in renal cell cancer.