Prenatal and Postnatal Management of Congenital Pulmonary Airway Malformation

被引:80
|
作者
David, Mafalda [1 ]
Lamas-Pinheiro, Ruben [1 ]
Henriques-Coelho, Tiago [1 ,2 ]
机构
[1] Ctr Hosp Sao Joao, Dept Pediat Surg, Oporto, Portugal
[2] Univ Porto, Fac Med, Dept Pediat, P-4200319 Oporto, Portugal
关键词
Congenital malformations; Lung development; Macrocystic pulmonary lesion; Microcystic pulmonary lesion; Thoracoscopic lobectomy; Lung cancer risk; CYSTIC ADENOMATOID MALFORMATION; FETAL LUNG LESIONS; MUCINOUS BRONCHIOLOALVEOLAR CARCINOMA; I PLEUROPULMONARY BLASTOMA; ENDOTHELIAL GROWTH-FACTOR; OF-THE-LITERATURE; BRONCHOPULMONARY SEQUESTRATION; THORACIC MALFORMATIONS; MATERNAL BETAMETHASONE; MOLECULAR-MECHANISMS;
D O I
10.1159/000440894
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Congenital pulmonary airway malformation (CPAM) is one of the most common lung lesions detected prenatally. Despite the research efforts made in the past few years, controversy and lack of clarity in the literature still exist regarding nomenclature, classification, pathogenesis and the management of CPAM. Therefore, it is of greatest importance to delineate the natural history of CPAMs and to create a consensus to guide the management and follow-up of these lesions. This review will focus on classification systems, highlighting the most recent advancements in pathogenesis, and current practice in the prenatal diagnosis of CPAM. Strategies of prenatal management and postnatal management will be reviewed. Long-term follow-up, including lung cancer risk, is discussed and an outcome perspective is presented. (C) 2016 S. Karger AG, Basel.
引用
收藏
页码:101 / 115
页数:15
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