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[双侧肺发育不全罕见病例及产前诊断]

[Rare case of bilateral pulmonary agenesis and prenatal diagnosis].

作者信息

Veluppillai C, Jossic F, Quéré M-P, Philippe H-J, Le Vaillant C

机构信息

Service de gynécologie obstétrique, CHU de Nantes, quai 38, boulevard Jean-Monnet, 44093 Nantes cedex, France.

Service de fœtopathologie, CHU de Nantes, quai 38, boulevard Jean-Monnet, 44093 Nantes cedex, France.

出版信息

Gynecol Obstet Fertil. 2014 Jul-Aug;42(7-8):533-6. doi: 10.1016/j.gyobfe.2014.05.007. Epub 2014 Jun 13.

Abstract

Bilateral pulmonary agenesis (BPA) is a rare congenital lung malformation. The prognosis is severe as it is incompatible with extra-uterine life. Although multiple prenatal imaging modalities are developed, the prenatal diagnosis of BPA remains problematic. We report a case of BPA observed in our unity and for which the diagnosis was not clearly identified during the evaluation. This report illustrates the need to consider all the imaging aspects and particularly during US examination suspecting BPA.

摘要

双侧肺不发育(BPA)是一种罕见的先天性肺畸形。其预后严重,因为它与宫外生活不相容。尽管已经开发了多种产前成像方式,但BPA的产前诊断仍然存在问题。我们报告了一例在我们科室观察到的BPA病例,在评估过程中诊断并不明确。本报告说明了需要考虑所有成像方面,尤其是在超声检查怀疑BPA时。

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