Pregnancy with Concomitant Chorioangioma and Placental Mesenchymal Dysplasia: A Rare Placental Abnormality

Background. Pregnancy with concomitant chorioangioma and placental mesenchymal dysplasia (PMD) coexisting with a normal viable fetus is very rare. The literature was reviewed to explore the incidence and genetic origin of this condition. Case. The case was first identified by prenatal ultrasonograph...

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Main Authors: Wu Qichang (Author), Wang Wenbo (Author), Zheng Liangkai (Author), Kong Hui (Author), He Xiaoqin (Author), Sun Li (Author), Xu Yasong (Author)
Format: Book
Published: Hindawi Limited, 2013-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Wu Qichang  |e author 
700 1 0 |a Wang Wenbo  |e author 
700 1 0 |a Zheng Liangkai  |e author 
700 1 0 |a Kong Hui  |e author 
700 1 0 |a He Xiaoqin  |e author 
700 1 0 |a Sun Li  |e author 
700 1 0 |a Xu Yasong  |e author 
245 0 0 |a Pregnancy with Concomitant Chorioangioma and Placental Mesenchymal Dysplasia: A Rare Placental Abnormality 
260 |b Hindawi Limited,   |c 2013-01-01T00:00:00Z. 
500 |a 2090-6684 
500 |a 2090-6692 
500 |a 10.1155/2013/591956 
520 |a Background. Pregnancy with concomitant chorioangioma and placental mesenchymal dysplasia (PMD) coexisting with a normal viable fetus is very rare. The literature was reviewed to explore the incidence and genetic origin of this condition. Case. The case was first identified by prenatal ultrasonography, but the prenatal diagnosis only included chorioangioma. PMD was then confirmed during postnatal evaluation, which included gross and histologic examination of the placenta. The macroscopic and microscopic findings were consistent with concomitant chorioangioma and placental mesenchymal dysplasia during pregnancy. Genetic findings confirmed genetic similarity of the chorioangioma and vesicle-like villi with the fetus. Conclusions. The case represents a rare placental abnormality whose pathogenesis and molecular basis need further research. Detailed histologic and genetic analyses are essential for accurate and differential diagnosis. 
546 |a EN 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n Case Reports in Obstetrics and Gynecology, Vol 2013 (2013) 
787 0 |n http://dx.doi.org/10.1155/2013/591956 
787 0 |n https://doaj.org/toc/2090-6684 
787 0 |n https://doaj.org/toc/2090-6692 
856 4 1 |u https://doaj.org/article/65793f9f920a4920a40c9ff9d2929f3b  |z Connect to this object online.