首页    期刊浏览 2024年12月14日 星期六
登录注册

文章基本信息

  • 标题:Ascitis fetal masiva idiopática aislada
  • 本地全文:下载
  • 作者:Yolimar Navarro Briceño ; Joel Santos Bolívar ; Eduardo Reyna Villasmil
  • 期刊名称:Avances en Biomedicina
  • 印刷版ISSN:2244-7881
  • 出版年度:2016
  • 卷号:5
  • 期号:2
  • 页码:99-103
  • 语种:English
  • 出版社:Avances en Biomedicina
  • 摘要:Fetal ascites is commonly associated with gastrointestinal and urinary malformation, anemia, infection and chromosomal anomalies. Idiopathic massive fetal ascites is rare. We report a case of a 33-year-old pregnant woman referred at 17 weeks after significant ascites were detected in the absence of structural anomalies. Fetal cardiac scan were normal and viral diagnostic assay were negative. By 28 weeks massive ascites was detected with no other signs of fetal hydrops. Fetal middle cerebral artery peak systolic velocity was elevated. Umbilical artery Doppler, fetal growth and amniotic fluid volume were normal. Fetal echocardiogram was normal. Amniocentesis was done with normal karyotype results. Despite the persistence of massive ascites, serial ultrasound scans showed reassuringly normal growth and umbilical artery Doppler with high values of middle cerebral artery peak systolic velocity. At 33 weeks gestation an emergency caesarean section was done due to acute fetal distress. A female newborn was obtained with normal values of hemoglobin at birth. Liver, bladder and hepato-portal vascular flow were normal. Ascites resolved completely by day 8 and the baby was discharged after 15 days.
  • 关键词:Idiopathic fetal ascites, Fetal diseases, Normal karyotype;Ascitis fetal idiopática;enfermedades fetales;cariotipo normal
国家哲学社会科学文献中心版权所有