Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series.

fetal demise fetal growth restriction hypertensive disorder of pregnancy maternal serum alpha-fetoprotein levels placental mesenchymal dysplasia

Journal

The journal of obstetrics and gynaecology research
ISSN: 1447-0756
Titre abrégé: J Obstet Gynaecol Res
Pays: Australia
ID NLM: 9612761

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 06 11 2020
revised: 15 12 2020
accepted: 22 12 2020
pubmed: 20 1 2021
medline: 22 6 2021
entrez: 19 1 2021
Statut: ppublish

Résumé

This study aimed to evaluate the clinical features and pregnancy outcomes of placental mesenchymal dysplasia (PMD) in Japan. We requested detailed clinical information and placental tissue of PMD cases in 2000-2018 from Japanese facilities with departments of obstetrics and gynecology and analyzed the pregnancy course and neonatal outcomes. We collected 49 cases of PMD. Of 18 patients with measured maternal serum alpha-fetoprotein (MSAFP) levels, 15 (83.3%) had elevated levels. Maternal serum human chorionic gonadotropin (MShCG) levels were transiently elevated in five (17.8%) of 28 patients. Forty-seven patients continued their pregnancies. All pregnancies were singleton and 40 (85.1%) were associated with adverse events including fetal growth restriction (FGR), threatened premature delivery, fetal demise, and hypertensive disorder of pregnancy in 34 (72.3%), 14 (29.8%), eight (17.0%), and six (12.8%) patients, respectively. Of 47 infants, there were eight stillbirths. There were 40 (85.1%) female infants, and eight (17.0%) had Beckwith-Wiedemann syndrome. Of 39 live births, 23 (59.0%) were associated with premature induction of labor or cesarean section for obstetric indications related to FGR. Eighteen (46.2%) neonates had complications. PMD-affected placentas were pathologically heterogeneous in both grossly PMD-affected and non-affected areas. Our study included the largest number of PMD cases with detailed clinical information. PMD is a high-risk condition for both the mother and the child. Elevated MSAFP levels with normal MShCG levels indicate PMD. Conventional perinatal management of FGR in Japan might be effective in reducing the fetal mortality rate.

Identifiants

pubmed: 33462953
doi: 10.1111/jog.14647
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1118-1125

Subventions

Organisme : a grant for research on intractable diseases from the Ministry of Health, Labour and Welfare of Japan
ID : H24-Nanchi-Ippan-077
Organisme : Japan Society for the Promotion of Science
ID : JP15K10678

Informations de copyright

© 2021 Japan Society of Obstetrics and Gynecology.

Références

Arisawa M, Nakayama M. Suspected involvement of the X chromosome in placental mesenchymal dysplasia. Cong Anomal 2002; 42: 309-317.
Takayama M, Soma H, Yaguchi S et al. Abnormally large placenta associated with Beckwith-Wiedemann syndrome. Gynecol Obstet Invest 1986; 22: 165-168.
Moscoso G, Jauniaux E, Hustin J. Placenta vascular anomaly with diffuse mesenchymal stem villous hyperplasia. A new clinic-pathological entity? Pathol Res Pract 1991; 187: 324-328.
Ohyama M, Kojyo T, Gotoda H, Sato T, Ijiri R, Tanaka Y. Mesenchymal dysplasia of the placenta. Pathol Int 2000; 50: 759-764.
Pham T, Steele J, Stayboldt C, Chan L, Benirschke K. Placental mesenchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise: A report of 11 new cases and a review of the literature. Am J Clin Pathol 2006; 126: 67-78.
Nayeri UA, West AB, Grossetta Nardini HK, Copel JA, Sfakianaki AK. Systematic review of sonographic findings of placental mesenchymal dysplasia and subsequent pregnancy outcome. Ultrasound Obstet Gynecol 2013; 41: 366-374.
Habib ZA. Maternal serum alpha-feto-protein: Its value in antenatal diagnosis of genetic disease and in obstetrical-gynaecological care. Acta Obstet Gynecol Scand Suppl 1977; 61: 1-92.
Gersell DJ, Kraus FT. Disease of the placenta. In: Kurman RJ, Ellenson LH, Ronnett BM (eds). Blaustein's pathology of the female genital tract, 6th edn. New York: Springer, 2011; 975-1048.
Rohilla M, Siwatch S, Jain V, Nijhawan R. Placentomegaly and placental mesenchymal dysplasia. BMJ Case Rep 2012. https://doi.org/10.1136/bcr-2012-007777.
Parveen Z, Tongson-Ignacio JE, Fraser CR, Killeen JL, Thompson KS. Placental mesenchymal dysplasia. Arch Pathol Lab Med 2007; 131: 131-137.
Mulch AD, Stallings SP, Salafia CM. Elevated maternal serum alpha-fetoprotein, umbilical vein varix, and mesenchymal dysplasia: are they related? Prenat Diagn 2006; 26: 659-661.
Aviram R, Kidron D, Silverstein S et al. Placental mesenchymal dysplasia associated with transient neonatal diabetes mellitus and paternal UPD6. Placenta 2008; 29: 646-649.
Bogart MH, Pandian MR, Jones OW. Abnormal maternal serum chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities. Prenat Diagn 1987; 7: 623-630.
Walton DL, Norem CT, Schoen EJ, Ray GT, Colby CJ. Second-trimester serum chorionic gonadotropin concentrations and complications and outcome of pregnancy. N Engl J Med 1999; 341: 2033-2038.
Ishikawa S, Morikawa M, Umazume T et al. Anemia in a neonate with placental mesenchymal dysplasia. Clin Case Rep 2016; 4: 463-465.
Wangler MF, Chang AS, Moley KH, Feinberg AP, Debaun MR. Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registry. Am J Med Genet A 2005; 134: 187-191.
Higashimoto K, Soejima H, Saito T, Okumura K, Mukai T. Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer. Cytogenet Genome Res 2006; 113: 306-312.
Dokras A, Hoffmann DS, Eastvold JS et al. Severe feto-placental abnormalities precede the onset of hypertension and proteinuria in a mouse model of preeclampsia. Biol Reprod 2006; 75: 899-907.
Romanelli V, Belinchon A, Campos-Barros A et al. CDKN1C mutations in HELLP/ preeclamptic mothers of Beckwith-Wiedemann syndrome (BWS) patients. Placenta 2009; 30: 551-554.
Guenot C, Kingdaom J, Rham MD et al. Placental mesenchymal dysplasia: an underdiagnosed placental pathology with various clinical outcomes. Eur J Obstet Gynecol Reprod Biol 2019; 234: 155-164.
Jauniaux E, Nicolaides KH, Hustin J. Perinatal features associated with placental mesenchymal dysplasia. Placenta 1997; 18: 701-706.

Auteurs

Chisato Kodera (C)

Department of Obstetrics and Gynecology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

Saori Aoki (S)

Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga, Japan.

Takashi Ohba (T)

Department of Obstetrics and Gynecology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

Ken Higashimoto (K)

Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga, Japan.

Yoshiki Mikami (Y)

Department of Diagnostic Pathology, Kumamoto University Hospital, Kumamoto, Japan.

Masaharu Fukunaga (M)

Department of Pathology, Shin-Yurigaoka General Hospital, Kawasaki, Japan.

Hidenobu Soejima (H)

Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga, Japan.

Hidetaka Katabuchi (H)

Department of Obstetrics and Gynecology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

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