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Chapter 34 - Central Nervous System Injury

from Section 9 - Clinicopathologic Correlations: Placental Pathology and Adverse Pregnancy Outcomes

Published online by Cambridge University Press:  03 September 2018

Raymond W. Redline
Affiliation:
Case Western Reserve University, Ohio
Theonia K. Boyd
Affiliation:
Harvard Medical School, Boston
Drucilla J. Roberts
Affiliation:
Harvard Medical School, Boston
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Publisher: Cambridge University Press
Print publication year: 2017

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References

Mir, IN, Johnson-Welch, SF, Nelson, DB, et al. Placental pathology is associated with severity of neonatal encephalopathy and adverse developmental outcomes following hypothermia. Am J Obstet Gynecol. 2015;213:849 e17.Google Scholar
Spedding, M, Evrard, P, Gressens, P. Neuroprotection in the newborn infant: interactions between stress, glutamate, glucocorticoids and development. Dev Med Child Neurol Suppl. 2001;86:10–2.Google ScholarPubMed
Xing, C, Lo, EH. Help-me signaling: Non-cell autonomous mechanisms of neuroprotection and neurorecovery. Prog Neurobiol. 2017;152:181–99.Google Scholar
Volpe, JJ. Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances. Lancet Neurol. 2009;8:110–24.Google Scholar
Myers, RE. Four patterns of perinatal brain damage and their conditions of occurrence in primates. Adv Neurol. 1975;10:223–34.Google Scholar
MacLennan, A. A template for defining a causal relation between acute intrapartum events and cerebral palsy: international consensus statement. BMJ. 1999;319:1054–9.Google Scholar
Martinez-Biarge, M, Madero, R, Gonzalez, A, et al. Perinatal morbidity and risk of hypoxic-ischemic encephalopathy associated with intrapartum sentinel events. Am J Obstet Gynecol. 2012;206:148 e17.Google Scholar
Fleiss, B, Tann, CJ, Degos, V, et al. Inflammation-induced sensitization of the brain in term infants. Dev Med Child Neurol. 2015;57 Suppl 3:1728.Google Scholar
Redline, RW. Disorders of placental circulation and the fetal brain. Clin Perinatol. 2009;36:549–59.Google Scholar
Gustavsson, M, Anderson, MF, Mallard, C, et al. Hypoxic preconditioning confers long-term reduction of brain injury and improvement of neurological ability in immature rats. Pediatr Res. 2005;57:305–9.Google Scholar
Madsen-Bouterse, SA, Romero, R, Tarca, AL, et al. The transcriptome of the fetal inflammatory response syndrome. Am J Reprod Immunol. 2010;63:7392.Google Scholar
Kim, MJ, Romero, R, Kim, CJ, et al. Villitis of unknown etiology is associated with a distinct pattern of chemokine up-regulation in the feto-maternal and placental compartments: implications for conjoint maternal allograft rejection and maternal anti-fetal graft-versus-host disease. J Immunol. 2009;182:3919–27.Google Scholar
Challier, JC, Basu, S, Bintein, T, et al. Obesity in pregnancy stimulates macrophage accumulation and inflammation in the placenta. Placenta. 2008;29:274–81.Google Scholar
van der Burg, JW, Allred, EN, McElrath, TF, et al. Is maternal obesity associated with sustained inflammation in extremely low gestational age newborns? Early Hum Dev. 2013;89:949–55.CrossRefGoogle ScholarPubMed
investigators Den. The correlation between placental pathology and intraventricular hemorrhage in the preterm infant. Pediatr Res. 1998;43:15–9.Google Scholar
Bejar, R, Wozniak, P, Allard, M, et al. Antenatal origin of neurologic damage in newborn infants. I. Preterm infants. Am J Obstet Gynecol. 1988;159:357–63.Google Scholar
Polam, S, Koons, A, Anwar, M, et al. Effect of chorioamnionitis on neurodevelopmental outcome in preterm infants. Arch Pediatr Adolesc Med. 2005;159:1032–5.Google Scholar
Wu, YW, Colford, JM Jr. Chorioamnionitis as a risk factor for cerebral palsy: A meta-analysis. JAMA. 2000;284:1417–24.CrossRefGoogle ScholarPubMed
Lee, J, Croen, LA, Backstrand, KH, et al. Maternal and infant characteristics associated with perinatal arterial stroke in the infant. JAMA. 2005;293:723–9.CrossRefGoogle ScholarPubMed
DeFelice, C, Toti, P, Laurini, RN, et al. Early neonatal brain injury in histologic chorioamnionitis. J Pediatr. 2001;138:101–4.Google Scholar
Rovira, N, Alarcon, A, Iriondo, M, et al. Impact of histological chorioamnionitis, funisitis and clinical chorioamnionitis on neurodevelopmental outcome of preterm infants. Early Hum Dev. 2011;87:253–7.Google Scholar
Knuesel, I, Chicha, L, Britschgi, M, et al. Maternal immune activation and abnormal brain development across CNS disorders. Nat Rev Neurol. 2014;10:643–60.CrossRefGoogle ScholarPubMed
Kim, CJ, Yoon, BH, Romero, R, et al. Umbilical arteritis and phlebitis mark different stages of the fetal inflammatory response. Am J Obstet Gynecol. 2001;185:496500.Google Scholar
Rogers, BB, Alexander, JM, Head, J, et al. Umbilical vein interleukin-6 levels correlate with the severity of placental inflammation and gestational age. Hum Pathol. 2002;33:335–40.Google Scholar
Redline, RW, Wilson-Costello, D, Borawski, E, et al. Placental lesions associated with neurologic impairment and cerebral palsy in very low birth weight infants. Arch Pathol Lab Med. 1998;122:1091–8.Google Scholar
Redline, RW, O’Riordan, MA. Placental lesions associated with cerebral palsy and neurologic impairment following term birth. Arch Pathol Lab Med. 2000;124:1785–91.CrossRefGoogle ScholarPubMed
Redline, RW, Minich, N, Taylor, HG, et al. Placental lesions as predictors of cerebral palsy and abnormal neurocognitive function at school age in extremely low birth weight infants (< 1.0kg). Pediatr Dev Pathol. 2007;10:282–92.Google Scholar
Scher, MS, Trucco, GS, Beggarly, ME, et al. Neonates with electrically confirmed seizures and possible placental associations. Pediatr Neurol. 1998;19:3741.Google Scholar
Harteman, JC, Nikkels, PG, Benders, MJ, et al. Placental pathology in full-term infants with hypoxic-ischemic neonatal encephalopathy and association with magnetic resonance imaging pattern of brain injury. J Pediatr. 2013;163:968–95 e2.Google Scholar
Redline, RW. Cerebral palsy in term infants: a clinicopathologic analysis of 158 medicolegal case reviews. Pediatr Dev Pathol. 2008;11:456–64.Google Scholar
McDonald, DG, Kelehan, P, McMenamin, JB, et al. Placental fetal thrombotic vasculopathy is associated with neonatal encephalopathy. Hum Pathol. 2004;35:875–80.Google Scholar
Elbers, J, Viero, S, MacGregor, D, et al. Placental pathology in neonatal stroke. Pediatrics. 2011;127:e722–9.Google Scholar
Ko, HS, Cheon, JY, Choi, SK, et al. Placental histologic patterns and neonatal seizure, in preterm premature rupture of membrane. J Matern Fetal Neonatal Med. 2016:18.Google Scholar
Chang, KT, Keating, S, Costa, S, et al. Third-trimester stillbirths: correlative neuropathology and placental pathology. Pediatr Dev Pathol. 2011;14:345–52.Google Scholar
Grafe, MR. The correlation of prenatal brain damage with placental pathology. N Neuropathol Exp Neurol. 1994;53:407–15.Google Scholar
McElrath, TF, Allred, EN, Kuban, K, et al. Factors associated with small head circumference at birth among infants born before the 28th week. Am J Obstet Gynecol. 2010;203:138 e18.CrossRefGoogle ScholarPubMed
Burke, CJ, Tannenberg, AE. Prenatal brain damage and placental infarction: an autopsy study. Dev Med Child Neurol. 1995;37:555–62.Google Scholar
Blair, E, de Groot, J, Nelson, KB. Placental infarction identified by macroscopic examination and risk of cerebral palsy in infants at 35 weeks of gestational age and over. Am J Obstet Gynecol. 2011;205:124 e17.Google Scholar
Adams-Chapman, I, Vaucher, YE, Bejar, RF, et al. Maternal floor infarction of the placenta: association with central nervous system injury and adverse neurodevelopmental outcome. J Perinatol. 2002;22:236–41.Google Scholar
Higgins, M, McAuliffe, FM, Mooney, EE. Clinical associations with a placental diagnosis of delayed villous maturation: a retrospective study. Pediatr Dev Pathol. 2011;14:273–9.CrossRefGoogle ScholarPubMed
Naeye, RL, Maisels, J, Lorenz, RP, et al. The clinical significance of placental villous edema. Pediatrics. 1983;71:588–94.Google Scholar
Avagliano, L, Locatelli, A, Danti, L, et al. Placental histology in clinically unexpected severe fetal acidemia at term. Early Hum Dev. 2015;91:339–43.Google Scholar
Viscardi, RM, Sun, CC. Placental lesion multiplicity: risk factor for IUGR and neonatal cranial ultrasound abnormalities. Early Hum Dev. 2001;62:110.Google Scholar

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