Chao A, Monoson R F
Department of Obstetrics and Gynecology, University of California, Los Angeles.
J Reprod Med. 1990 Jun;35(6):655-7.
A pulmonary cystic adenomatoid malformation with evolving fetal hydrops was diagnosed in the early third trimester. Serial needle aspiration succeeded in resolving the hydrops; however, despite lobectomy the neonate died of microscopic contralateral disease undetected on ultrasound. The extent and nature of the underlying anomaly may limit the efficacy of fetal therapy for cystic adenomatoid malformation.
孕晚期早期诊断出一例伴有胎儿水肿进展的肺囊性腺瘤样畸形。连续穿刺抽吸成功解决了水肿问题；然而，尽管进行了肺叶切除术，新生儿仍死于超声未检测到的微小对侧病变。潜在异常的范围和性质可能会限制胎儿治疗肺囊性腺瘤样畸形的疗效。
