{"title":"[Prenatal diagnosis of fetal nuchal cystic hygroma in 22 cases].","authors":"J Du, L Qu, S Guo","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the early diagnosis and prognosis of fetal nuchal cystic hygroma.</p><p><strong>Methods: </strong>72 cases of fetal nuchal cystic hygroma diagnosed in uterus were analyzed retrospectively.</p><p><strong>Results: </strong>Most of the cases were diagnosed by B ultrasound between 15-26 gestational weeks. 55.9% the multipara had abnormal pregnant history, and 40% (4/10) of fetuses with karyotype performed had chrosome abnormality. Except for fetal deaths and induced abortions, 3 cases had term deliveries: one neonatal death, one was born with hygroma of 5.9 cm x 3.7 cm and transferred for surgery, and the other one with hygroma disappeared at the 37th week and baby was born at 40 week with normal appearance.</p><p><strong>Conclusions: </strong>This disease is one of common fetal morphological abnormalities. Few may recover spontaneously but most have poor outcomes.</p>","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"32 7","pages":"425-7"},"PeriodicalIF":0.0000,"publicationDate":"1997-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华妇产科杂志","FirstCategoryId":"3","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To investigate the early diagnosis and prognosis of fetal nuchal cystic hygroma.
Methods: 72 cases of fetal nuchal cystic hygroma diagnosed in uterus were analyzed retrospectively.
Results: Most of the cases were diagnosed by B ultrasound between 15-26 gestational weeks. 55.9% the multipara had abnormal pregnant history, and 40% (4/10) of fetuses with karyotype performed had chrosome abnormality. Except for fetal deaths and induced abortions, 3 cases had term deliveries: one neonatal death, one was born with hygroma of 5.9 cm x 3.7 cm and transferred for surgery, and the other one with hygroma disappeared at the 37th week and baby was born at 40 week with normal appearance.
Conclusions: This disease is one of common fetal morphological abnormalities. Few may recover spontaneously but most have poor outcomes.
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