PATHOGENESIS OF CONGENITAL CYSTIC ADENOMATOID MALFORMATION OF THE LUNG

被引:71
作者
MOERMAN, P
FRYNS, JP
VANDENBERGHE, K
DEVLIEGER, H
LAUWERYNS, JM
机构
[1] CATHOLIC UNIV LEUVEN,DEPT PAEDIAT,B-3000 LOUVAIN,BELGIUM
[2] CATHOLIC UNIV LEUVEN,DEPT PATHOL 1,B-3000 LOUVAIN,BELGIUM
[3] CATHOLIC UNIV LEUVEN,DEPT HUMAN BIOL,DIV HUMAN GENET,B-3000 LOUVAIN,BELGIUM
[4] CATHOLIC UNIV LEUVEN,DEPT OBSTET & GYNECOL,B-3000 LOUVAIN,BELGIUM
关键词
BRONCHIAL ATRESIA; CONGENITAL CYSTIC ADENOMATOID MALFORMATION; PERINATAL AUTOPSY;
D O I
10.1111/j.1365-2559.1992.tb00401.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Congenital cystic adenomatoid malformation is a rare developmental abnormality of the lung. In most earlier reported cases, the anatomy of the bronchial tree was poorly documented. We describe four cases studied following autopsy. Post-mortem bronchography or serial microscopical examination showed segmental bronchial absence or atresia in each of them. Our observations provide further evidence pointing to bronchial atresia as being the primary defect leading to the development of congenital cystic adenomatoid malformation. The morphology of the lesion, i.e. the type of malformation, is determined by the extent of dysplastic lung growth beyond the atretic segment. The aetiology of the bronchial atresia is probably heterogeneous and may either represent a primary malformation, or be the result of vascular disruption.
引用
收藏
页码:315 / 321
页数:7
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