Prenatal diagnosis of abdominal cystic hygroma

1988 ◽  
Vol 8 (6) ◽  
pp. 405-409 ◽  
Author(s):  
Karen J. Kozlowski ◽  
Cynthia N. Frazier ◽  
J. Gerald Quirk
Keyword(s):  
Prenatal Diagnosis ◽  
Cystic Hygroma

scholarly journals PRENATAL DIAGNOSIS OF JACOBSEN SYNDROME WITH CYSTIC HYGROMA

2020 ◽  
Vol 07 (01) ◽  
pp. 45-46
Author(s):  
Toshifumi Suzuki ◽  
Takashi Hayashi ◽  
Atsuo Itakura
Keyword(s):  
Prenatal Diagnosis ◽  
Cystic Hygroma ◽  
Jacobsen Syndrome

Prenatal diagnosis of nuchal cystic hygroma

1991 ◽  
Vol 64 (765) ◽  
pp. 802-807 ◽  
Author(s):  
A. M. MacLeod ◽  
J. M. McHugo
Keyword(s):  
Prenatal Diagnosis ◽  
Cystic Hygroma

Prenatal diagnosis of recurrence of cystic hygroma with normal chromosomes

1984 ◽  
Vol 4 (5) ◽  
pp. 383-386 ◽  
Author(s):  
Bruno Dallapiccola ◽  
Leopoldo Zelante ◽  
Gianni Perla ◽  
Giuseppe Villani
Keyword(s):  
Prenatal Diagnosis ◽  
Cystic Hygroma

Cystic hygroma colli: Perinatal outcome after prenatal diagnosis

1991 ◽  
Vol 19 (6) ◽  
pp. 449-454 ◽  
Author(s):  
Sabine Droste ◽  
Susan K. Hendricks ◽  
Holly v. Alfrey ◽  
and Lawrence A. Mack
Keyword(s):  
Prenatal Diagnosis ◽  
Perinatal Outcome ◽  
Cystic Hygroma

scholarly journals Diagnostic value of systematic ultrasonography for trisomy 18 syndrome in fetuses before 16 weeks gestation

2021 ◽  
Author(s):  
Jie Zhou ◽  
Xiaohui Dai ◽  
Hanmin Liu ◽  
Yiping Li ◽  
Ling Luo ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Birth Rate ◽  
Nuchal Translucency ◽  
Diagnostic Value ◽  
Cystic Hygroma ◽  
Trisomy 18 ◽  
Ductus Venosus ◽  
Research Subjects ◽  
Fetal Ultrasonography ◽  
Cardiac Defects

Abstract Purpose To explore the diagnostic value of systematic fetal ultrasonography for trisomy 18 (T18) syndrome before 16 weeks gestation. Methods A total of 12 fetuses with T18 were selected as research subjects and their nuchal translucency (NT) screening and fetal systematic ultrasonographic images acquired at 11–15 weeks were retrospectively analyzed. Results In the 12 fetuses’ NT screening, ten fetuses showed NT thickening, one showed nuchal cystic hygroma, four showed reversed a-wave ductus venosus flow, and three showed omphalocele. The most common anomalies on the systematic ultrasonography before 16 weeks gestation were cardiac defects (12/12, 100%), omphalocele (4/12, 33.3%), limb anomalies (5/12, 41.7%), and facial anomalies (3/12, 25.0%). Seven of the 12 fetuses had multiple structural malformations: three had two structural malformations (25.0%), three had three structural malformations (25.0%), and one had four structural malformations (8.3%). Conclusion Systematic fetal ultrasonography before 16 weeks gestation can detect most of the structural malformations of T18, effectively shortening the prenatal diagnosis time. It is therefore of great importance for reducing the birth rate of children with T18 and minimizing the physical and mental damage to mothers and their families.

Ebstein’s anomaly: a multicenter analysis of 56 prenatal diagnosis cases

2018 ◽  
Author(s):  
M.V. Medvedev , I.V. Komarova , E.V. Potolova et all
Keyword(s):  
Prenatal Diagnosis ◽  
Tricuspid Valve ◽  
Gestational Age ◽  
Heart Diseases ◽  
Cystic Hygroma ◽  
Intrauterine Fetal Death ◽  
Ebstein’S Anomaly ◽  
Ebstein Anomaly ◽  
Ebstein's Anomaly ◽  
Multicenter Analysis

Retrospectively, 56 cases of prenatal diagnosis of Ebstein’s anomaly (EA) were analysed. The mean gestational age at diagnosis was 24.3 weeks (range: 11+6–39 weeks). 14.8% cases were diagnosed until 14 weeks, 46.3% — before 22 weeks. The successfulness of prenatal ultrasound diagnosis of EA at 11–14 weeks of gestation is equal to 26.7%. 24 (42.8%) pregnant women opted for termination of pregnancy, intrauterine fetal death occurred in 4 cases (7.1%), 23 (41.1%) were born alive, in 5 cases the outcomes were not available. 8 liveborn infants were died at the neonatal age (34.8%), 2 — until 1 year (8.7%). 13 children were alive during the period of monitoring 3 months — 9 years old (56.5%), from them 5 children were get operated (38.5%). In all cases EA successful diagnostics was based on the detection of tricuspid valve displacement and tricuspid regurgitation. The cardiac arrhythmia was not detected. 26 cases (46.4%) were isolated without accompanying cardiac pathology, and that was 1.5 times more frequently for alive infants, than for died. Among the accompanying congenital heart diseases pulmonary artery obstructions were dominated — 20 cases (66.7%) and ventricular septal defects — 14 cases (46.7%). Accompanying congenital disorders were detected at 6 cases (10.7%), among 6. Алтынник Н.А. Пренатальная ультразвуковая диагностика аномалии Эбштейна до 12 недель беременности. Пренат. Диагн. 2018; 17 (2): 152–154. 7. Jadaon J.E, Haddad S., Mukary M., Ben-Shlomo I., BenAmi M. Evaluation of normal fetal atrio-ventricular septum dimensions during pregnancy. Prenat. Diagn. 2011; 31 (2): 167–170. 8. Anderson H.N., Dearani J.A., Said S.M., Norris M.D., Pundi K.N., Miller A.R., Cetta M.L., Eidem B.W., O'Leary P.W., Cetta F. Cone reconstruction in children with Ebstein anomaly: the Mayo Clinic experience. Congenit. Heart Dis. 2014; 9 (3): 266–271. 9. Болсуновский В.А. и соавт. Аномалия Эбштейна: операция конусной реконструкции — первый опыт анатомической коррекции. Лечащий врач. 2017, № 1. https:// www.Ivrach.ru 10. Медведев М.В., Юдина Е.В., Левченко В.А. и др. Перинатальные исходы при врожденных пороках развития. IХ. Аномалия Эбштейна. Пренат. Диагн. 2003; 2 (4): 288–292. 11. Медведев М.В. Эхокардиография плода. М.: Реальное Время, 2000; 144. 12. Комарова И.В., Гартунг Т.С., Данкова О.В., Большакова Т.Г., Чикаленко С.Ю., Винокурова Е.А., Кукарская И.И. Пренатальная диагностика сочетания аномалии Эбштейна и синдрома Дауна: обзор литературы и собственное наблюдение. Пренат. Диагн. 2018; 17 (1): 42–47. 13. Gottschalk I., Gottschalk L., Stressig R., Ritgen J., Herberg U., Breuer J., Oberhoffer R., Willruth A., Strizek B., Geipel A., Gembruch U., Berg C. Ebstein's Anomaly of the Tricuspid Valve in the Fetus – A Multicenter Experience. Ultraschall Med. 2017; 38 (4): 427–436. ПРЕНАТАЛЬНАЯ ДИАГНОСТИКА Аномалия Эбштейна: мультицентровой анализ 317 56 случаев пренатальной диагностики 2018 Т 17 № 4; 310-317 them — 3 cases of cystic hygroma, 2 — corpus callosum agenesis, 1 — trisomy 21. At 7 cases were detected nonimmune hydrops (12.5%). The characteristics of cardiomegaly – cardiothoracic diameter ratio (CDR) and cardiothoracic square ratio (CSR) — trend upward with increasing gestational age and these factors were worse in the group of fetus died than alive. CDR and CSR as an isolated prognostic markers were effective in prediction of infant mortality with sensitivity about 100% upon  0.75 for CDR and  0.4 for CSR.

Early Prenatal Diagnosis of Cystic Hygroma by Real‐Time Ultrasound

1985 ◽  
Vol 13 (9) ◽  
pp. 655-658 ◽  
Author(s):  
Niek Exalto ◽  
Rieteke M. Zalen ◽  
Wilma J. A. Brandenburg
Keyword(s):  
Prenatal Diagnosis ◽  
Real Time ◽  
Cystic Hygroma
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