Skip to main navigation menu Skip to main content Skip to site footer

Review article: Medical guidelines

Vol. 154 No. 10 (2024)

Pathologic findings of the placenta and clinical implications – recommendations for placental examination

DOI
https://doi.org/10.57187/s.3929
Cite this as:
Swiss Med Wkly. 2024;154:3929
Published
14.10.2024

Summary

The placenta is a unique and complex organ that combines the circulatory systems of two or more individuals within a single dynamic organ with a set, short lifespan. A diverse spectrum of disorders, including infections as well as metabolic, genetic, circulatory, and maturation defects, may affect its function. Pathology investigation of the placenta is key for identifying several pathogenic processes in both the mother and the foetus. Aberrant placentation, maternal and foetal vascular compromise, infection, inflammatory immunologic conditions, and disorders of maturation are elements of newly proposed classification schemes.

The clinical impact of placental examination consists of diagnosing maternal and foetal disease, identifying the potential for recurrence, correlating clinical pathological findings with distinct morphologic features, and identifying the aetiology responsible for growth restriction or foetal death.

Gestational trophoblastic disease occurs more frequently in the first trimester; however, in very rare cases, it can affect the term or third-trimester placenta.

The application of reproducible nomenclature is expected to facilitate progress in the diagnosis and treatment of obstetric and foetal disorders with placental manifestation.

Therefore, this review aims to facilitate communication between obstetricians, neonatologists, and pathologists involved in this diagnostic process.

References

  1. Langston C, Kaplan C, Macpherson T, Manci E, Peevy K, Clark B, et al. Practice guideline 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 May;121(5):449–76.
  2. Roberts DJ, Baergen RN, Boyd TK, Carreon CK, Duncan VE, Ernst LM, et al. Criteria for placental examination for obstetrical and neonatal providers. Am J Obstet Gynecol. 2023 May;228(5):497–508.e4. doi: https://doi.org/10.1016/j.ajog.2022.12.017 DOI: https://doi.org/10.1016/j.ajog.2022.12.017
  3. S2k-Leitlinie Pathomorphologische Untersuchung der Plazenta. 2022. AWMF Registriernummer 035/005. available from: https://register.awmf.org/de/leitlinien/detail/035-005
  4. Evans, C., et al., Tissue pathway for histological examination of the placenta. The Royal college of pathologists. G 108, 2022.
  5. Polnaszek BE, Clark SL, Rouse DJ. Pathologic Assessment of the Placenta: Evidence Compared With Tradition. Obstet Gynecol. 2022 Apr;139(4):660–7. doi: https://doi.org/10.1097/AOG.0000000000004719 DOI: https://doi.org/10.1097/AOG.0000000000004719
  6. Khong TY, Mooney EE, Ariel I, Balmus NC, Boyd TK, Brundler MA, et al. Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement. Arch Pathol Lab Med. 2016 Jul;140(7):698–713. doi: https://doi.org/10.5858/arpa.2015-0225-CC DOI: https://doi.org/10.5858/arpa.2015-0225-CC
  7. Slack JC, Parra-Herran C. Life After Amsterdam: Placental Pathology Consensus Recommendations and Beyond. Surg Pathol Clin. 2022 Jun;15(2):175–96. doi: https://doi.org/10.1016/j.path.2022.02.001 DOI: https://doi.org/10.1016/j.path.2022.02.001
  8. Zhou YY, Ravishankar S, Luo G, Redline RW. Predictors of High Grade and Other Clinically Significant Placental Findings by Indication for Submission in Singleton Placentas From Term Births. Pediatr Dev Pathol. 2020 Aug;23(4):274–84. doi: https://doi.org/10.1177/1093526620904801 DOI: https://doi.org/10.1177/1093526620904801
  9. Guttmacher AE, Maddox YT, Spong CY. The Human Placenta Project: placental structure, development, and function in real time. Placenta. 2014 May;35(5):303–4. doi: https://doi.org/10.1016/j.placenta.2014.02.012 DOI: https://doi.org/10.1016/j.placenta.2014.02.012
  10. Roberts JM, Hansson SR, Vaiman D, Redman CW; Global Pregnancy Collaboration. Global Pregnancy Collaboration symposium on placental health: summary and recommendations. Placenta. 2017 Apr;52:116–21. doi: https://doi.org/10.1016/j.placenta.2017.01.115 DOI: https://doi.org/10.1016/j.placenta.2017.01.115
  11. Odibo I, Gehlot A, Ounpraseuth ST, Magann EF. Pathologic examination of the placenta and its clinical utility: a survey of obstetrics and gynecology providers. J Matern Fetal Neonatal Med. 2016;29(2):197–201. doi: https://doi.org/10.3109/14767058.2014.998192 DOI: https://doi.org/10.3109/14767058.2014.998192
  12. Sebire NJ. Implications of placental pathology for disease mechanisms; methods, issues and future approaches. Placenta. 2017 Apr;52:122–6. doi: https://doi.org/10.1016/j.placenta.2016.05.006 DOI: https://doi.org/10.1016/j.placenta.2016.05.006
  13. Redline RW, Roberts DJ, Parast MM, Ernst LM, Morgan TK, Greene MF, et al. Placental pathology is necessary to understand common pregnancy complications and achieve an improved taxonomy of obstetrical disease. Am J Obstet Gynecol. 2023 Feb;228(2):187–202. doi: https://doi.org/10.1016/j.ajog.2022.08.010 DOI: https://doi.org/10.1016/j.ajog.2022.08.010
  14. Redline RW. The clinical implications of placental diagnoses. Semin Perinatol. 2015 Feb;39(1):2–8. doi: https://doi.org/10.1053/j.semperi.2014.10.002 DOI: https://doi.org/10.1053/j.semperi.2014.10.002
  15. Redline RW. Classification of placental lesions. Am J Obstet Gynecol. 2015 Oct;213(4 Suppl):S21–8. doi: https://doi.org/10.1016/j.ajog.2015.05.056 DOI: https://doi.org/10.1016/j.ajog.2015.05.056
  16. Gabriel H, Korinth D, Ritthaler M, Schulte B, Battke F, von Kaisenberg C, et al. Trio exome sequencing is highly relevant in prenatal diagnostics. Prenat Diagn. 2022 Jun;42(7):845–51. doi: https://doi.org/10.1002/pd.6081 DOI: https://doi.org/10.1002/pd.6081
  17. Redline RW. Placental pathology: is it time to get serious? Contemp Ob Gyn. 2014;59(2):41–8.
  18. Khong TY. Evidence-based pathology: umbilical cord coiling. Pathology. 2010 Dec;42(7):618–22. doi: https://doi.org/10.3109/00313025.2010.520309 DOI: https://doi.org/10.3109/00313025.2010.520309
  19. Cromb D, et al. Clinical value of placental examination for paediatricians. Arch Dis Child Fetal Neonatal Ed. 2023. DOI: https://doi.org/10.1136/archdischild-2023-325674
  20. de Laat MW, Franx A, van Alderen ED, Nikkels PG, Visser GH. The umbilical coiling index, a review of the literature. J Matern Fetal Neonatal Med. 2005 Feb;17(2):93–100. doi: https://doi.org/10.1080/jmf.17.2.93.100 DOI: https://doi.org/10.1080/14767050400028899
  21. Dirnhofer S, B.L., Lehr HA, Landau B, Zenklusen HR, Qualitätsrichtlinien SGPath. 2011.
  22. Avagliano L, Locatelli A, Danti L, Felis S, Mecacci F, Bulfamante GP. Placental histology in clinically unexpected severe fetal acidemia at term. Early Hum Dev. 2015 May;91(5):339–43. doi: https://doi.org/10.1016/j.earlhumdev.2015.03.004 DOI: https://doi.org/10.1016/j.earlhumdev.2015.03.004
  23. Chen A, Roberts DJ. Placental pathologic lesions with a significant recurrence risk - what not to miss! APMIS. 2018 Jul;126(7):589–601. doi: https://doi.org/10.1111/apm.12796 DOI: https://doi.org/10.1111/apm.12796
  24. Kaspar HG, Abu-Musa A, Hannoun A, Seoud M, Shammas M, Usta I, et al. The placenta in meconium staining: lesions and early neonatal outcome. Clin Exp Obstet Gynecol. 2000;27(1):63–6.
  25. Spong CY, Mercer BM, D’Alton M, Kilpatrick S, Blackwell S, Saade G. Timing of indicated late-preterm and early-term birth. Obstet Gynecol. 2011 Aug;118(2 Pt 1):323–33. doi: https://doi.org/10.1097/AOG.0b013e3182255999 DOI: https://doi.org/10.1097/AOG.0b013e3182255999
  26. Abdulghani S, Moretti F, Gruslin A, Grynspan D. Recurrent Massive Perivillous Fibrin Deposition and Chronic Intervillositis Treated With Heparin and Intravenous Immunoglobulin: A Case Report. J Obstet Gynaecol Can. 2017 Aug;39(8):676–81. doi: https://doi.org/10.1016/j.jogc.2017.03.089 DOI: https://doi.org/10.1016/j.jogc.2017.03.089
  27. Dubruc E, Lebreton F, Giannoli C, Rabilloud M, Huissoud C, Devouassoux-Shisheboran M, et al. Placental histological lesions in fetal and neonatal alloimmune thrombocytopenia: A retrospective cohort study of 21 cases. Placenta. 2016 Dec;48:104–9. doi: https://doi.org/10.1016/j.placenta.2016.10.009 DOI: https://doi.org/10.1016/j.placenta.2016.10.009
  28. Nedberg NH, Turowski G, Guz K, Przytuła E, Uhrynowska M, Roald B, et al. Platelet alloimmunization is associated with low grade chronic histiocytic intervillositis - A new link to a rare placental lesion? Placenta. 2021 Sep;112:89–96. doi: https://doi.org/10.1016/j.placenta.2021.07.291 DOI: https://doi.org/10.1016/j.placenta.2021.07.291
  29. Romero R, Whitten A, Korzeniewski SJ, Than NG, Chaemsaithong P, Miranda J, et al. Maternal floor infarction/massive perivillous fibrin deposition: a manifestation of maternal antifetal rejection? Am J Reprod Immunol. 2013 Oct;70(4):285–98. doi: https://doi.org/10.1111/aji.12143 DOI: https://doi.org/10.1111/aji.12143
  30. Redline RW. Severe fetal placental vascular lesions in term infants with neurologic impairment. Am J Obstet Gynecol. 2005 Feb;192(2):452–7. doi: https://doi.org/10.1016/j.ajog.2004.07.030 DOI: https://doi.org/10.1016/j.ajog.2004.07.030
  31. Hösli I, et al. Gestationsdiabetes. Schweiz Arzteztg. 2023;103(38):88–90. DOI: https://doi.org/10.4414/saez.2023.22112
  32. Redline RW. Disorders of placental circulation and the fetal brain. Clin Perinatol. 2009 Sep;36(3):549–59. doi: https://doi.org/10.1016/j.clp.2009.06.003 DOI: https://doi.org/10.1016/j.clp.2009.06.003
  33. Clapp JF 3rd, Lopez B, Simonean S. Nuchal cord and neurodevelopmental performance at 1 year. J Soc Gynecol Investig. 1999;6(5):268–72. DOI: https://doi.org/10.1016/S1071-5576(99)00020-9
  34. Myers RE. Fetal asphyxia due to umbilical cord compression. Metabolic and brain pathologic consequences. Biol Neonate. 1975;26(1-2):21–43. doi: https://doi.org/10.1159/000240714 DOI: https://doi.org/10.1159/000240714
  35. Guzick DS, Winn K. The association of chorioamnionitis with preterm delivery. Obstet Gynecol. 1985 Jan;65(1):11–6.
  36. Redline RW. Inflammatory response in acute chorioamnionitis. Semin Fetal Neonatal Med. 2012 Feb;17(1):20–5. doi: https://doi.org/10.1016/j.siny.2011.08.003 DOI: https://doi.org/10.1016/j.siny.2011.08.003
  37. Leviton A, Allred EN, Kuban KC, Hecht JL, Onderdonk AB, O’shea TM, et al. Microbiologic and histologic characteristics of the extremely preterm infant’s placenta predict white matter damage and later cerebral palsy. the ELGAN study. Pediatr Res. 2010 Jan;67(1):95–101. doi: https://doi.org/10.1203/PDR.0b013e3181bf5fab DOI: https://doi.org/10.1203/PDR.0b013e3181bf5fab
  38. Blanc WA. Pathology of the placenta and cord in ascending and in haematogenous infection. Ciba Found Symp. 1979;(77):17–38. DOI: https://doi.org/10.1002/9780470720608.ch3
  39. Kraus FT. R.R., Gersell DJ, Nelson DM, Dicke JM., Placental Pathology. Washington (DC): American Registry of Pathology; 2004. DOI: https://doi.org/10.55418/1881041891
  40. Keenan WJ, Steichen JJ, Mahmood K, Altshuler G. Placental pathology compared with clinical outcome: a retrospective blind review. Am J Dis Child. 1977 Nov;131(11):1224–7. doi: https://doi.org/10.1001/archpedi.1977.02120240042009 DOI: https://doi.org/10.1001/archpedi.1977.02120240042009
  41. Rogers BB, Alexander JM, Head J, McIntire D, Leveno KJ. Umbilical vein interleukin-6 levels correlate with the severity of placental inflammation and gestational age. Hum Pathol. 2002 Mar;33(3):335–40. doi: https://doi.org/10.1053/hupa.2002.32214 DOI: https://doi.org/10.1053/hupa.2002.32214
  42. Fahmi A, Brügger M, Démoulins T, Zumkehr B, Oliveira Esteves BI, Bracher L, et al. SARS-CoV-2 can infect and propagate in human placenta explants. Cell Rep Med. 2021 Dec;2(12):100456. doi: https://doi.org/10.1016/j.xcrm.2021.100456 DOI: https://doi.org/10.1016/j.xcrm.2021.100456
  43. Stenton S, McPartland J, Shukla R, Turner K, Marton T, Hargitai B, et al. SARS-COV2 placentitis and pregnancy outcome: A multicentre experience during the Alpha and early Delta waves of coronavirus pandemic in England. EClinicalMedicine. 2022 May;47:101389. doi: https://doi.org/10.1016/j.eclinm.2022.101389 DOI: https://doi.org/10.1016/j.eclinm.2022.101389
  44. Schwartz DA, Avvad-Portari E, Babál P, Baldewijns M, Blomberg M, Bouachba A, et al. Placental Tissue Destruction and Insufficiency From COVID-19 Causes Stillbirth and Neonatal Death From Hypoxic-Ischemic Injury. Arch Pathol Lab Med. 2022 Jun;146(6):660–76. doi: https://doi.org/10.5858/arpa.2022-0029-SA DOI: https://doi.org/10.5858/arpa.2022-0029-SA
  45. Boyd TK, Redline RW. Chronic histiocytic intervillositis: a placental lesion associated with recurrent reproductive loss. Hum Pathol. 2000 Nov;31(11):1389–96. doi: https://doi.org/10.1016/S0046-8177(00)80009-X DOI: https://doi.org/10.1053/hupa.2000.19454
  46. Bos M, Harris-Mostert ET, van der Meeren LE, Baelde JJ, Williams DJ, Nikkels PG, et al. Clinical outcomes in chronic intervillositis of unknown etiology. Placenta. 2020 Feb;91:19–23. doi: https://doi.org/10.1016/j.placenta.2020.01.001 DOI: https://doi.org/10.1016/j.placenta.2020.01.001
  47. Redline RW. Villitis of unknown etiology: noninfectious chronic villitis in the placenta. Hum Pathol. 2007 Oct;38(10):1439–46. doi: https://doi.org/10.1016/j.humpath.2007.05.025 DOI: https://doi.org/10.1016/j.humpath.2007.05.025
  48. Sentilhes L, Kayem G, Ambroselli C, Provansal M, Fernandez H, Perrotin F, et al. Fertility and pregnancy outcomes following conservative treatment for placenta accreta. Hum Reprod. 2010 Nov;25(11):2803–10. doi: https://doi.org/10.1093/humrep/deq239 DOI: https://doi.org/10.1093/humrep/deq239
  49. Lausman A, McCarthy FP, Walker M, Kingdom J. Screening, diagnosis, and management of intrauterine growth restriction. J Obstet Gynaecol Can. 2012 Jan;34(1):17–28. doi: https://doi.org/10.1016/S1701-2163(16)35129-5 DOI: https://doi.org/10.1016/S1701-2163(16)35129-5
  50. Himes KP, Simhan HN. Risk of recurrent preterm birth and placental pathology. Obstet Gynecol. 2008 Jul;112(1):121–6. doi: https://doi.org/10.1097/AOG.0b013e318179f024 DOI: https://doi.org/10.1097/AOG.0b013e318179f024
  51. Gordijn SJ, Beune IM, Thilaganathan B, Papageorghiou A, Baschat AA, Baker PN, et al. Consensus definition of fetal growth restriction: a Delphi procedure. Ultrasound Obstet Gynecol. 2016 Sep;48(3):333–9. doi: https://doi.org/10.1002/uog.15884 DOI: https://doi.org/10.1002/uog.15884
  52. DGGG, O., SGGG, Intrauterine growth restriction. Guideline of the German Society of Gynecology and Obstetrics. 2016.
  53. Burton GJ, Jauniaux E. Pathophysiology of placental-derived fetal growth restriction. Am J Obstet Gynecol. 2018 Feb;218(2S 2s):S745–61. doi: https://doi.org/10.1016/j.ajog.2017.11.577 DOI: https://doi.org/10.1016/j.ajog.2017.11.577
  54. Sun C, Groom KM, Oyston C, Chamley LW, Clark AR, James JL. The placenta in fetal growth restriction: what is going wrong? Placenta. 2020 Jul;96:10–8. doi: https://doi.org/10.1016/j.placenta.2020.05.003 DOI: https://doi.org/10.1016/j.placenta.2020.05.003
  55. Vounzoulaki E, Khunti K, Abner SC, Tan BK, Davies MJ, Gillies CL. Progression to type 2 diabetes in women with a known history of gestational diabetes: systematic review and meta-analysis. BMJ. 2020 May;369:m1361. doi: https://doi.org/10.1136/bmj.m1361 DOI: https://doi.org/10.1136/bmj.m1361
  56. Correa A, Gilboa SM, Besser LM, Botto LD, Moore CA, Hobbs CA, et al. Diabetes mellitus and birth defects. Am J Obstet Gynecol. 2008 Sep;199(3):237.e1–9. doi: https://doi.org/10.1016/j.ajog.2008.06.028 DOI: https://doi.org/10.1016/j.ajog.2008.06.028
  57. Parra-Herran C, Djordjevic B. Histopathology of Placenta Creta: Chorionic Villi Intrusion into Myometrial Vascular Spaces and Extravillous Trophoblast Proliferation are Frequent and Specific Findings With Implications for Diagnosis and Pathogenesis. Int J Gynecol Pathol. 2016 Nov;35(6):497–508. doi: https://doi.org/10.1097/PGP.0000000000000250 DOI: https://doi.org/10.1097/PGP.0000000000000250
  58. Evers IM, Nikkels PG, Sikkema JM, Visser GH. Placental pathology in women with type 1 diabetes and in a control group with normal and large-for-gestational-age infants. Placenta. 2003;24(8-9):819–25. doi: https://doi.org/10.1016/S0143-4004(03)00128-0 DOI: https://doi.org/10.1016/S0143-4004(03)00128-0
  59. Asmussen I. Ultrastructure of the villi and fetal capillaries of the placentas delivered by non-smoking diabetic women (White group D). Acta Pathol Microbiol Immunol Scand [A]. 1982 Mar;90(2):95–101. doi: https://doi.org/10.1111/j.1699-0463.1982.tb00069_90A.x DOI: https://doi.org/10.1111/j.1699-0463.1982.tb00069_90A.x
  60. Björk O, Persson B. Placental changes in relation to the degree of metabolic control in diabetes mellitus. Placenta. 1982;3(4):367–78. doi: https://doi.org/10.1016/S0143-4004(82)80030-1 DOI: https://doi.org/10.1016/S0143-4004(82)80030-1
  61. Teasdale F. Histomorphometry of the human placenta in Class B diabetes mellitus. Placenta. 1983;4(1):1–12. doi: https://doi.org/10.1016/S0143-4004(83)80012-5 DOI: https://doi.org/10.1016/S0143-4004(83)80012-5
  62. Jauniaux E, Burton GJ. Villous histomorphometry and placental bed biopsy investigation in Type I diabetic pregnancies. Placenta. 2006;27(4-5):468–74. doi: https://doi.org/10.1016/j.placenta.2005.04.010 DOI: https://doi.org/10.1016/j.placenta.2005.04.010
  63. Nelson SM, Coan PM, Burton GJ, Lindsay RS. Placental structure in type 1 diabetes: relation to fetal insulin, leptin, and IGF-I. Diabetes. 2009 Nov;58(11):2634–41. doi: https://doi.org/10.2337/db09-0739 DOI: https://doi.org/10.2337/db09-0739
  64. Daskalakis G, Marinopoulos S, Krielesi V, Papapanagiotou A, Papantoniou N, Mesogitis S, et al. Placental pathology in women with gestational diabetes. Acta Obstet Gynecol Scand. 2008;87(4):403–7. doi: https://doi.org/10.1080/00016340801908783 DOI: https://doi.org/10.1080/00016340801908783
  65. Huynh J, Dawson D, Roberts D, Bentley-Lewis R. A systematic review of placental pathology in maternal diabetes mellitus. Placenta. 2015 Feb;36(2):101–14. doi: https://doi.org/10.1016/j.placenta.2014.11.021 DOI: https://doi.org/10.1016/j.placenta.2014.11.021
  66. Dubova EA, Pavlov KA, Yesayan RM, Nagovitsyna MN, Tkacheva ON, Shestakova MV, et al. Morphometric characteristics of placental villi in pregnant women with diabetes. Bull Exp Biol Med. 2011 Sep;151(5):650–4. doi: https://doi.org/10.1007/s10517-011-1406-9 DOI: https://doi.org/10.1007/s10517-011-1406-9
  67. Huynh J, Yamada J, Beauharnais C, Wenger JB, Thadhani RI, Wexler D, et al. Type 1, type 2 and gestational diabetes mellitus differentially impact placental pathologic characteristics of uteroplacental malperfusion. Placenta. 2015 Oct;36(10):1161–6. doi: https://doi.org/10.1016/j.placenta.2015.08.004 DOI: https://doi.org/10.1016/j.placenta.2015.08.004
  68. Makhseed M, Musini VM, Ahmed MA, Al-Harmi J. Placental pathology in relation to the White’s classification of diabetes mellitus. Arch Gynecol Obstet. 2002 Jul;266(3):136–40. doi: https://doi.org/10.1007/s004040100232 DOI: https://doi.org/10.1007/s004040100232
  69. Alwasel SH, Abotalib Z, Aljarallah JS, Osmond C, Al Omar SY, Harrath A, et al. The breadth of the placental surface but not the length is associated with body size at birth. Placenta. 2012 Aug;33(8):619–22. doi: https://doi.org/10.1016/j.placenta.2012.04.015 DOI: https://doi.org/10.1016/j.placenta.2012.04.015
  70. Yampolsky M, Salafia CM, Shlakhter O, Haas D, Eucker B, Thorp J. Centrality of the umbilical cord insertion in a human placenta influences the placental efficiency. Placenta. 2009 Dec;30(12):1058–64. doi: https://doi.org/10.1016/j.placenta.2009.10.001 DOI: https://doi.org/10.1016/j.placenta.2009.10.001
  71. Schwartz N, Mandel D, Shlakhter O, Coletta J, Pessel C, Timor-Tritsch IE, et al. Placental morphologic features and chorionic surface vasculature at term are highly correlated with 3-dimensional sonographic measurements at 11 to 14 weeks. J Ultrasound Med. 2011 Sep;30(9):1171–8. doi: https://doi.org/10.7863/jum.2011.30.9.1171 DOI: https://doi.org/10.7863/jum.2011.30.9.1171
  72. Hecht JL, Baergen R, Ernst LM, Katzman PJ, Jacques SM, Jauniaux E, et al. Classification and reporting guidelines for the pathology diagnosis of placenta accreta spectrum (PAS) disorders: recommendations from an expert panel. Mod Pathol. 2020 Dec;33(12):2382–96. doi: https://doi.org/10.1038/s41379-020-0569-1 DOI: https://doi.org/10.1038/s41379-020-0569-1
  73. Benirschke K. B.G., Baergen RN., Pathology of the human placenta. 6th edition. 2012. DOI: https://doi.org/10.1007/978-3-642-23941-0
  74. Linn RL, Miller ES, Lim G, Ernst LM. Adherent basal plate myometrial fibers in the delivered placenta as a risk factor for development of subsequent placenta accreta. Placenta. 2015 Dec;36(12):1419–24. doi: https://doi.org/10.1016/j.placenta.2015.10.004 DOI: https://doi.org/10.1016/j.placenta.2015.10.004
  75. Miller ES, Linn RL, Ernst LM. Does the presence of placental basal plate myometrial fibres increase the risk of subsequent morbidly adherent placenta: a case-control study. BJOG. 2016 Dec;123(13):2140–5. doi: https://doi.org/10.1111/1471-0528.13579 DOI: https://doi.org/10.1111/1471-0528.13579
  76. Jauniaux E, Jurkovic D. Placenta accreta: pathogenesis of a 20th century iatrogenic uterine disease. Placenta. 2012 Apr;33(4):244–51. doi: https://doi.org/10.1016/j.placenta.2011.11.010 DOI: https://doi.org/10.1016/j.placenta.2011.11.010
  77. Vinograd A, Wainstock T, Mazor M, Mastrolia SA, Beer-Weisel R, Klaitman V, et al. A prior placenta accreta is an independent risk factor for post-partum hemorrhage in subsequent gestations. Eur J Obstet Gynecol Reprod Biol. 2015 Apr;187:20–4. doi: https://doi.org/10.1016/j.ejogrb.2015.01.014 DOI: https://doi.org/10.1016/j.ejogrb.2015.01.014
  78. Roeca C, Little SE, Carusi DA. Pathologically Diagnosed Placenta Accreta and Hemorrhagic Morbidity in a Subsequent Pregnancy. Obstet Gynecol. 2017 Feb;129(2):321–6. doi: https://doi.org/10.1097/AOG.0000000000001843 DOI: https://doi.org/10.1097/AOG.0000000000001843
  79. Kingdom JC, Audette MC, Hobson SR, Windrim RC, Morgen E. A placenta clinic approach to the diagnosis and management of fetal growth restriction. Am J Obstet Gynecol. 2018 Feb;218(2S 2s):S803–17. doi: https://doi.org/10.1016/j.ajog.2017.11.575 DOI: https://doi.org/10.1016/j.ajog.2017.11.575
  80. Thompson JM, Irgens LM, Skjaerven R, Rasmussen S. Placenta weight percentile curves for singleton deliveries. BJOG. 2007 Jun;114(6):715–20. 10.1111/j.1471-0528.2007.01327.x DOI: https://doi.org/10.1111/j.1471-0528.2007.01327.x
  81. Vogel M, Turowski G, eds. Clinical Pathology of the Placenta. Berlin: De Gruyter; 2019. 10.1515/9783110452600 DOI: https://doi.org/10.1515/9783110452600

Most read articles by the same author(s)