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先天性肺气道畸形：成人期的罕见诊断。

Congenital pulmonary airway malformation: A rare diagnosis in adulthood.

作者信息

Viana Raquel, Carvalho Lina, Santos Cláudia

机构信息

Pulmonology Department Centro Hospitalar de Leiria Leiria Portugal.

Anatomical Pathology Unit Centro Hospitalar Universitário de Coimbra Coimbra Portugal.

出版信息

Respirol Case Rep. 2021 Dec 20;10(1):e0895. doi: 10.1002/rcr2.895. eCollection 2022 Jan.

DOI:10.1002/rcr2.895
PMID:34976401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8688662/
Abstract

This paper consists of a clinical image of a complex developmental anomaly that is usually diagnosed prenatally or during childhood. Its detection in adult life is very rare, as happened in the present case.

摘要

本文包含一张复杂发育异常的临床图像，这种异常通常在产前或儿童期被诊断出来。像本病例这样在成年期才被发现的情况非常罕见。

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引用本文的文献

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Congenital pulmonary airway malformation presenting as a solid mass: a description of two cases and a literature analysis.表现为实性肿块的先天性肺气道畸形：两例病例描述及文献分析
Quant Imaging Med Surg. 2024 Dec 5;14(12):9805-9812. doi: 10.21037/qims-24-1208. Epub 2024 Nov 14.
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Congenital Cystic Adenomatoid Malformation (CCAM) Type II: A Rare Case of Sudden Infant Death.先天性囊性腺瘤样畸形（CCAM）II型：一例罕见的婴儿猝死病例。
Children (Basel). 2022 Nov 26;9(12):1830. doi: 10.3390/children9121830.

本文引用的文献

1
Cystic adenomatoid pulmonary malformation in adults: A retrospective study in a tertiary university hospital.
Rev Port Pneumol (2006). 2017 Mar-Apr;23(2):109-110. doi: 10.1016/j.rppnen.2016.10.005. Epub 2017 Jan 7.
2
Case report: Congenital cystic adenomatoid malformation of an entire lung in a 33-year-old man: a case report and review of the literature.病例报告：一名33岁男性全肺先天性囊性腺瘤样畸形：病例报告及文献复习
Br J Radiol. 2008 Nov;81(971):e276-8. doi: 10.1259/bjr/23523404.