Evans J A
Department of Human Genetics, University of Manitoba, Winnipeg, Canada.
Am J Med Genet. 1990 Jan;35(1):46-54. doi: 10.1002/ajmg.1320350109.
In an investigation of malformation associations in consecutive perinatal autopsies, 4 infants were identified as having a displaced or supernumerary bronchus. Each had a different type of bronchial abnormality and 3 had congenital heart defects and other malformations. Review of the literature found 38 other cases of aberrant bronchi with additional defects, especially cardiovascular or costovertebral anomalies. Structural cardiac defects were more common in patients with super-numerary tracheal bronchi (67%) than in those with displaced tracheal bronchi (27%) or bronchoesophageal connections (23%). There was also a strong negative association (P = 0.01) of cardiovascular and costovertebral defects unless multiple anomalies were present. The combinations of anomalies seen appear to reflect relatively specific developmental field defects affected both by the spatial relationships of organs near the developing foregut and by temporal sequence. Recognition of these patterns has clinical and embryological importance. Aberrant bronchi should be considered when children with cardiac defects or multiple anomalies such as the VACTERL association have unexplained respiratory symptoms and surgeons planning to treat such bronchial abnormalities should be aware of the high frequency of abnormal vessels in these cases.
在一项对连续围产期尸检中畸形关联的调查中,4名婴儿被确定存在移位或额外支气管。每名婴儿都有不同类型的支气管异常,其中3名有先天性心脏缺陷和其他畸形。文献回顾发现另外38例异常支气管合并其他缺陷的病例,尤其是心血管或肋椎骨异常。结构性心脏缺陷在有额外气管支气管的患者中(67%)比在有移位气管支气管的患者中(27%)或支气管食管连接的患者中(23%)更常见。除非存在多种异常,心血管和肋椎骨缺陷之间也存在强烈的负相关(P = 0.01)。所观察到的异常组合似乎反映了受发育中的前肠附近器官的空间关系和时间顺序影响的相对特定的发育领域缺陷。认识这些模式具有临床和胚胎学意义。当患有心脏缺陷或多种异常(如VACTERL综合征)的儿童出现无法解释的呼吸道症状时,应考虑存在异常支气管,并且计划治疗此类支气管异常的外科医生应意识到这些病例中异常血管的高发生率。