Аllergic Basal Deciduitis as a Reason of Recurrent Antenatal Fetal Death

Authors

  • Yevgeniy Kamyshanskiy Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan https://orcid.org/0000-0001-8975-3612
  • Olga Kostyleva Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan https://orcid.org/0000-0003-2250-6670
  • Maida Tussupbekova Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan https://orcid.org/0000-0003-3105-4450
  • Leila Stabayeva Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan https://orcid.org/0000-0001-8598-1829
  • Gulnazira Imanbayeva Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan https://orcid.org/0000-0002-9091-4601
  • Raihan Nygyzbayeva Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan https://orcid.org/0000-0001-6264-1872
  • Evgeniy Kotov Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan
  • Denis Kossitsyn Department of Pathology, Karaganda Medical University, Karaganda, Kazakhstan

DOI:

https://doi.org/10.3889/oamjms.2021.6129

Keywords:

Pregnant, Chronic placental insufficiency, Allergic status, Placental-fetal compartment

Abstract

BACKGROUND: Allergic diseases of pregnant women are associated with chronic placental insufficiency and the development of immunopathological conditions of unknown etiology in a child in postnatal life. Pregnancy with bronchial asthma is often complicated by intrauterine growth retardation, preeclampsia, and antenatal fetal death.

AIM: The objective was to present a clinical case of recurrent antenatal fetal death in the third trimester in women with bronchial asthma under controlled course.

CASE REPORT: Pregnancy proceeded without clinical signs of exacerbation of bronchial asthma and allergic status. However, chronic inflammation with eosinophilia in the intervillous space and the basal lamina was revealed in the placenta tissue. Eosinophilia of the intervillous area was accompanied by obliteration of the intervillous area by fibrin deposits.

CONCLUSION: We suppose that immunological inflammation at the fetoplacental unit level can occur regardless of the mother’s allergic status. Moreover, it is likely that the objective state of the mother in the presence of an allergic disease does not reflect the presence/absence of an immunological process in the placenta, as the immunological inflammatory process can develop in different compartments (at the level of the mother’s body and the placental-fetal compartment) with varying degrees of severity.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Plum Analytics Artifact Widget Block

References

Gould HJ, Sutton BJ, Beavil AJ, Beavil RL, McCloskey N, Coker HA, et al. The biology of IGE and the basis of allergic disease. Annu Rev Immunol. 2003;21:579-28. https://doi.org/10.1146/annurev.immunol.21.120601.141103 PMid:12500981 DOI: https://doi.org/10.1146/annurev.immunol.21.120601.141103

Punnonen J, Aversa GG, Vandekerckhove B, Roncarolo MG, de Vries JE. Induction of isotype switching and Ig production by CD5+ and CD10+ human fetal B cells. J Immunol. 1992;148(11):3398-404. PMid:1375243

Bain E, Pierides KL, Clifton VL, Hodyl NA, Stark MJ. Interventions for managing asthma in pregnancy. Cochrane Database Syst Rev. 2014;2014(10):CD010660. https://doi.org/10.1002/14651858.cd010660.pub2 PMid:25331331 DOI: https://doi.org/10.1002/14651858.CD010660.pub2

Sheiner E, Mazor M, Levy A, Wiznitzer A, Bashiri A. Pregnancy outcome of asthmatic patients: A population-based study. J Matern Fetal Neonatal Med. 2005;18(4):237-40. https://doi.org/10.1080/14767050500260616 PMid:16318973 DOI: https://doi.org/10.1080/14767050500260616

Alcazar MA, Nusken Е, Nuesken К. Programming intrauterine deficiency. In: Monatsschrift Kinderheilkunde. Vol. 164. Berlin, Germany: Springer; 2016. p. 106. https://doi.org/10.1007/s00112-015-3420-x DOI: https://doi.org/10.1007/s00112-015-3420-x

Murphy VE, Gibson PG, Smith R, Clifton VL. Asthma during pregnancy: Mechanisms and treatment implications. Eur Resp J. 2005;25(4):731-50. PMid:15802351 DOI: https://doi.org/10.1183/09031936.05.00085704

Prada JA, Tsang RC. Biological mechanisms of environmentally induced causes of IUGR. Eur J Clin Nutr. 1998;52(1):21-8. PMid:9511016

Liu S, Wen SW, Demissie K, Marcoux S, Kramer MS. Maternal asthma and pregnancy outcomes: A retrospective cohort study. Am J Obstet Gynecol. 2001;184(2):90-6. https://doi.org/10.1067/mob.2001.108073 PMid:11174486 DOI: https://doi.org/10.1067/mob.2001.108073

Dudenhausen JW, Maier RF. Perinatal problems in multiple births. Dtsch Ärztebl Int. 2010;107(38):663-8. PMid:20953254 DOI: https://doi.org/10.3238/arztebl.2010.0663

Vogel M. Atlas der Morphologischen Plazentadiagnostik. 2nd ed. Heidelberg: Springer-Verlag; 1996. DOI: https://doi.org/10.1007/978-3-642-80083-2

Vogel M, Kloppel G, Kreipe H, Remmele W. Pathologie der Plazenta: Spatschwangerschaft und fetoplazentare Einheit, Pathologie. Heidelberg: Springer-Verlag; 2013. p. 519. https://doi.org/10.1007/978-3-642-04564-6_25 DOI: https://doi.org/10.1007/978-3-642-04564-6_25

Benirschke K, Kaufmann P, Baergen R. Pathology of the Human Placenta. 5th ed. New York: Springer; 2006.

Kapur P, Rakheja D, Gomez AM, Sheffield J, Sanchez P, Rogers BB. Characterization of inflammation in syphilitic villitis and in villitis of unknown etiology. Pediatr Dev Pathol. 2004;7(5):453-8. https://doi.org/10.1007/s10024-004-2124-3 PMid:15547769 DOI: https://doi.org/10.1007/s10024-004-2124-3

Myerson D, Parkin RK, Benirschke K, Tschetter CN, Hyde SR. The pathogenesis of villitis of unknown etiology: Analysis with a new conjoint immunohistochemistry-in situ hybridization procedure to identify maternal and fetal cells. Pediatr Dev Pathol. 2006;9(4):257-65. https://doi.org/10.2350/08-05-0103.1 PMid:16944988 DOI: https://doi.org/10.2350/08-05-0103.1

Redline RW, Patterson P. Patterns of placental injury: Correlations with gestational age, placental weight, and clinical diagnoses. Arch Pathol Lab Med. 1994;118(7):698-701. PMid:8024402

Redline RW, Abramowsky CR. Clinical and pathologic aspects of recurrent placental villitis. Hum Pathol. 1985;16(7):727-31. https://doi.org/10.1016/s0046-8177(85)80159-3 PMid:4007849 DOI: https://doi.org/10.1016/S0046-8177(85)80159-3

Russell P, Atkinson K, Krishnan L. Recurrent reproductive failure due to severe placental villitis of unknown etiology. J Reprod Med. 1980;24(2):93-98. PMid:7359507

Katzman PJ, Oble DA. Eosinophilic/T-cell chorionic vasculitis and chronic villitis involve regulatory T cells and often occur together. Pediatr Dev Pathol. 2013;16(4):278-91. https://doi.org/10.2350/12-10-1258-oa.1 PMid:23600955 DOI: https://doi.org/10.2350/12-10-1258-OA.1

Katzman PJ, Li L, Wang N. Identification of fetal inflammatory cells in eosinophilic/T-cell chorionic vasculitis using fluorescent in situ hybridization. Pediatr Dev Pathol. 2015;18(4):305-9. PMid:25756311 DOI: https://doi.org/10.2350/14-12-1585-OA.1

Jacques SM, Qureshi F, Kim CJ, Lee JH, Giorgadze T, Mittal P, et al. Eosinophilic/T-cell chorionic vasculitis: A clinicopathologic and immuno-histochemical study of 51 cases. Pediatr Dev Pathol. 2011;14(3):198-205. https://doi.org/10.2350/10-07-0867-oa.1 PMid:21050080 DOI: https://doi.org/10.2350/10-07-0867-OA.1

Chung EK, Miller RL, Wilson MT, McGeady SJ, Culhane JF. Antenatal risk factors, cytokines and the development of atopic disease in early childhood. Arch Dis Child Fetal Neonatal Ed. 2007;92(1):F68-73. https://doi.org/10.1136/adc.2006.106492 PMid:17185433 DOI: https://doi.org/10.1136/adc.2006.106492

Prescott SL, Clifton V. Asthma and pregnancy: Emerging evidence of epigenetic interactions in utero. Curr Opin Allergy Clin Immunol. 2009;9(5):417-26. https://doi.org/10.1097/aci.0b013e328330634f PMid:19652594 DOI: https://doi.org/10.1097/ACI.0b013e328330634f

Kumar R. Prenatal factors and the development of asthma. Curr Opin Pediatr. 2008;20(6):682-7. PMid:19005336 DOI: https://doi.org/10.1097/MOP.0b013e3283154f26

Joerink M, Rindsjö E, Stenius F, Alm J, Lilja G, Grönlund H, et al. Evidence for allergen-specific IgE of maternal origin in human placenta. Allergy. 2009;64(6):905-12. https://doi.org/10.1111/j.1398-9995.2009.01941.x PMid:19220215 DOI: https://doi.org/10.1111/j.1398-9995.2009.01941.x

Rindsjo E, Varli IH, Ofori MF, Lundquist M, Holmlund U, Papadogiannakis N, et al. Presence of IgE cells in human placenta is independent of malaria infection or chorioamnionitis. Clin Exp Immunol. 2006;144(2):204-11. https://doi.org/10.1111/j.1365-2249.2006.03055.x PMid:16634792 DOI: https://doi.org/10.1111/j.1365-2249.2006.03055.x

Hanzlikova J, Ulcova-Gallova Z, Malkusova I, Sefrna F, Panzner P. TH1-TH2 response and the atopy risk in patients with reproduction failure. Am J Eprod Immunol. 2009;61(3):213-20. https://doi.org/10.1111/j.1600-0897.2009.00683.x PMid:19239423 DOI: https://doi.org/10.1111/j.1600-0897.2009.00683.x

Jones CA, Warner JA, Warner JO. Fetal swallowing of IgE. Lancet. 1998;351(9119):1859. https://doi.org/10.1016/s0140-6736(05)78805-x PMid:9652674 DOI: https://doi.org/10.1016/S0140-6736(05)78805-X

Maurer D, Ebner C, Reininger B, Fiebiger E, Kraft D, Kinet JP, et al. The high affinity IgE receptor (Fc epsilon RI) mediates IgE-dependent allergen presentation. J Immunol. 1995;154(12):6285-90. PMid:7759866

Downloads

Published

2021-06-26

How to Cite

1.
Kamyshanskiy Y, Kostyleva O, Tussupbekova M, Stabayeva L, Imanbayeva G, Nygyzbayeva R, Kotov E, Kossitsyn D. Аllergic Basal Deciduitis as a Reason of Recurrent Antenatal Fetal Death. Open Access Maced J Med Sci [Internet]. 2021 Jun. 26 [cited 2024 Nov. 21];9(C):80-3. Available from: https://oamjms.eu/index.php/mjms/article/view/6129

Issue

Section

Case Reports in Gynecology and Obstetrics

Categories