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2
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本文引用的文献

1
Impact of perinatal hypoxia on the developing brain.围产期缺氧对发育中大脑的影响。
Physiol Res. 2020 Apr 30;69(2):199-213. doi: 10.33549/physiolres.934198. Epub 2020 Mar 23.
2
Congenital Lung Malformations: Unresolved Issues and Unanswered Questions.先天性肺发育异常:未解决的问题与未解答的疑问
Front Pediatr. 2019 Jun 13;7:239. doi: 10.3389/fped.2019.00239. eCollection 2019.
3
The Use of Fetal Bronchoscopy in the Diagnosis and Management of a Suspected Obstructive Lung Mass.胎儿支气管镜检查在疑似阻塞性肺肿块诊断和管理中的应用
AJP Rep. 2018 Jul;8(3):e195-e200. doi: 10.1055/s-0038-1673378. Epub 2018 Sep 25.
4
Novel Molecular and Phenotypic Insights into Congenital Lung Malformations.先天性肺畸形的新分子和表型见解。
Am J Respir Crit Care Med. 2018 May 15;197(10):1328-1339. doi: 10.1164/rccm.201706-1243OC.
5
Congenital high airway obstruction syndrome (CHAOS): discussing the role and limits of prenatal diagnosis starting from a single-center case series.先天性高气道梗阻综合征(CHAOS):从单中心病例系列探讨产前诊断的作用及局限性
J Prenat Med. 2016 Jan-Jun;10(1-2):4-7. doi: 10.11138/jpm/2016.10.1.004.
6
Current Management of Congenital Pulmonary Airway Malformations: A "European Pediatric Surgeons' Association" Survey.先天性肺气道畸形的当前管理:“欧洲小儿外科医生协会”调查
Eur J Pediatr Surg. 2018 Feb;28(1):1-5. doi: 10.1055/s-0037-1604020. Epub 2017 Jul 14.
7
Prenatal interventions for fetal lung lesions.胎儿肺部病变的产前干预措施。
Prenat Diagn. 2011 Jul;31(7):628-36. doi: 10.1002/pd.2778. Epub 2011 May 25.
8
Congenital lung malformations.先天性肺畸形。
J Bras Pneumol. 2011 Mar-Apr;37(2):259-71. doi: 10.1590/s1806-37132011000200017.
9
Surgical treatment of 60 patients with pulmonary malformations: what have we learned?60例肺畸形患者的外科治疗:我们学到了什么?
J Bras Pneumol. 2008 Sep;34(9):661-6. doi: 10.1590/s1806-37132008000900005.
10
Prenatal diagnosis and outcome of echogenic fetal lung lesions.胎儿肺强回声病变的产前诊断及结局
Ultrasound Obstet Gynecol. 2008 Nov;32(6):769-83. doi: 10.1002/uog.6218.

新生儿呼吸功能不全的罕见病因。

Rare causes of respiratory insufficiency in newborns.

机构信息

Neonatal Department of Intensive Medicine Comenius University in Bratislava, National Institute of Children's Diseases, Bratislava, Slovak Republic.

出版信息

Physiol Res. 2020 Dec 31;69(Suppl 4):S637-S647. doi: 10.33549/physiolres.934613.

DOI:10.33549/physiolres.934613
PMID:33646006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8603702/
Abstract

Congenital lung masses (CLM) the rare group of causes of acute respiratory insufficiency (RI) in newborns include congenital airway pulmonary malformation (CAPM), congenital overinflation, bronchopulmonary sequestration, and bronchial atresia. The presenting group consists of 13 newborns who were admitted to the Neonatal Department of Intensive Medicine (NDIM) during January 1st 2015-December 31st 2019 (8 males, 5 females, 2 premature/11 term newborns, spontaneous delivery: 2, caesarean section: 11) with positive prenatal diagnosis of CAPM in all cases. In 2 cases prenatal intervention was performed (drainage of the amniotic fluid, attempt of thoracentesis). Signs of acute RI immediately after delivery were seen in 5 newborns. Postnatal echocardiographic investigation confirmed the presence of increased pulmonary pressure in 8 patients, no patient had congenital heart abnormality. A thorax x-ray was positive also in asymptomatic patients. Computed tomography in patients brought detailed information about the position, size and character of CAPM. Six patients underwent surgery. In 15.4 % right lungs were affected by cystic malformation and in 23 % left lungs were affected. A final diagnosis of CAPM was confirmed in 5 patients using histopathologic examination. Multidisciplinary cooperation during prenatal as well as postnatal period is necessary.

摘要

先天性肺肿块(CLM)是导致新生儿急性呼吸功能不全(RI)的罕见病因群,包括先天性气道肺畸形(CAPM)、先天性过度充气、肺隔离症和支气管闭锁。本研究组包括 13 名于 2015 年 1 月 1 日至 2019 年 12 月 31 日期间入住新生儿重症监护病房(NDIM)的新生儿(8 名男性,5 名女性,2 名早产儿/11 名足月儿,自然分娩:2 例,剖宫产:11 例),所有病例均有 CAPM 的产前阳性诊断。2 例进行了产前干预(羊水引流、胸腔穿刺尝试)。5 例新生儿在出生后立即出现急性 RI 征象。8 例患者的产后超声心动图检查证实存在肺动脉高压,无患者存在先天性心脏病异常。无症状患者的胸部 X 线也呈阳性。CT 检查为患者提供了关于 CAPM 的位置、大小和特征的详细信息。6 名患者接受了手术。囊性畸形累及右肺的比例为 15.4%,左肺的比例为 23%。5 名患者通过组织病理学检查最终确诊为 CAPM。产前和产后的多学科合作是必要的。