胎儿心内超声灶的研究:与组织病理学相关性探讨回声性的可能病因

S. Philip, S. Philip, P. Vaideeswar, U. Singh
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引用次数: 0

摘要

目的:本研究的目的是确定心脏内回声灶(ICEF)的频率、位置和回声范围,并探讨ICEF的可能病因。材料与方法:回顾性研究2010年至2020年2445例妊娠中晚期胎儿心脏超声检查病例,以排除先天性心脏病为目标,对ICEF进行详细评价和分析。对64例ICEF患儿进行了进一步的产后随访,直至7岁,观察其自然病程。对一例妊娠19周的胎儿尸检进行了组织病理学检查,以进一步研究两者之间的相关性。结果:胎儿心脏超声中出现ICEF 323例(13.2%)(95%可信区间11.9 ~ 14.6)。大多数ICEF(96%)位于左心室腔,其次是两个心室(3%),其余位于右心室,均位于乳头肌内。在对66例产后病例的随访中,97%的ICEF在5岁时消退。只有两例报告有先天性心脏病。在任何情况下均无染色体异常。一例胎儿心脏标本的组织病理学显示乳头肌顶端有黏液瘤变性。结论:单次ICEF在左心室发生率高得多,且均位于前乳头肌的上三分之一。随着胎龄的增加,ICEF可以在子宫内消除,并在出生后1-7岁时进一步完全消除。回声变异性可能是粘液瘤组织向纤维化或微钙化转变的一部分。在本研究中,ICEF与先天性心脏病或染色体没有特别的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Study on Fetal Intracardiac Echogenic Foci: Pondering Possible Etiology of Echogenicity with Histopathology Correlation
Objective: The objective of this study is to determine the frequency, location, and delineation of the echogenicity of intracardiac echogenic foci (ICEF) and to ponder the possible etiology of ICEF. Materials and Methods: Retrospective study of 2445 referred cases in second and third trimester for fetal cardiac ultrasound scan from 2010 to 2020, targeted for ruling out congenital heart disease were evaluated and analyzed in detail for ICEF. Further postnatal follow-up was done in 64 cases of ICEF till 7 years of age to see the natural course. Histopathology was performed from one case of fetal autopsy at 19 weeks of gestation for further correlation. Results: Among the fetal cardiac ultrasound cases, 323 (13.2%) showed ICEF (95% confidence interval 11.9–14.6). Majority of these ICEF (96%) were in the left ventricular cavity, and then both ventricles (3%) and remaining in right ventricle and all were located within the papillary muscles. On follow-up of 66 postnatal cases, ICEF had resolved in 97% by 5 years of age. Only two cases reported to have congenital heart disease. No chromosomal anomalies was associated in any case. Histopathology of fetal heart specimen in one case revealed myxomatous degeneration at the apices of the papillary muscle. Conclusion: Frequency of single ICEF is much higher in the left ventricle, and it is invariably located within the upper third of the anterior papillary muscle in such cases. As the gestational age advances, ICEF can resolve in utero, and further complete resolution is seen by 1–7 years of postnatal life. Variability in the echogenicity could be part of transformation of myxomatous tissues to fibrosis or microcalcification. In this study, ICEF have no particular association with congenital heart disease or chromosomal association.
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