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先天性高位气道梗阻序列征胎儿的产前磁共振成像表现

Prenatal MRI findings of fetuses with congenital high airway obstruction sequence.

作者信息

Guimaraes Carolina V A, Linam Leann E, Kline-Fath Beth M, Donnelly Lane F, Calvo-Garcia Maria A, Rubio Eva I, Livingston Jeffrey C, Hopkin Robert J, Peach Elizabeth, Lim Foong-Yen, Crombleholme Timothy M

机构信息

Department of Radiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229-3039, USA.

出版信息

Korean J Radiol. 2009 Mar-Apr;10(2):129-34. doi: 10.3348/kjr.2009.10.2.129. Epub 2009 Mar 3.

Abstract

OBJECTIVE

To define the MRI findings of congenital high airway obstruction sequence (CHAOS) in a series of fetuses.

MATERIALS AND METHODS

Prenatal fetal MR images were reviewed in seven fetuses with CHAOS at 21 to 27 weeks of gestation. The MRI findings were reviewed. The MRI parameters evaluated included the appearance of the lungs and diaphragm, presence or absence of hydrops, amount of amniotic fluid, airway appearance, predicted level of airway obstruction, and any additional findings or suspected genetic syndromes.

RESULTS

All the fetuses viewed (7 of 7) demonstrated the following MRI findings: dilated airway below the level of obstruction, increased lung signal, markedly increased lung volumes with flattened or inverted hemidiaphragms, massive ascites, centrally positioned and compressed heart, as well as placentomegaly. Other frequent findings were anasarca (6 of 7) and polyhydramnios (3 of 7). MRI identified the level of obstruction as laryngeal in five cases and tracheal in two cases. In four of the patients, surgery or autopsy confirmed the MRI predicted level of obstruction. Associated abnormalities were found in 4 of 7 (genetic syndromes in 2). Postnatal radiography (n = 3) showed markedly hyperinflated lungs with inverted or flattened hemidiaphragms, strandy perihilar opacities, pneumothoraces and tracheotomy. Two fetuses were terminated and one fetus demised in utero. Four fetuses were delivered via ex utero intrapartum treatment procedure.

CONCLUSION

MRI shows a consistent pattern of abnormalities in fetuses with CHAOS, accurately identifies the level of airway obstruction, and helps differentiate from other lung abnormalities such as bilateral congenital pulmonary airway malformation by demonstrating an abnormally dilated airway distal to the obstruction.

摘要

目的

明确一系列胎儿先天性高气道梗阻序列征(CHAOS)的MRI表现。

材料与方法

回顾了7例妊娠21至27周患有CHAOS的胎儿的产前MRI图像。对MRI表现进行了评估。评估的MRI参数包括肺和膈肌的表现、有无水肿、羊水量、气道表现、气道梗阻的预测水平以及任何其他发现或疑似遗传综合征。

结果

所有观察的胎儿(7/7)均表现出以下MRI表现:梗阻水平以下气道扩张、肺信号增强、肺容积明显增加伴半膈肌变平或倒置、大量腹水、心脏居中并受压以及胎盘肿大。其他常见表现为全身性水肿(6/7)和羊水过多(3/7)。MRI确定5例梗阻位于喉部,2例位于气管。4例患者的手术或尸检证实了MRI预测的梗阻水平。7例中有4例发现相关异常(2例为遗传综合征)。产后X线检查(n = 3)显示肺明显过度充气伴半膈肌倒置或变平、肺门周围条索状模糊影、气胸和气管切开。2例胎儿终止妊娠,1例胎儿宫内死亡。4例胎儿通过产时宫外治疗程序分娩。

结论

MRI显示CHAOS胎儿存在一致的异常模式,能准确识别气道梗阻水平,并通过显示梗阻远端气道异常扩张,有助于与其他肺部异常如双侧先天性肺气道畸形相鉴别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9864/2651442/7c7bbe3b48b3/kjr-10-129-g001.jpg

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