Strife J L, Towbin R B, Francis P, Kuhn J P
Radiology. 1981 Dec;141(3):675-7. doi: 10.1148/radiology.141.3.7302222.
Chest radiographs obtained at birth in two neonates with absent pulmonary valve and tetralogy of Fallot demonstrated asymmetrical lung aeration. This finding was attributed to delay in resorption of fetal lung fluid. It is postulated that in the initial hours of life, the dilated pulmonary artery compressed the bronchus and delayed egress of fetal lung fluid. Over a 24-hour interval, the fluid was resorbed, resulting in the more typical pattern of hyperinflated lung and markedly dilated pulmonary artery. These cases are presumably the first of their kind to be reported.
在两名患有肺动脉瓣缺如和法洛四联症的新生儿出生时所拍摄的胸部X光片显示肺部通气不对称。这一发现归因于胎儿肺液吸收延迟。据推测，在生命的最初几个小时，扩张的肺动脉压迫支气管并延迟了胎儿肺液的排出。在24小时内，液体被吸收，从而导致更典型的肺过度充气和肺动脉明显扩张的模式。这些病例大概是同类病例中首次被报道。
