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placental mesenchymal dysplasia
Thursday 30 November 2006
Definition: Placental mesenchymal dysplasia is a rare human placental disorder in which the placenta is enlarged and contains cystic villi and dilated vasculature. In contrast to a partial mole, mesenchymal dysplasia may coexist with a normal fetus.
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Placental mesenchymal dysplasia
Synopsis
placenta enlarged with abnormal, large, and often cystic villi
placental dilated and/or thick-walled vessels
large, hydropic stem villi
myxomatous stroma
cistern formation
vascular proliferation / ’chorangiomatoid’ changes
Etiology
normal karyotype (89%) (15791673)
abnormal karyotype (11%) (15791673)
- trisomy 13
- Klinefelter syndrome (47,XXY)
- 69,XXX triploidy
Beckwith-Wiedemann syndrome (BWS) (23%) (15791673)
Differential diagnosis
partial hydatidiform mole
- In contrast to a partial mole, it can coexist with a fully viable fetus.
Associations
Fetal anatomical and vascular anomalies
- hepatic mesenchymal hamartoma (mesenchymal hamartoma of the liver) (17378624)
References
Francis B, Hallam L, Kecskes Z, Ellwood D, Croaker D, Kent A. Placental mesenchymal dysplasia associated with hepatic mesenchymal hamartoma in the newborn. Pediatr Dev Pathol. 2007 Jan-Feb;10(1):50-4. PMID: 17378624
Cohen MC, Roper EC, Sebire NJ, Stanek J, Anumba DO. Placental mesenchymal dysplasia associated with fetal aneuploidy. Prenat Diagn. 2005 Mar;25(3):187-92. PMID: 15791673