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孤立性心包积液:胎儿染色体核型分析的指征?

Isolated pericardial effusion: an indication for fetal karyotyping?

作者信息

Sharland G, Lockhart S

机构信息

Department of Fetal Cardiology, Guy's and St. Thomas' Trust Hospital, London, UK.

出版信息

Ultrasound Obstet Gynecol. 1995 Jul;6(1):29-32. doi: 10.1046/j.1469-0705.1995.06010029.x.

Abstract

The outcome and associations of 35 consecutive cases of isolated pericardial effusion detected in the fetus are presented. In all cases included in the study, there was no evidence of a structural abnormality or a rhythm disturbance detectable antenatally. Karyotyping revealed that 26% of cases had trisomy 21 and 31% of the total had some form of chromosomal anomaly. Our study shows that the outlook for isolated pericardial effusion is good. However, there is a high incidence of associated karyotypic anomalies, in particular trisomy 21. Fetal karyotyping is therefore recommended in these cases.

摘要

本文报告了连续检测出的35例胎儿孤立性心包积液的结果及相关情况。在本研究纳入的所有病例中,产前均未发现结构异常或节律紊乱的证据。染色体核型分析显示,26%的病例为21三体,占总数31%的病例存在某种形式的染色体异常。我们的研究表明,孤立性心包积液的预后良好。然而,相关染色体核型异常的发生率很高,尤其是21三体。因此,建议对这些病例进行胎儿染色体核型分析。

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