Clinicopathological and molecular genetic features of confined placental mosaicism
10.3760/cma.j.cn112151-20240318-00169
- VernacularTitle:限制性胎盘嵌合临床病理及分子遗传学分析
- Author:
Aichun WANG
1
;
Junling XIE
;
Jianjiang ZHU
;
Yuemei ZHANG
;
Muyu ZHANG
;
Hong QI
;
Yiqun GU
Author Information
1. 北京市海淀区妇幼保健院病理科，北京 100195
- Keywords:
Placenta;
Fetal development;
Pregnancy outcome;
Confined placental mosaicism
- From:
Chinese Journal of Pathology
2024;53(7):697-701
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To investigate the clinicopathological and genetic features of confined placental mosaicism (CPM) and its effect on fetal intrauterine growth.Methods:Fourteen CPM cases of Haidian Maternal and Children Health Hospital were collected from May 2018 to March 2022. Clinicopathological examination on placental specimens and molecular genetic analysis were performed.Results:The age of the parturient women ranged from 27 to 34 years, with an average age of (30.0±3.54) years. The gestational weeks ranged from 35 +1 to 41 +2 weeks. There were 4 premature births and 10 term births, among which 6 were female and 8 were male fetuses. Nine cases (9/14) had adverse pregnancy outcomes, including 7 cases of fetal growth restriction. The weight of CPM placenta decreased, with 6 cases below the 10th percentile of weight standards and 5 cases between the 10th and 25th percentile. All 14 CPM placental specimens showed morphological changes of perfusion dysfunction to varying degrees, with mainly placental-maternal vascular malperfusion followed by placental-fetal vascular malperfusion. The mosaic chromosomes in different CPM cases varied, with 16-trisomy/monosomy mosaicism being the most common followed by 7-trisomy and 21-trisomy/monosomy mosaicism. The mosaic proportion was unequal in different parts of the same CPM placenta, with the mosaic proportion of umbilical cord, fetal membranes, fetal surface, maternal surface, and edge ranging from 1% to 70%. Conclusions:The mosaic chromosomes in different CPM cases vary, and the mosaic proportion is unequal in different parts of the same CPM placenta. The pathological morphology is mainly manifested as perfusion dysfunction, which can lead to adverse pregnancy outcomes such as fetal growth restriction and preterm birth.
