The Potential Role of Placenta Morphological, Cytogenetic and Histological Findings in Fetal Phenotype Modeling: A Case Report with Unanswered Questions
Case studies
Estere Strautmane
Riga Stradiņš University image/svg+xml
https://orcid.org/0009-0003-7608-2073
Liene Korņejeva
Riga Maternity Hospital
Dzintra Ločmele
Riga Maternity Hospital; Medical Genetics and Prenatal Diagnostics Clinic, Children's Clinical University Hospital, Riga
Marta Riekstiņa
Children’s Clinical University Hospital, Department of Pathology, Riga
Diāna Bokučava
Riga Maternity Hospital
Natālija Vedmedovska
Riga Stradins University, Department of Obstetrics and Gynecology; Riga Maternity Hospital
https://orcid.org/0000-0003-2343-2693
Published 2025-02-21
https://doi.org/10.15388/Amed.2025.32.1.8
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Keywords

fetal growth restriction
small-for-gestational-age
chorionic villus sampling
intraplacental hemorrhage
intervillous thrombi
perivillous fibrin deposition

How to Cite

1.
Strautmane E, Korņejeva L, Ločmele D, Riekstiņa M, Bokučava D, Vedmedovska N. The Potential Role of Placenta Morphological, Cytogenetic and Histological Findings in Fetal Phenotype Modeling: A Case Report with Unanswered Questions. AML [Internet]. 2025 Feb. 21 [cited 2025 Mar. 9];32(1):8. Available from: https://www.journals.vu.lt/AML/article/view/37316

Abstract

Placental abnormalities significantly contribute to fetal mortality. Maternal vascular underperfusion emerges as the prevailing diagnosis. At the same time, genomic alterations within the placenta might play a role in the development of placental dysfunction. We present a case report of a 24-year-old primigravida with an uneventful medical history, admitted at 21 weeks and 2 days gestation. Despite a low risk for typical trisomies, a high risk for preeclampsia and fetal growth restriction (FGR) was recognized in the first trimester. Anhydramnios, abnormal placental morphology, retrochorial and retromembranous hematomas were observed, prompting the termination of pregnancy (TOP). Histological examination revealed multiple placental abnormalities, while the fetus displayed normal anatomy and phenotype. Discussion encompasses the varied manifestations of histopathological findings, and potential associations with adverse pregnancy outcomes. Our case underscores the importance of meticulous evaluation and multidisciplinary collaboration in managing pregnancies with placental anomalies. Further research is crucial to discern the intricate relationship between placental cytogenetics, morphology, and pregnancy outcomes, thus facilitating better clinical management and counseling strategies.

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