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[胎儿颈部水囊瘤的超声检测]

[Sonographic detection of hygroma colli in the fetus].

作者信息

Friese K, Merz E

机构信息

Universitätsfrauenklinik Mainz.

出版信息

Ultraschall Med. 1989 Feb;10(1):25-8. doi: 10.1055/s-2007-1005956.

Abstract

Foetal cystic hygroma is a congenital malformation of the lymphatic systems. Ten cases of foetal cystic hygroma were diagnosed prenatally during the second trimester, in a period of two years, at Ultrasound Unit of the Department of Obstetrics and Gynaecology of the University of Mainz, West Germany. Six foetuses had Turner's syndrome, one had a 47 X + 21 karyotype, two foetuses were cytogenetically normal and in one case tue chromosome cultures failed. Sonographic findings are demonstrated and compared to autopsy results. In addition, clinical management of foetuses with cystic hygroma are discussed.

摘要

胎儿颈部水囊瘤是一种淋巴管的先天性畸形。在两年时间里,德国美因茨大学妇产科超声科在孕中期产前诊断出10例胎儿颈部水囊瘤。6例胎儿患有特纳综合征,1例核型为47,XX,+21,2例胎儿细胞遗传学检查正常,1例染色体培养失败。展示了超声检查结果并与尸检结果进行了比较。此外,还讨论了患有颈部水囊瘤胎儿的临床处理。

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[Sonographic detection of hygroma colli in the fetus].[胎儿颈部水囊瘤的超声检测]
Ultraschall Med. 1989 Feb;10(1):25-8. doi: 10.1055/s-2007-1005956.
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Fetal cystic hygroma colli: antenatal diagnosis, significance, and management.
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