Moerman P, Fryns J P, Vandenberghe K, Devlieger H, Lauweryns J M
Department of Pathology I, Katholieke Universiteit, Leuven, Belgium.
Histopathology. 1992 Oct;21(4):315-21. doi: 10.1111/j.1365-2559.1992.tb00401.x.
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.
先天性囊性腺瘤样畸形是一种罕见的肺发育异常。在大多数早期报道的病例中,支气管树的解剖结构记录不佳。我们描述了四例尸检后的研究病例。尸检支气管造影或连续显微镜检查显示,每例均存在节段性支气管缺如或闭锁。我们的观察结果提供了进一步的证据,表明支气管闭锁是导致先天性囊性腺瘤样畸形发生的主要缺陷。病变的形态,即畸形的类型,取决于发育异常的肺组织在闭锁节段以外的生长范围。支气管闭锁的病因可能是异质性的,可能代表原发性畸形,也可能是血管破坏的结果。