先天性传染病足月儿胎盘的临床和形态学特征

A. V. Agafonova, V. V. Vasiliev, N. Rogozina
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引用次数: 0

摘要

材料和方法。对40例先天性感染性疾病患儿、10例新生儿窒息患儿和10例健康足月患儿的妊娠和分娩过程特点、出生时胎儿状况、胎盘组织形态学结论及CD15标志物的表达进行了分析。分析表明,缺乏可靠的临床和形态学标准的风险发展为先天性传染病。因此,各组患儿的母亲多数存在各种躯体病理:1组33例(82.5%),2组8例(80%),3组6例(60%)(p≥0.05)。各组患儿在胎龄、人体测量资料及Apgar量表评定上均具有统计学意义。组织学检查结果显示,两组患儿出生后发生炎症变化的频率基本相同:宫内感染患儿17例(42.5%),出生时窒息患儿4例(40%),健康患儿2例(20%)(p≥0.05)。同时免疫组化结果显示,先天性传染病患儿胎盘CD15表达水平明显高于健康患儿:先天性传染病患儿胎盘CD15表达系数为6.9±0.9,健康患儿为- 0.7±0.5,(p < 0.05)。利用免疫组织化学标志物CD15,可以在没有明显的产后感染性病变形态学征象的情况下预测新生儿先天性感染性疾病,并可用于形成危险群体实施感染性病理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and morphological characteristics of placentas of full-term infants with congenital infectious diseases
Materials and methods. The features of the course of pregnancy and childbirth, the condition of children at birth, histomorphological conclusions of placentas and the expression of the CD15 marker in the placentas of 40 children with congenital infectious diseases, 10 children with asphyxia at birth and 10 healthy full-term children were analyzed.Results. The analysis showed the absence of reliable clinical and morphological criteria for the risk of developing a congenital infectious disease. Thus, the majority of mothers of children of all comparison groups had various somatic pathology: 33 (82.5%) in group 1, 8 (80%) in group 2, 6 (60%) in group 3 (p ≥ 0.05) Children of all comparison groups were statistically comparable in gestational age, anthropometric data and assessment on the Apgar scale. During histological examination, inflammatory changes in the afterbirth in children of the compared groups were recorded with almost the same frequency: in 17 (42.5%) children with intrauterine infection, 4 (40%) with asphyxia at birth and 2 (20%) healthy children (p ≥ 0.05). At the same time, immunohistochemically, placentas of children with congenital infectious diseases were characterized by a significantly higher level of CD15 expression compared to placentas of healthy children: CD15 expression coefficient in placentas of children with congenital infectious diseases was 6.9 ± 0.9, in the group of healthy children — 0.7 ± 0.5, (p < 0.05).Conclusion. The use of the immunohistochemical marker CD15 makes it possible to predict congenital infectious disease in newborns in the absence of obvious morphological signs of an infectious lesion of the afterbirth, and can be used to form risk groups for the implementation of infectious pathology.
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