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Congenital lung lesions--underlying molecular mechanisms.

机译:先天性肺部病变-潜在的分子机制。

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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.
机译:先天性肺病变包括广泛的罕见但临床上显着的发育异常,包括先天性囊性腺瘤样畸形,支气管肺隔离症,先天性大叶肺气肿和支气管源性囊肿,这些通常通过外科手术治疗。尽管先天性囊性腺瘤样畸形,支气管肺隔离症,先天性大叶肺气肿和支气管源性囊肿在临床上已根深蒂固,与刚性病理学定义相对应,但在发现中有相当多的重叠之处。忽略有关病变命名和分类的争议,先天性肺病变是由肺和气道胚胎发生的扰动引起的,这一点已被广泛接受。一般认为,胚胎学损伤的位置(气管支气管树的水平)和时间(胎龄)都与所显示的病变类型和组织病理学相关。这篇综述的目的是简要回顾一下正常的肺部发育并分析这些疾病的已知分子机制。

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