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Review Article| Volume 47, ISSUE 1, P29-48, March 2020

What Obstetricians Need to Know About Placental Pathology

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      References

      1. Khong T.Y. Mooney E.E. Nikkels P.G.J. Pathology of placenta: a practical guide. Springer, Cham (Switzerland)2019
      2. Redline R.W. Boyd T.K. Roberts D.J. Placental and gestational pathology. Cambridge University Press, Cambridge (United Kingdom)2018
        • Langston C.
        • Kaplan C.
        • Macpherson T.
        • et al.
        Practice guidelines for examination of the placenta. Developed by the placental pathology practice guideline development task force of the College of American Pathologists.
        Arch Pathol Lab Med. 1997; 121: 449-476
        • Cox P.
        • Evans C.
        Tissue pathway for histopathological examination of the placenta.
        The Royal College of Pathologists, London2017 (Available at:)
        • Baergen R.N.
        Indications for submission and macroscopic examination of the placenta.
        APMIS. 2018; 126: 544-550
        • Kaplan C.
        Umbilical cord.
        in: Color atlas of gross placental pathology. 2nd edition. Springer, New York2007: 25-44
        • Mills J.L.
        • Harley E.E.
        • Moessinger A.C.
        Standards for measuring umbilical cord length.
        Placenta. 1983; 4: 423-426
        • Georgiadis L.
        • Keski-Nisula L.
        • Harju M.
        • et al.
        Umbilical cord length in singleton gestations: a Finnish population-based retrospective register study.
        Placenta. 2014; 35: 275-280
        • Linde L.E.
        • Rasmussen S.
        • Kessler J.
        • et al.
        Extreme umbilical cord lengths, cord knot and entanglement: risk factors and risk of adverse outcomes, a population-based study.
        PLoS One. 2018; 13: e0194814
        • Ukazu A.
        • Ravikumar S.
        • Roche N.
        • et al.
        Are short umbilical cords seen in pathology really short?.
        Fetal Pediatr Pathol. 2018; 37: 359-362
        • Khong Y.T.
        • Mooney E.E.
        • Ariel I.
        • et al.
        Sampling and definitions of placental lesions: Amsterdam placental working group consensus statement.
        Arch Pathol Lab Med. 2016; 140: 698-713
        • Benton S.J.
        • Lafreniere A.J.
        • Grynspan D.
        • et al.
        A synoptic framework and future directions for placental pathology reporting.
        Placenta. 2019; 77: 46-57
        • Turowski G.
        • Parks W.T.
        • Arbuckle S.
        • et al.
        The structure and utility of the placental pathology report.
        APMIS. 2018; 126: 638-646
        • Redline R.W.
        Maternal vascular malperfusion.
        in: Redline R.W. Boyd T.K. Roberts D.J. Placental and gestational pathology. Cambridge University Press, Cambridge (United Kingdom)2018: 62-69
        • Redline R.W.
        Maternal vascular/trophoblastic developmental abnormalities.
        in: Redline R.W. Boyd T.K. Roberts D.J. Placental and gestational pathology. Cambridge University Press, Cambridge (United Kingdom)2018: 49-57
        • Redline R.W.
        • Ravishankar S.
        Fetal vascular malperfusion, an update.
        APMIS. 2018; 126: 561-569
        • Vik T.
        • Redline R.
        • Nelson K.B.
        • et al.
        The placenta in neonatal encephalopathy: a case-control study.
        J Pediatr. 2018; 202: 77-85
        • Redline R.W.
        • Pappin A.
        Fetal thrombotic vasculopathy: the clinical significance of extensive avascular villi.
        Hum Pathol. 1995; 26: 80-85
        • Redline R.W.
        Clinical and pathological umbilical cord abnormalities in fetal thrombotic vasculopathy.
        Hum Pathol. 2004; 35: 1494-1498
        • Parast M.M.
        • Crum C.P.
        • Boyd T.K.
        Placental histologic criteria for umbilical blood flow restriction in unexplained stillbirth.
        Hum Pathol. 2008; 39: 948-953
        • Saleemuddin A.
        • Tantbirojin P.
        • Sirois K.
        • et al.
        Obstetric and perinatal complications in placentas with fetal thrombotic vasculopathy.
        Pediatr Dev Pathol. 2010; 13: 459-464
        • Redline R.W.
        Severe fetal placental vascular lesions in term infants with neurologic impairment.
        Am J Obstet Gynecol. 2005; 192: 452-457
        • Redline R.W.
        • O’Riordan M.A.
        Placental lesions associated with cerebral palsy and neurologic impairment following term birth.
        Arch Pathol Lab Med. 2000; 124: 1785-1791
        • Vern T.Z.
        • Alles A.J.
        • Kowal Vern A.
        • et al.
        Frequency of factor V-Leiden and prothrombin G20210A in placentas and their relationship with placental lesions.
        Hum Pathol. 2000; 31: 1036-1043
        • Roberts D.
        Placental infections.
        in: Redline R.W. Boyd T.K. Roberts D.J. Placental and gestational pathology. Cambridge University Press, Cambridge (United Kingdom)2018: 115-136
        • Cox P.
        • Cohen M.C.
        • Scheimberg I.B.
        Acute chorioamnionitis.
        in: Khong T.Y. Mooney E.E. Nikkels P.G.J. Pathology of placenta: a practical guide. Springer, Cham (Switzerland)2019: 103-107
        • Redline R.W.
        • Faye-Petersen O.
        • Heller D.
        • et al.
        Amniotic infection syndrome: nosology and reproducibility of placental reaction patterns.
        Pediatr Dev Pathol. 2003; 6: 435-448
        • Ji H.
        • Bridges M.
        • Pesek E.
        • et al.
        Acute funisitis correlates with the risk of early-onset sepsis in term newborns assessed using the Kaiser Sepsis Calculator.
        Pediatr Dev Pathol. 2019; https://doi.org/10.1177/1093526619855467
        • Chisholm K.
        • Heerema-McKenney A.
        • Tian L.
        • et al.
        Correlation of preterm infant illness severity with placental histology.
        Placenta. 2016; 39: 61-69
        • Nath C.A.
        • Ananth C.V.
        • Smulian J.C.
        • et al.
        Histologic evidence of inflammation and risk of placental abruption.
        Am J Obstet Gynecol. 2007; 197: 319.e1-6
        • DeNoble A.E.
        • Heine R.P.
        • Dotters-Katz S.K.
        Chorioamnionitis and infectious complications after vaginal delivery.
        AM J Perinatol. 2019; https://doi.org/10.1055/s-0039-1692718
        • Redline R.W.
        Villitis of unknown etiology: noninfectious chronic villitis in the placenta.
        Hum Pathol. 2007; 38: 1439-1446
        • Parast M.
        Chronic villitis/villitis of unknown etiology.
        in: Redline R.W. Boyd T.K. Roberts D.J. Placental and gestational pathology. Cambridge University Press, Cambridge (United Kingdom)2018: 137-144
        • Heerema-McKenney A.
        Defense and infection of the human placenta.
        APMIS. 2018; 126: 570-588
        • Garcia A.G.
        • Fonseca E.F.
        • Marques R.L.
        • et al.
        Placental morphology in cytomegalovirus infection.
        Placenta. 1989; 10: 1-18
        • Sheffield J.S.
        • Sanchez P.J.
        • Wendel Jr., G.D.
        • et al.
        Placental histopathology of congenital syphilis.
        Obstet Gynecol. 2002; 100: 126-133
        • Rosenberg A.Z.
        • Yu W.
        • Hill D.A.
        • et al.
        Placental pathology of Zika virus: viral infection of the placenta induces villous stromal macrophage (Hofbauer cell) proliferation and hyperplasia.
        Arch Pathol Lab Med. 2017; 141: 43-48
        • Schwartz D.A.
        Viral infection, proliferation, and hyperplasia of Hofbauer cells and absence of inflammation characterize the placental pathology of fetuses with congenital Zika virus infection.
        Arch Gynecol Obstet. 2017; 295: 1361-1368
        • Katzman P.J.
        • Genest D.R.
        Maternal floor infarction and massive perivillous fibrin deposition: histological definitions, association with intrauterine fetal growth restriction, and risk of recurrence.
        Pediatr Dev Pathol. 2002; 5: 159-164
        • Katzman P.J.
        • Ernst L.M.
        • Scheimberg I.B.
        Massive perivillous fibrinoid deposition and maternal floor infarct.
        in: Khong T.Y. Mooney E.E. Nikkels P.G.J. Pathology of the placenta: a practical guide. Springer, Cham (Switzerland)2019: 77-82
        • Griffin A.C.
        • Strauss A.W.
        • Bennett M.J.
        • et al.
        Mutations in long-chain 3-hydroxyacyl coenzyme A dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition.
        Pediatr Dev Pathol. 2012; 15: 368-374
        • Abdulghani S.
        • Moretti F.
        • Gruslin A.
        • et al.
        Recurrent massive perivillous fibrin deposition and chronic intervillositis treated with heparin and intravenous immunoglobulin: a case report.
        J Obstet Gynaecol Can. 2017; 39: 676-681
        • Redline R.W.
        Chronic histiocytic intervillositis.
        in: Redline R.W. Boyd T.K. Roberts D.J. Placental and gestational pathology. Cambridge University Press, Cambridge (United Kingdom)2018: 152-155
        • Dubruc E.
        • Lebreton F.
        • Giannoli C.
        • et al.
        Placental histological lesions in fetal and neonatal alloimmune thrombocytopenia: a retrospective cohort study of 21 cases.
        Placenta. 2016; 48: 104-109
        • Marchaudon V.
        • Devisme L.
        • Petit S.
        • et al.
        Chronic histiocytic intervillositis of unknown etiology: clinical features in a consecutive series of 69 cases.
        Placenta. 2010; 32: 140-145
        • Mekinian A.
        • Costedoat-Chalumeau N.
        • Masseau A.
        • et al.
        Chronic histiocytic intervillositis: outcome, associated diseases and treatment in a multicenter prospective study.
        Autoimmunity. 2015; 48: 40-45