Placental mesenchymal dysplasia: a case of a normal-appearing fetus with intrauterine growth restriction.

In this paper, we described a placenta with vesicular lesions in a 23-year-old woman (1-gravid) who visited our hospital at 13 weeks of gestation on prenatal routine examination. Ultrasound findings showed multiple vesicular lesions which gradually increased as the pregnancy advanced, and a live normal-appearing fetus which was confirmed of IUGR at 30 weeks of gestation in her uterus. Throughout gestation, the maternal serum β-human chorionic gonadotropin level keeps normal, but the serum alpha-fetoprotein was higher than average. The patient delivered an 1800-g female without obvious anomalies at 35 weeks 5 days of gestation due to premature rupture of membrane. The diagnosis of placental mesenchymal dysplasia was determined on the pathological examination and androgenetic/biparental mosaicism in the placenta was identified by immunohistochemical staining of p57kip2.

[1]  W. Wenbo,et al.  Pregnancy with Concomitant Chorioangioma and Placental Mesenchymal Dysplasia: A Rare Placental Abnormality , 2013, Case reports in obstetrics and gynecology.

[2]  T. Shiozawa,et al.  Placental Mesenchymal Dysplasia: Chronological Observation of Placental Images during Gestation and Review of the Literature , 2013, Gynecologic and Obstetric Investigation.

[3]  R. Kapur,et al.  Placental Mesenchymal Dysplasia. , 2013, Surgical pathology clinics.

[4]  T. Shirogane,et al.  Placental mesenchymal dysplasia, a case of intrauterine sudden death of fetus with rupture of cirsoid periumbilical chorionic vessels , 2011, Diagnostic pathology.

[5]  A. Heazell,et al.  A case of intrauterine growth restriction in association with placental mesenchymal dysplasia with abnormal placental lymphatic development. , 2009, Placenta.

[6]  S. Hassan,et al.  Three‐Dimensional Sonography of Placental Mesenchymal Dysplasia and Its Differential Diagnosis , 2009, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

[7]  D. Ang,et al.  Placental mesenchymal dysplasia: a potential misdiagnosed entity , 2009, Archives of Gynecology and Obstetrics.

[8]  Z. Parveen,et al.  Placental mesenchymal dysplasia. , 2007, Archives of pathology & laboratory medicine.

[9]  K. Benirschke,et al.  Placental Mesenchymal Dysplasia Is Associated With High Rates of Intrauterine Growth Restriction and Fetal Demise , 2006 .

[10]  C. Livasy,et al.  Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia , 2005, Journal of Medical Genetics.

[11]  Y. Kuwabara,et al.  Mesenchymal Stem Villous Hyperplasia of the Placenta and Fetal Growth Restriction , 2001, Obstetrics and gynecology.

[12]  N. Sebire,et al.  Pseudo‐partial moles: placental stem vessel hydrops and the association with Beckwith–Wiedemann syndrome and complete moles , 2001, Histopathology.

[13]  J. Lage Placentomegaly with massive hydrops of placental stem villi, diploid DNA content, and fetal omphaloceles: possible association with Beckwith-Wiedemann syndrome. , 1991, Human pathology.

[14]  J. Hustin,et al.  Placental vascular anomaly with diffuse mesenchymal stem villous hyperplasia. A new clinico-pathological entity? , 1991, Pathology, research and practice.