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Umbilical cord constriction as a cause of intrauterine fetal death

ABSTRACT

The umbilical cord constriction (UCC) is an uncommon condition and an important etiology for stillborn fetuses. The main goal of this study was to verify the UCC occurrence as the cause of intrauterine fetal death, the associated etiology and its pathological characteristics. Therefore, a descriptive retrospective cross-sectional study was developed using the database from a Pathology Institute, in Brazil, from 1995 to 2017. The results presented a total of 1,359 embryo/fetus deaths – 69 (5.07%) due to UCC, 60.9% males and 39.1% females. The average age of pregnant women was 27.5 years ± 7.2 years of standard deviation (SD). The majority of deaths occurred during the second trimester (76.5%), followed by the first (14.7%) and third (8.8%) trimesters, respectively. One constriction alone was found in 87% of cases, 11% had two constrictions and only 1% had three or more. The presence of congenital malformations was detected in 20.2% of necropsies, the identification of chronic fetal distress was described in 71% of the technical reports and 17% of the cases had obstructive vasculopathy characteristics in microscopy analysis. Regarding the anatomopathological characteristics between the male and female sexes, no significant difference was found (p > 0.05) correlating gestational age, weight or congenital malformations. UCC was a cause of fetal death found in 5% of the cases, and it was linked to congenital malformations, fetal distress and obliterative vasculopathy.

Key words:
fetal death; fetal distress; umbilical cord

RESUMEN

La constricción del cordón umbilical (CCU) es una condición infrecuente que no está bien descrita en la literatura, a pesar de ser una importante etiología observada en mortinatos. El objetivo de este estudio fue verificar la ocurrencia de CCU como causa de muerte fetal y las características patológicas asociadas. Para ello, se llevó a cabo un estudio retrospectivo transversal con informaciones de la base de datos de un Instituto de Patología, en Brasil, de 1995 hasta 2017. Los resultados fueron: 1.359 muertes de embriones/fetos, de las cuales 69 (5,07%) se debieron a CCU; 60,9% eran del sexo masculino y 39,1%, del femenino. El promedio de edad de las mujeres embarazadas fue de 27,5 anos; desviación estándar de ± 7,2 anos. La mayoría de las muertes ocurrió en el segundo trimestre (76,5%), seguido del primero (14,7%) y del tercero (8,8%). Entre el total de casos de CCU observados, 87% tuvieron sólo una constricción; 11%, dos; y 1%, tres o más. La presencia de malformaciones congénitas fue encontrada en 20,2% de las necropsias; la identificación de sufrimiento fetal crónico fue reportada en 71% de los informes; y características de vasculopatía obstructiva en el análisis de microscopía, en 17% de los casos. Con respecto a las características anatomopatológicas entre los sexos masculino y femenino, no se encontró ninguna diferencia significativa (p > 0,05) correlacionando edad gestacional de los fetos/embriones, peso o malformaciones congénitas. La CCU es una condición rara de muerte fetal asociada a bajo peso fetal y restricción de crecimiento. Nuestra investigación sugiere una posible relación entre la CCU y la vasculopatía obliterativa.

Palabras clave:
muerte fetal; sufrimiento fetal; cordón umbilical

RESUMO

A constrição de cordão umbilical (CCU) é uma condição infrequente, não bem descrita na literatura, apesar de ser uma importante etiologia observada em fetos natimortos. O objetivo deste estudo foi verificar a ocorrência de CCU como causa de morte fetal e as características etiopatológicas associadas. Para tanto, um estudo retrospectivo transversal foi realizado a partir das informações do banco de dados do Instituto de Patologia de Passo Fundo, durante os anos de 1995 a 2017. Os resultados foram: 1.359 mortes de embriões/fetos, das quais 69 (5,07%) foram devidas a CCU; 60,9% eram do sexo masculino e 39,1%, do feminino. A média de idade das gestantes foi de 27,5 anos; desvio padrão (DP) de ± 7,2 anos. A maioria das mortes ocorreu no segundo trimestre (76,5%), seguido pelo primeiro (14,7%) e terceiro (8,8%). Entre o total de CCU observadas, 87% tiveram ocorrência de apenas uma constrição; 11%, de duas; e 1%, de três ou mais. A presença de malformações congênitas foi encontrada em 20,2% das necropsias; a identificação de sofrimento fetal crônico foi relatada em 71% dos laudos; e características de vasculopatia obstrutiva na análise da microscopia, em 17% dos casos. Em relação às características anatomopatológicas entre os sexos masculino e feminino, nenhuma diferença significativa (p > 0,05) foi encontrada correlacionando idade gestacional dos fetos/embriões, peso ou malformações congênitas. A CCU é uma condição incomum de morte fetal associada a baixo peso fetal e restrição de crescimento. Nossa pesquisa sugere uma possível relação entre a CCU e a vasculopatia obliterativa.

Unitermos:
morte fetal; sofrimento fetal; cordão umbilical

INTRODUCTION

The gestational process is associated with significant uterine and systemic hemodynamic changes, to cope with the metabolic demands of both mother and developing fetus. Although the female body keeps a dynamic balance by compensatory mechanisms, the boundaries between normality and disease are ill-defined, and their unbalance represents high risks of maternal-fetal morbidity and mortality(11 Salge AKM, Silva RCR, Guimarães JV, Ramalho WS, Abdalla DR, Abdalla GK. Relação entre os aspectos clínicos, placentários, obstétricos e neonatais e o crescimento intrauterino na gestação de alto risco. Texto e Context Enferm. 2017; 26(2): 1-9.

2 Artico LG, Madi JM, Godoy AEG, Coelho CP, Rombaldi RL, Artico GR. Alterações histopatológicas em placentas humanas relacionadas às síndromes hipertensivas. Rev Bras Ginecol Obs. 2009; 31(1): 10-6.
-33 Silva TG, Lima TABCL, Mota AVP, Gueder V. A importância do exame anatomopatológico da placenta em obstetrícia e neonatologia. HU Rev. 2016; 42(3): 171-5.).

The umbilical cord allows the placenta-fetus communication, playing an important role in immunological surveillance and maternal tolerance to the fetus. In obstetrics, the umbilical cord provides valuable information about pregnancy evolution. Thus, any alteration could cause damage in fetal development, anomalies, perinatal complications or even intrauterine fetal death. For example, when umbilical cord constriction (UCC) occurs near the fetus abdominal wall it causes fetal death(44 Collins JH. Umbilical cord accidents: human studies. Semin Perinatol. 2002; 26(1): 79-82.

5 Peng HQ, Levitin-Smith M, Rochelson B, Kahn E. Umbilical cord stricture and overcoiling are common causes of fetal demise. Pediatr Dev Pathol. 2006;9(1): 14-19.

6 Hershkovitz R, Silberstein T, Sheiner E, et al. Risk factors associated with true knots of the umbilical cord. Eur J Obstet Gynecol Reprod Biol. 2001; 98(1): 36-9.
-77 Heifetz SA. Strangulation of the umbilical cord by amniotic bands: report of six cases and literature review. Pediatr Pathol. 1984; 2: 285-304.).

The UCC is an infrequent and not well described condition and still has no formally accepted etiology in the literature. Nevertheless, its recognition is easy and based on macroscopic identification(11 Salge AKM, Silva RCR, Guimarães JV, Ramalho WS, Abdalla DR, Abdalla GK. Relação entre os aspectos clínicos, placentários, obstétricos e neonatais e o crescimento intrauterino na gestação de alto risco. Texto e Context Enferm. 2017; 26(2): 1-9.,88 Sheppard SJ, Khalil RA. Risk factors and mediators of the vascular dysfunction associated with hypertension in pregnancy. Cardiovasc Hematol Disord Drug Targets. 2011; 10(1): 33-52.

9 Rodríguez JI, Mariño-Enríquez A, Suárez-Aguado J, Lapunzina P. Umbilical cord stricture is not a genetic anomaly: a study in twins. Pediatr Dev Pathol. 2008; 11(5): 363-9.
-1010 Neves C, Medina JL, Delgado JL. Alterações endócrinas e imunomodulação na gravidez. Arq Med. 2007; 21(5-6): 175-82.). Some studies have reported a prevalence of 10%-20% of fetal deaths related to UCC. Umbilical cord stenosis may also be present, but is generally associated with other anomalies such as torsion or excessive length of the cord(22 Artico LG, Madi JM, Godoy AEG, Coelho CP, Rombaldi RL, Artico GR. Alterações histopatológicas em placentas humanas relacionadas às síndromes hipertensivas. Rev Bras Ginecol Obs. 2009; 31(1): 10-6.,88 Sheppard SJ, Khalil RA. Risk factors and mediators of the vascular dysfunction associated with hypertension in pregnancy. Cardiovasc Hematol Disord Drug Targets. 2011; 10(1): 33-52.,1111 Queiroz APS, Costa CFF. Amadurecimento precoce da placenta avaliada pela ultrassonografia e prognóstico perinatal. Rev Bras Ginecol Obs. 2008; 28(3): 165-70.).

The UCC has as a pathological feature that decreases Wharton’s jelly (a connective tissue matrix responsible for protecting the umbilical vessels), what predisposes to torsions, edema, fibrosis and thrombosis. Therefore, there is a decrease in fetal blood flow leading to fetal distress and death(1212 Kim EN, Shim J, Kim CJ. Wharton jelly hair in a case of umbilical cord stricture and fetal death. J Pathol Transl Med. 2019; 53: 145-7.,1313 Masliah E, Wahl C. Umbilical cord stricture in a 21-week fetus. J Perinatol. 2004; 24: 48-49.).

This anomaly has traditionally been considered sporadic, which implied a very low risk of recurrence in subsequent pregnancies. However, some studies showed consecutive abortions due to umbilical stenosis, raising the question of the presence of a genetic component(1414 Ling S, Hwang J, Huang L. Umbilical cord stricture causing intrauterine fetal death in a 22-week fetus. Taiwan J Obstet Gynecol. 2006; 45(1): 73-5.,1515 Tan SJ, Chen CH, Wu GJ, Chen WHC, Chang CC. Fetal demise by umbilical cord around abdomen and stricture. Arch Gynecol Obs. 2010; 281: 137-9.

16 Reis MR. Alterações macroscópicas do cordão umbilical em gestações de alto risco e suas repercussões [dissertation]. Goiás: Universidade Federal de Goiás; 2014.
-1717 Hasegawa J, Mimura T, Morimoto T, et al. Detection of umbilical venous constriction by Doppler flow measurement at midgestation. Ultrasound Obstet Gynecol. 2010; 36(2): 196-201.).

The present study aimed to verify the occurrence of UCC as a cause of fetal death and its etiopathological characteristics.

METHODS

A retrospective cross-sectional study using the database of the Pathology Institute of Passo Fundo (IPPF). The IPPF is located in the north of the state of Rio Grande do Sul, Brazil. The database involved all the fetal death occurrences (1,359) from 1995 to 2017, from which only cases of umbilical cord constriction were elected, amounting to 69 cases (5.07%).

The variables analyzed in the study were maternal age, gestational age, placental and fetal/embryo weight, presence of a single umbilical artery, umbilical cord measurements, total fetal/embryo length, sex, presence or absence of chronic fetal distress, congenital malformations, circular cord and obstructive vasculopathy of villi vessels.

Statistical analysis was performed using GraphPad Prism 6 statistical software and Microsoft Excel 2010. Statistical comparisons between the years were made with the Student’s t test for parametric variables and Mann-Whitney test for non-parametric variables. Values of p < 0.05 were considered significant.

The study was approved by the Research Ethics Committee of Universidade de Passo Fundo, under number 04477218.1.0000.5342.

RESULTS

Among the total of 1,359 fetal deaths, only 69 cases were caused by UCC. The average maternal age was 27.5 years ± 7.2 years of standard deviation (SD). No multiple cases happened to the same woman. As regards the pregnancy period, most cases happened in the second trimester (76.5%), followed by first (14.7%) and third (8,8%) trimesters (Figure).

FIGURE
Visual demonstration of the percentages of confirmed cases of umbilical cord constrictions during the trimesters of pregnancy

The placenta characteristics were: average weight of 116 g (SD ± 76), umbilical cord length of 20.9 cm (SD ± 10.9) and thickness of 0.87 cm (SD ± 0.37). The difference between normal cord thickness and the caliber in the stenosis area was 77%, decreased at the constriction surrounding. Only 7% of the cases presented a single umbilical artery. One constriction was found in 87%, two in 11%, and three or more constrictions in just 1% of all cases (Table 1).

TABLE 1
Description of the anatomopathological characteristics of the placenta and umbilical cord

The average embryo/fetus weight was 235 g [confidence interval (CI) 95%, 178-285], with total length of 19.65 cm (SD ± 6.5); 60.9% were males and 39.1% females. Presence of congenital malformations was described in 20.2% of necropsies; many of those were synchronous in the same individual. The most prevalent malformation occurred in the lower limbs (8.6%): half of them affected the embryos feet. Other malformations included: single umbilical artery (7%), colonic rotation (4.3%), and renal agenesis (4.3%). Identification of chronic fetus distress was reported in 71% of cases, nuchal cord in 10%, and characteristics of obstructive vasculopathy in microscopy analysis in 17% (Table 2).

TABLE 2
Description of the anatomopathological characteristics of embryos/fetuses

Concerning the anatomopathological characteristics between male and female fetuses, no significance was found correlating gestational age, birth weight or congenital malformations.

DISCUSSION

Maternal age is usually associated with several outcomes throughout pregnancy. However, as shown in the present study, there was no correlation between maternal age and UCC(99 Rodríguez JI, Mariño-Enríquez A, Suárez-Aguado J, Lapunzina P. Umbilical cord stricture is not a genetic anomaly: a study in twins. Pediatr Dev Pathol. 2008; 11(5): 363-9.,1818 Radulescu L, Ferechide D, Popa F. The importance of fetal gender in intrauterine growth restriction. J Med Life. 2013; 6: 320-4.,1919 Ragonesi S, Bertini A, Camano L. Crescimento intrauterino retardado: aspectos atuais. Rev Assoc Med Bras. 1997; 43: 173-8.).

Corroborating the literature, the study showed an increase in the probability of new stenosis in a subsequent gestation in cases of pregnancies previously diagnosed with UCC. Nevertheless, the absence of this recurrence is still questioned, bringing up doubts about the involvement of a genetic component that may allow recidivism(99 Rodríguez JI, Mariño-Enríquez A, Suárez-Aguado J, Lapunzina P. Umbilical cord stricture is not a genetic anomaly: a study in twins. Pediatr Dev Pathol. 2008; 11(5): 363-9.,1212 Kim EN, Shim J, Kim CJ. Wharton jelly hair in a case of umbilical cord stricture and fetal death. J Pathol Transl Med. 2019; 53: 145-7.,1313 Masliah E, Wahl C. Umbilical cord stricture in a 21-week fetus. J Perinatol. 2004; 24: 48-49.,1515 Tan SJ, Chen CH, Wu GJ, Chen WHC, Chang CC. Fetal demise by umbilical cord around abdomen and stricture. Arch Gynecol Obs. 2010; 281: 137-9.). Many cases of UCC have been reported, but only few studies aimed to investigate the possibility of an associated genetic component increasing the risk of recurrence in further pregnancies. Amongst them, the largest accomplished study concluded that there is a minimal or null genetic component in UCC (1.5%) in pregnancies following previous malformation(99 Rodríguez JI, Mariño-Enríquez A, Suárez-Aguado J, Lapunzina P. Umbilical cord stricture is not a genetic anomaly: a study in twins. Pediatr Dev Pathol. 2008; 11(5): 363-9.).

Regarding the period of involvement in pregnancy, the highest rate of cord stenosis diagnosis occurs in the second trimester, followed by the first and third trimesters(2020 Marsál K. Intrauterine growth restriction. Curr Opin Obs Gynecol. 2002; 14(2): 127-35.,2121 Kupferminc MJ. Mid-trimester severe intrauterine growth restriction is associated with a high prevalence of thrombophilia. BJOG. 2002; 109: 1373-6.), matching the data of the present study.

According to the literature, the presence of a single umbilical artery is not related to an increase in fetal mortality(2222 Luo X, Zhai S, Shi N, Li M, Cui S, Xu Y. The risk factors and neonatal outcomes of isolated single umbilical artery in singleton pregnancy: a meta-analysis. Sci Reports. 2017; 7: 7396.), confirming the findings of our study, since only 7% of the 69 cases presented such abnormality. Concerning placenta weight, umbilical cord length and number of constrictions, the shortage of data in the literature prevents comparison to the findings of this study. Nevertheless, this paper is the first to show significant data about placenta weight, umbilical cord length and number of constrictions, and allows further correlations to be investigated.

Low fetal weight and low total length observed in the anatomopathological reports of the present study may indicate UCC as one of the etiologies of intrauterine growth restriction (IUGR)(1919 Ragonesi S, Bertini A, Camano L. Crescimento intrauterino retardado: aspectos atuais. Rev Assoc Med Bras. 1997; 43: 173-8.,2020 Marsál K. Intrauterine growth restriction. Curr Opin Obs Gynecol. 2002; 14(2): 127-35.,2323 Khoury M, Erickson J, Cordero J. Congenital malformations and intrauterine growth retardation: a population study. Pediatrics. 1988; 82: 830-90.).

IUGR is identified when fetal weight is ranked below the 10th percentile for gestational age, being a common clinical problem associated with increased perinatal morbidity and mortality. Another finding that corroborates this hypothesis is the chronic fetal distress, identified in 71% of sampled fetuses, a finding often associated with fetal-placental alterations in IUGR patients. Besides that, the presence of congenital malformations in 20.2% of samples validates IUGR as a possible etiology, since there is an association between fetal malformations and IUGR(2323 Khoury M, Erickson J, Cordero J. Congenital malformations and intrauterine growth retardation: a population study. Pediatrics. 1988; 82: 830-90.).

Our study suggested a prevalence of cord constriction in males. This finding contradicts previous IUGR studies that indicated a higher prevalence in females(1818 Radulescu L, Ferechide D, Popa F. The importance of fetal gender in intrauterine growth restriction. J Med Life. 2013; 6: 320-4.). However, it is important to highlight that there is no distinction concerning gender among the possible etiologies of growth restriction in the literature. This may have been the reason why cord stenosis prevalence had such discrepancies with previously existing data.

Another fact that may corroborate a possible association between the conditions is that fetuses with IUGR, specifically after the second trimester, could have their growth restricted by thrombophilia, although studies are still controversial(2121 Kupferminc MJ. Mid-trimester severe intrauterine growth restriction is associated with a high prevalence of thrombophilia. BJOG. 2002; 109: 1373-6.,2424 Rodger M, Paidas M, Claire M. Inherited thrombophilia and pregnancy complications revisited. Obs Gynecol. 2008; 112: 320-4.). Furthermore, the presence of obliterative vasculopathy in 17% of the samples may indicate a possible association between pathologies as thrombophilia and UCC, since obstructive vasculopathy is a common finding in histopathological reports of patients with thrombophilia(2424 Rodger M, Paidas M, Claire M. Inherited thrombophilia and pregnancy complications revisited. Obs Gynecol. 2008; 112: 320-4.). However, further studies are needed to elucidate the possible association between these factors.

CONCLUSION

UCC was a cause of fetal death in 5% of cases of the present study. A link with congenital malformations was established in 20% of the sample, fetal distress in 71%, and obliterative vasculopathy in 17%. The obliterative vasculopathy finding, reported in thrombophilia, suggests a possible correlation between these two conditions.

REFERENCES

  • 1
    Salge AKM, Silva RCR, Guimarães JV, Ramalho WS, Abdalla DR, Abdalla GK. Relação entre os aspectos clínicos, placentários, obstétricos e neonatais e o crescimento intrauterino na gestação de alto risco. Texto e Context Enferm. 2017; 26(2): 1-9.
  • 2
    Artico LG, Madi JM, Godoy AEG, Coelho CP, Rombaldi RL, Artico GR. Alterações histopatológicas em placentas humanas relacionadas às síndromes hipertensivas. Rev Bras Ginecol Obs. 2009; 31(1): 10-6.
  • 3
    Silva TG, Lima TABCL, Mota AVP, Gueder V. A importância do exame anatomopatológico da placenta em obstetrícia e neonatologia. HU Rev. 2016; 42(3): 171-5.
  • 4
    Collins JH. Umbilical cord accidents: human studies. Semin Perinatol. 2002; 26(1): 79-82.
  • 5
    Peng HQ, Levitin-Smith M, Rochelson B, Kahn E. Umbilical cord stricture and overcoiling are common causes of fetal demise. Pediatr Dev Pathol. 2006;9(1): 14-19.
  • 6
    Hershkovitz R, Silberstein T, Sheiner E, et al. Risk factors associated with true knots of the umbilical cord. Eur J Obstet Gynecol Reprod Biol. 2001; 98(1): 36-9.
  • 7
    Heifetz SA. Strangulation of the umbilical cord by amniotic bands: report of six cases and literature review. Pediatr Pathol. 1984; 2: 285-304.
  • 8
    Sheppard SJ, Khalil RA. Risk factors and mediators of the vascular dysfunction associated with hypertension in pregnancy. Cardiovasc Hematol Disord Drug Targets. 2011; 10(1): 33-52.
  • 9
    Rodríguez JI, Mariño-Enríquez A, Suárez-Aguado J, Lapunzina P. Umbilical cord stricture is not a genetic anomaly: a study in twins. Pediatr Dev Pathol. 2008; 11(5): 363-9.
  • 10
    Neves C, Medina JL, Delgado JL. Alterações endócrinas e imunomodulação na gravidez. Arq Med. 2007; 21(5-6): 175-82.
  • 11
    Queiroz APS, Costa CFF. Amadurecimento precoce da placenta avaliada pela ultrassonografia e prognóstico perinatal. Rev Bras Ginecol Obs. 2008; 28(3): 165-70.
  • 12
    Kim EN, Shim J, Kim CJ. Wharton jelly hair in a case of umbilical cord stricture and fetal death. J Pathol Transl Med. 2019; 53: 145-7.
  • 13
    Masliah E, Wahl C. Umbilical cord stricture in a 21-week fetus. J Perinatol. 2004; 24: 48-49.
  • 14
    Ling S, Hwang J, Huang L. Umbilical cord stricture causing intrauterine fetal death in a 22-week fetus. Taiwan J Obstet Gynecol. 2006; 45(1): 73-5.
  • 15
    Tan SJ, Chen CH, Wu GJ, Chen WHC, Chang CC. Fetal demise by umbilical cord around abdomen and stricture. Arch Gynecol Obs. 2010; 281: 137-9.
  • 16
    Reis MR. Alterações macroscópicas do cordão umbilical em gestações de alto risco e suas repercussões [dissertation]. Goiás: Universidade Federal de Goiás; 2014.
  • 17
    Hasegawa J, Mimura T, Morimoto T, et al. Detection of umbilical venous constriction by Doppler flow measurement at midgestation. Ultrasound Obstet Gynecol. 2010; 36(2): 196-201.
  • 18
    Radulescu L, Ferechide D, Popa F. The importance of fetal gender in intrauterine growth restriction. J Med Life. 2013; 6: 320-4.
  • 19
    Ragonesi S, Bertini A, Camano L. Crescimento intrauterino retardado: aspectos atuais. Rev Assoc Med Bras. 1997; 43: 173-8.
  • 20
    Marsál K. Intrauterine growth restriction. Curr Opin Obs Gynecol. 2002; 14(2): 127-35.
  • 21
    Kupferminc MJ. Mid-trimester severe intrauterine growth restriction is associated with a high prevalence of thrombophilia. BJOG. 2002; 109: 1373-6.
  • 22
    Luo X, Zhai S, Shi N, Li M, Cui S, Xu Y. The risk factors and neonatal outcomes of isolated single umbilical artery in singleton pregnancy: a meta-analysis. Sci Reports. 2017; 7: 7396.
  • 23
    Khoury M, Erickson J, Cordero J. Congenital malformations and intrauterine growth retardation: a population study. Pediatrics. 1988; 82: 830-90.
  • 24
    Rodger M, Paidas M, Claire M. Inherited thrombophilia and pregnancy complications revisited. Obs Gynecol. 2008; 112: 320-4.

Publication Dates

  • Publication in this collection
    12 Feb 2021
  • Date of issue
    2021

History

  • Received
    07 Nov 2019
  • Reviewed
    12 Nov 2019
  • Accepted
    15 Jan 2021
  • Published
    27 Oct 202020
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