Human Reproduction, Vol. 17, No. 9, 2459-2463,
September 2002
© 2002 European Society of Human Reproduction and Embryology
Complete hydatidiform mole and normal live birth: a novel case of confined placental mosaicism: Case report
1 Departments of Obstetrics and Gynaecology and 2 Pathology, Ioannina University Hospital, Ioannina, Greece and 3 Trophoblastic Screening and Treatment Centre, Charing Cross Hospital, London, UK
Hydatidiform molar change, characterized by abnormal fetoplacental development and placental villous trophoblast hyperplasia, results from genetically abnormal conception, in which there is an excess of paternally derived genetic material. The majority of pregnancies in which molar change has been reported in association with a live fetus represent dizygotic twin pregnancies in which one fertilization results in a complete hydatidiform mole (CM) and the other a normal co-twin. In such cases, there is usually a clear distinction, both sonographically and pathologically, between the molar and non-molar regions of the placenta. We present a singleton pregnancy, with diffuse placental molar change detected prenatally, which resulted in a chromosomally and phenotypically normal female infant at term. Pathological examination revealed the presence of intermixed populations of morphologically normal chorionic villi and villi with the characteristics of CM. Studies of genetic polymorphisms demonstrated that the CM, normal villi and fetus were all derived from the same sperm; the fetus was diploid and biparental whereas the areas of pathological CM were androgenetic and monospermic. We believe this represents the first well-documented case of apparent confined placental mosaicism involving CM and a coexisting normal fetus, which has presumably arisen following mitotic abnormalities in the early post-fertilization period.
Key words: androgenetic/complete hydatidiform mole/monospermic/live birth/placental mosaicism
4 To whom correspondence should be addressed at: Trophoblastic Screening and Treatment Centre, Faculty of Medicine, Imperial College, Charing Cross Hospital, Fulham Palace Road, London, W6 8RF, UK. E-mail: r.fisher{at}ic.ac.uk
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
C. Deveault, J. H. Qian, W. Chebaro, A. Ao, L. Gilbert, A. Mehio, R. Khan, S. L. Tan, A. Wischmeijer, P. Coullin, et al. NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation Hum. Mol. Genet., March 1, 2009; 18(5): 888 - 897. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-C. Hsu, I-W. Lee, M.-T. Su, Y.-C. Lin, C. Hsieh, P.-Y. Chen, H.-W. Tsai, and P.-L. Kuo Triple genetic identities for the complete hydatidiform mole, placenta and co-existing fetus after transfer of a single in vitro fertilized oocyte: Case report and possible mechanisms Hum. Reprod., December 1, 2008; 23(12): 2686 - 2691. [Abstract] [Full Text] [PDF] |
||||
![]() |
D Kotzot Complex and segmental uniparental disomy updated J. Med. Genet., September 1, 2008; 45(9): 545 - 556. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. P. Robinson, J. L. Lauzon, A.M. Innes, K. Lim, S. Arsovska, and D. E. McFadden Origin and outcome of pregnancies affected by androgenetic/biparental chimerism Hum. Reprod., April 1, 2007; 22(4): 1114 - 1122. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Golubovsky Mosaic/chimeras and twinning in the current reproductive genetics perspective Hum. Reprod., September 1, 2006; 21(9): 2458 - 2460. [Full Text] [PDF] |
||||
![]() |
I Giurgea, D Sanlaville, J-C Fournet, C Sempoux, C Bellanne-Chantelot, G Touati, L Hubert, M-S Groos, F Brunelle, J Rahier, et al. Congenital hyperinsulinism and mosaic abnormalities of the ploidy J. Med. Genet., March 1, 2006; 43(3): 248 - 254. [Abstract] [Full Text] [PDF] |
||||
![]() |
K A Kaiser-Rogers, D E McFadden, C A Livasy, J Dansereau, R Jiang, J F Knops, L Lefebvre, K W Rao, and W P Robinson Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia J. Med. Genet., February 1, 2006; 43(2): 187 - 192. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Lucifero, J.R. Chaillet, and J. M. Trasler Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology Hum. Reprod. Update, January 1, 2004; 10(1): 3 - 18. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.D. Golubovsky Postzygotic diploidization of triploids as a source of unusual cases of mosaicism, chimerism and twinning Hum. Reprod., February 1, 2003; 18(2): 236 - 242. [Abstract] [Full Text] [PDF] |
||||



