PARTIAL HYDATID MOLE IN A CYTOGENETICALLY NORMAL FETUS

Citation
E. Beinder et al., PARTIAL HYDATID MOLE IN A CYTOGENETICALLY NORMAL FETUS, Geburtshilfe und Frauenheilkunde, 55(6), 1995, pp. 351-353
Citations number
8
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
00165751
Volume
55
Issue
6
Year of publication
1995
Pages
351 - 353
Database
ISI
SICI code
0016-5751(1995)55:6<351:PHMIAC>2.0.ZU;2-9
Abstract
The diagnosis of a partial hydatid mole presents a difficult situation for both physician and parents. On the one hand there may be a normal pregnancy whereas on the other hand the mother may be threatened by n umerous complications caused by the hydatid mole if the pregnancy is c ontinued. We report on a pregnancy in the 18th week during which a par tial hydatid mole was discovered where we considered it justified to a dvise the parents, after a thorough consultation, to continue with the pregnancy. Ultrasound examination had excluded infaust malformations whereas cytogenetically there was no triploidy of the fetus. Moreover it was possible to closely monitor the course of pregnancy to discover any possible complications well in time. Under these conditions conti nuation of pregnancy until birth is possible in about 60 % of the case s without enhanced risk to the mother, as is evident from the data in the literature. In the case under report, however there was a life-thr eatening uterine haemorrhage with placenta previa in the 22nd week of pregnancy resulting in mandatory premature termination of pregnancy. R epeated treatment with cytostatics was subsequently required due to pe rsistence of the mole, since even hysterectomy could not achieve compl ete remission of the disease.