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法洛四联症合并肺动脉瓣缺如综合征中的2型先天性肺气道畸形

Type 2 Congenital Pulmonary Airway Malformation in Tetralogy of Fallot with Absent Pulmonary Valve Syndrome.

作者信息

Singh Damandeep, Ojha Vineeta, Mukherjee Aprateem, Kadiyani Lamak, Kumar Sanjeev

机构信息

Department of Cardiovascular Radiology and Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.

Department of Cardiology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Indian J Radiol Imaging. 2025 Mar 27;35(4):596-598. doi: 10.1055/s-0045-1802669. eCollection 2025 Oct.

Abstract

Tetralogy of Fallot with absent pulmonary valve syndrome is a unique congenital condition often accompanied with dilated pulmonary arteries causing varied degree of airway compression. Frequently, abnormal pulmonary arterial branching at the segmental level and compression at the level of intrapulmonary bronchi can be seen. The occurrence of isolated bronchopulmonary malinosculation in the form of congenital pulmonary airway malformation is exceedingly rare. This report highlights a case of such rarity, involving a young child with recurrent lower respiratory tract infections.

摘要

法洛四联症合并肺动脉瓣缺如综合征是一种独特的先天性疾病,常伴有肺动脉扩张,导致不同程度的气道受压。通常可见节段水平的肺动脉分支异常和肺内支气管水平的受压情况。以先天性肺气道畸形形式出现的孤立性支气管肺错构瘤极为罕见。本报告重点介绍了这样一例罕见病例,涉及一名反复发生下呼吸道感染的幼儿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56fb/12440583/3fc3867161eb/10-1055-s-0045-1802669-i2494070-1.jpg

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