Congenital lung anomalies are a group of rare malformations, often diagnosed during the prenatal period. Guidelines on how to manage these patients are currently under debate, especially with regard to prophylactic surgery in asymptomatic patients, or how to proceed with conservative follow-up. Currently, there is no clear consensus on management strategies. A Swiss congenital lung anomaly national database and biobank was created in 2016 to enable data recording and collection of surgical lung samples in order to help define the most appropriate management strategies. This national observational cohort study represents an important step towards a better understanding of the pathophysiology and clinical course of the diseases included under congenital lung anomalies, especially in the context of a small country like Switzerland.

译文

先天性肺异常是一组罕见的畸形,通常在产前诊断。关于如何管理这些患者的指南目前正在争论中,特别是关于无症状患者的预防性手术,或如何进行保守随访。目前,在管理战略上还没有明确的共识。2016年创建了瑞士先天性肺异常国家数据库和生物库,以实现数据记录和手术肺样本收集,以帮助定义最合适的管理策略。这项国家观察性队列研究是朝着更好地了解先天性肺异常疾病的病理生理和临床过程迈出的重要一步,尤其是在像瑞士这样的小国的背景下。

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