Placental Mesenchymal Dysplasia – a case report
Placental mesenchymal dysplasia (PMD) is a very rare vascular placenta anomaly, characterized by an enlarged placenta with grape-like vesicles. Initially, the disease can be mistaken for a molar pregnancy on ultrasound, but the condition is not a trophoblastic disorder, and presents with unique diagnostic and clinical features. Genetically, there is an association with androgenic/biparental mosaicism which can be confined to the placenta but also can be present in the fetus, and there is an increased risk of imprinting disorders such as Beckwith-Wiedemann syndrome. Obstetrically, PMD is associated with fetal growth restriction, preeclampsia, preterm delivery, and increased risk of intrauterine fetal demise. Thus, PMD is often associated with severe maternal and/or fetal complications, and this case illustrates the challenge in the diagnosis and prenatal counseling.
Authors
- Christian Beltoft Brøchner (ORCID: https://orcid.org/0000-0001-6838-6729)
- Adna Mohamud (ORCID: https://orcid.org/0000-0002-0239-1450)
- Tina Duelund Hjortshøj
- Louise Stig Hornstrup
Institutions
- Copenhagen University Hospital (DK)
- Gentofte Hospital (DK)
- Rigshospitalet (DK)
- Zealand University Hospital (DK)
Publication Details
- Journal
- Danish Journal of Obstetrics and Gynaecology
- Published
- 2025-01-22
- DOI
- https://doi.org/10.56182/c4h8g318
- Primary Topic
- Gestational Trophoblastic Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00