Wagenvoort C A, Zondervan P E
Department of Pathology, Erasmus University Rotterdam, The Netherlands.
Pediatr Pathol. 1991 Mar-Apr;11(2):311-20. doi: 10.3109/15513819109064768.
A left lower polyalveolar lobe in a 28-day-old infant and a right lung with congenital cystic adenomatoid malformation type II in a 17-day-old infant are described. The adenomatoid malformation involved all lobes, but the lower lobe appeared to be mostly replaced by a polyalveolar area, a complication hitherto undescribed. The pronounced increase in number of alveoli in both cases was established by two different morphometric methods and was compared with three normal controls of the same age. The simultaneous occurrence of polyalveolar lobe and congenital cystic adenomatoid malformation type II in the same lung suggests a causal relation between both anomalies. In the grossly abnormal lung tissue of an adenomatoid malformation, polyalveolar areas can easily be overlooked.
描述了一名28日龄婴儿的左下多肺泡叶和一名17日龄婴儿的右肺先天性II型囊性腺瘤样畸形。腺瘤样畸形累及所有肺叶,但下叶似乎大部分被多肺泡区域取代,这是一种迄今未描述的并发症。通过两种不同的形态测量方法确定了两例中肺泡数量的显著增加,并与三个相同年龄的正常对照进行了比较。同一肺中多肺泡叶和先天性II型囊性腺瘤样畸形的同时出现表明这两种异常之间存在因果关系。在腺瘤样畸形的严重异常肺组织中,多肺泡区域很容易被忽视。