胎盘病理与早发性胎儿生长受限之间的关系:一项系统综述。

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2025-01-01 Epub Date: 2024-12-11 DOI:10.1080/15513815.2024.2437642
Beatriz Pinheiro, Inês Sarmento-Gonçalves, Carla Ramalho
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引用次数: 0

摘要

目的:胎儿生长受限(FGR)被定义为胎儿未能实现其遗传决定的生长潜能。我们的目的是比较早发性胎儿生长受限和晚发性FGR的胎盘病变。方法:我们根据PRISMA指南进行了系统评价。观察性研究,仅在单胎妊娠中,评估早期与晚发性FGR中胎儿生长受限与胎盘病变之间的关系。结果:我们纳入了6篇文章。所有研究均显示,与迟发性FGR组相比,早发性FGR组的母体血管灌注不良(MVM)病变发生率更高。五篇文章报道早发性FGR常与先兆子痫相关。结论:本综述显示早发性FGR病例与特定的胎盘组织病理学相关,如母体血管灌注不良病变。胎盘组织病理学检查对于更好地了解FGR的病理生理具有重要意义。
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Association Between Placental Pathology and Early-Onset Fetal Growth Restriction: A Systematic Review.

Objective: Fetal growth restriction (FGR) is defined as the failure of the fetus to achieve its genetically determined growth potential. Our aim is to compare the placental lesions present in early-onset fetal growth restriction with that of late-onset FGR. Methods: We performed a systematic review according to the PRISMA guideline. Observational studies, only in singleton pregnancies, evaluating the association between fetal growth restriction and placental lesions in early- versus late-onset FGR were included. Results: We included six articles. All studies showed a higher rate of maternal vascular malperfusion (MVM) lesions in the early-onset FGR groups when compared to late-onset ones. Five articles reported that early-onset FGR is often associated with pre-eclampsia. Conclusion: This review shows that early-onset FGR cases are associated with specific placental histopathology, such as maternal vascular malperfusion lesions. Placental histopathological examination is important to better understand the pathophysiology of FGR.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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