Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul 110-744, Korea.
Korean J Radiol. 2010 Jan-Feb;11(1):119-22. doi: 10.3348/kjr.2010.11.1.119. Epub 2009 Dec 28.
We report a case of bilateral pulmonary agenesis (BPA), which was suspected during a prenatal US examination and diagnosed by fetal magnetic resonance imaging (MRI). BPA is an extremely rare congenital anomaly and, although many fetal structural defects can be detected with a high degree of confidence after introducing high-resolution US, the prenatal diagnosis of BPA remains problematic. Other thoracic abnormalities, such as a congenital diaphragmatic hernia, congenital cystic adenomatoid malformation, and pulmonary sequestration, should be excluded from the list of possible diagnoses before coming to the conclusion of BPA, because BPA is absolutely incompatible with extrauterine life, and an accurate internal diagnosis can prevent a futile intervention from being performed.
我们报告了一例双侧肺发育不全(BPA)病例,该病例在产前超声检查中被怀疑,并通过胎儿磁共振成像(MRI)诊断。BPA 是一种极其罕见的先天性异常,尽管在引入高分辨率超声后,许多胎儿结构缺陷都可以高度置信地检测到,但 BPA 的产前诊断仍然存在问题。其他胸部异常,如先天性膈疝、先天性囊性腺瘤样畸形和肺隔离症,应在得出 BPA 的结论之前从可能的诊断列表中排除,因为 BPA 与宫外生活完全不兼容,准确的内部诊断可以防止进行无益的干预。