Thomas D, Lefebvre C, Gossens A, Heimann H, De Hoe F, Claes J P, La Haye M
Service de Gynécologie-Obstétrique, Maternité de l'Hôpital d'Ixelles, Bruxelles, Belgique.
J Gynecol Obstet Biol Reprod (Paris). 1988;17(4):501-6.
Two cases of pulmonary cystic adenomatoid malformation are presented. The first case presented with bilateral pulmonary cystic involvement associated with oligoamnios and feto-placental anasarca. A peculiar feature of this case was the elevated level of alphafetoprotein in the amniotic fluid. In the second case, the pulmonary involvement was limited to one lobe. There was coexistent aplasia of the diaphragm. Premature rupture of the amniotic membranes necessitated a therapeutic abortion at 21 weeks of pregnancy. In connection with these two cases, a discussion based on the data in the literature.
本文报告了两例肺囊性腺瘤样畸形病例。第一例表现为双侧肺囊肿累及,伴有羊水过少和胎儿-胎盘水肿。该病例的一个特殊特征是羊水甲胎蛋白水平升高。第二例中,肺部受累局限于一个肺叶。同时存在膈肌发育不全。胎膜早破导致在妊娠21周时进行了治疗性流产。结合这两例病例,根据文献数据进行了讨论。