Gestational choriocarcinoma of the ovary is a rare form of malignancy
which can be difficult to distinguish from primary ovarian choriocarci
noma. The ability to make such a diagnosis could, however, have import
ant implications for therapy. We report here a case of choriocarcinoma
whose origins were difficult to determine and which behaved clinicall
y more like a primary rather than a gestational choriocarcinoma. We ha
ve analysed DNA from this tumour by using polymerase chain reaction (P
CR) amplification of a range of polymorphic alleles and have demonstra
ted that the tumour was in fact gestational. Furthermore, the lack of
chromosome Y sequences and the presence of heterozygosity of the spous
e's alleles, indicated that this tumour arose as a result of dispermic
fertilisation of an empty ovum by sperm carrying the X chromosome.