Stewart P A, Becker A E, Wladimiroff J W, Essed C E
J Am Coll Cardiol. 1984 Nov;4(5):1015-20. doi: 10.1016/s0735-1097(84)80065-0.
Complex congenital heart disease with suspected isomerism of the atria was diagnosed in two fetuses of 20 and 29 weeks' gestation using two-dimensional and M-mode scanning techniques. The first pregnancy was terminated at 21 weeks' gestation and stillbirth occurred at 31 weeks' gestation in the second pregnancy. At postmortem examination, a thoracoabdominal discordancy was found; the spleen was absent and the arrangement of the abdominal vessels was as anticipated for asplenia, but the thoracic situs revealed a bilateral right-sided arrangement with left isomerism of the atria. The heart, otherwise, showed complex abnormalities as anticipated for asplenia.
使用二维和M型扫描技术,在两名分别为孕20周和29周的胎儿中诊断出患有疑似心房异构的复杂先天性心脏病。第一例妊娠在孕21周时终止,第二例妊娠在孕31周时发生死产。尸检发现胸腹不协调;脾脏缺失,腹部血管排列符合无脾症的预期,但胸部位置显示双侧右侧排列伴心房左异构。心脏在其他方面则显示出符合无脾症预期的复杂异常。