Katherine E. Teague, Maurice K. Eggleston, Patrick E. Muffley, Robert B. Gherman
{"title":"Recurrent fetal cystic hygroma with normal chromosomes: Case report and review of the literature†","authors":"Katherine E. Teague, Maurice K. Eggleston, Patrick E. Muffley, Robert B. Gherman","doi":"10.1002/1520-6661(200011/12)9:6<366::AID-MFM1010>3.0.CO;2-E","DOIUrl":null,"url":null,"abstract":"<p>Recurrence of fetal cystic hygroma in subsequent pregnancies is extremely rare. A review of the literature to date revealed only two other reports of recurrence with normal fetal karyotypes documented in at least two of the affected pregnancies. At 11 weeks' gestation, the fetus of a 19-year-old gravida 3 para 0 was discovered to have a large cystic hygroma. Subsequent evaluation during the second trimester revealed increasing size of the septated nuchal mass and ascites. A 46,XX fetal karyotype was noted in her two prior pregnancies, both of which had also been complicated by the development of cystic hygroma and nonimmune hydrops. Cystic hygroma, associated with a normal karyotype, can be inherited as an autosomal recessive trait. J. Matern.-Fetal Med. 2000;9:366–369. © 2000 Wiley-Liss, Inc.</p>","PeriodicalId":79464,"journal":{"name":"The Journal of maternal-fetal medicine","volume":"9 6","pages":"366-369"},"PeriodicalIF":0.0000,"publicationDate":"2001-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1520-6661(200011/12)9:6<366::AID-MFM1010>3.0.CO;2-E","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of maternal-fetal medicine","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/1520-6661%28200011/12%299%3A6%3C366%3A%3AAID-MFM1010%3E3.0.CO%3B2-E","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
Abstract
Recurrence of fetal cystic hygroma in subsequent pregnancies is extremely rare. A review of the literature to date revealed only two other reports of recurrence with normal fetal karyotypes documented in at least two of the affected pregnancies. At 11 weeks' gestation, the fetus of a 19-year-old gravida 3 para 0 was discovered to have a large cystic hygroma. Subsequent evaluation during the second trimester revealed increasing size of the septated nuchal mass and ascites. A 46,XX fetal karyotype was noted in her two prior pregnancies, both of which had also been complicated by the development of cystic hygroma and nonimmune hydrops. Cystic hygroma, associated with a normal karyotype, can be inherited as an autosomal recessive trait. J. Matern.-Fetal Med. 2000;9:366–369. © 2000 Wiley-Liss, Inc.
染色体正常的复发性胎儿囊性水瘤:病例报告及文献复习†
胎儿囊性水肿在以后的妊娠中复发是极为罕见的。迄今为止的文献回顾显示,在至少两个受影响的妊娠中,只有另外两个报告的正常胎儿核型复发。在怀孕11周时,一名19岁的孕妇(第30段)的胎儿被发现有一个很大的囊性水瘤。在妊娠中期的后续评估显示分离的颈肿块和腹水的大小增加。在她之前的两次妊娠中发现胎儿核型为46,xx,这两次妊娠都伴有囊性水瘤和非免疫性水肿的发展。囊性水瘤与正常核型相关,可作为常染色体隐性遗传性状遗传。j . Matern。-胎儿医学,2000;9:36 - 369。©2000 Wiley-Liss, Inc。
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