Correia-Pinto Jorge, Gonzaga Sílvia, Huang Yadi, Rottier Robbert
Surgical Sciences Research Domain, Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal.
Semin Pediatr Surg. 2010 Aug;19(3):171-9. doi: 10.1053/j.sempedsurg.2010.03.003.
Congenital lung lesions comprise a broad spectrum of rare but clinically significant developmental abnormalities, including congenital cystic adenomatoid malformation, bronchopulmonary sequestrations, congenital lobar emphysema, and bronchogenic cysts, which are commonly surgically treated. Although the terms congenital cystic adenomatoid malformation, bronchopulmonary sequestrations, congenital lobar emphysema, and bronchogenic cysts are entrenched in clinical usage and comfortably correspond to rigid pathologic definitions, there is a considerable overlap in the findings. Disregarding the controversy about lesion nomenclature and classification, it is widely accepted that congenital lung lesions result from perturbations in lung and airway embryogenesis. It is generally accepted that both place (level in the tracheobronchial tree) and timing (gestational age) of the embryologic insult correlates with the type of lesion and histopathology that is manifested. The objective of this review is to briefly review normal lung development and to analyze the known molecular mechanisms underlying those diseases.
先天性肺部病变包括一系列广泛的罕见但具有临床意义的发育异常,包括先天性囊性腺瘤样畸形、肺隔离症、先天性大叶性肺气肿和支气管囊肿,这些疾病通常采用手术治疗。尽管先天性囊性腺瘤样畸形、肺隔离症、先天性大叶性肺气肿和支气管囊肿这些术语在临床应用中已根深蒂固,并且与严格的病理学定义相符,但在检查结果上存在相当大的重叠。尽管关于病变命名和分类存在争议,但人们普遍认为先天性肺部病变是由肺和气道胚胎发生过程中的扰动引起的。人们普遍认为,胚胎损伤的部位(气管支气管树中的水平)和时间(胎龄)都与所表现出的病变类型和组织病理学相关。本综述的目的是简要回顾正常肺发育,并分析这些疾病潜在的已知分子机制。