The histogenesis of carcinosarcomas has intrigued pathologists for a l
ong time and remains unresolved. Two main theories have been put forwa
rd, one suggesting that they are monoclonal, another suggesting that t
hey are biclonal. Our study examined p53 immunostaining in 17 uterine
carcinosarcomas (mixed Mullerian tumours) and found positivity in five
(30%). There was no disparity in immunostaining between the epithelia
l and the stromal components in any of the 17 tumours. This concordanc
e in every tumour would be very unlikely if carcinosarcomas are biclon
al; However, it would be expected if carcinosarcomas are monoclonal.