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肺动脉高压与先天性支气管闭锁:一种时间因素关联。

Pulmonary hypertension and congenital bronchial atresia: A time factor association.

作者信息

Alebna Prince A, Kim David H, Chaudhary Raghav, Tavares Matthew

机构信息

Englewood Health, Englewood, NJ, United States.

George Washington University, Washington, DC, United States.

出版信息

Respir Med Case Rep. 2019 Jun 15;28:100882. doi: 10.1016/j.rmcr.2019.100882. eCollection 2019.

Abstract

Congenital bronchial atresia is rarely symptomatic in adults. Recurrent lung infection and pneumothorax are the feared complications of this otherwise benign condition. The objective of this article is to present a case of congenital bronchial atresia manifesting as pulmonary hypertension in a 66 year-old patient. While doing so, we highlight the relevant knowledge accrued in medical literature with regards this rare condition. Finally, with the revelation that congenital bronchial atresia may cause severe pulmonary hypertension later in life, perhaps a less conservative approach to management may be warranted in younger adults and children with this condition.

摘要

先天性支气管闭锁在成人中很少有症状。反复肺部感染和气胸是这种原本良性疾病令人担忧的并发症。本文的目的是介绍一例66岁患者表现为肺动脉高压的先天性支气管闭锁病例。在此过程中,我们强调了医学文献中关于这种罕见疾病积累的相关知识。最后,鉴于先天性支气管闭锁可能在生命后期导致严重的肺动脉高压,对于患有这种疾病的年轻人和儿童,或许有必要采取不那么保守的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/6597737/de57bea56460/gr1.jpg

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