医学
气胸
支气管扩张
怀孕
剖腹产
儿科
哮喘
外科
内科学
肺
遗传学
生物
作者
A. Avital,Ori Galante,Joel Baron,Alexander Smoliakov,Dov Heimer,Lone Avnun
出处
期刊:Case Reports
[BMJ]
日期:2009-11-18
卷期号:2009 (nov18 1): bcr0720092068-bcr0720092068
被引量:4
标识
DOI:10.1136/bcr.07.2009.2068
摘要
The present report concerns a young woman previously diagnosed as having childhood asthma who presented with a secondary spontaneous pneumothorax during the third trimester of pregnancy; at term a caesarean section was recommended for safety reasons. Post partum a severe fixed ventilatory defect unresponsive to inhaled bronchodilator and a short oral course of steroids ruled out asthma. Diffuse bronchiectasis was found on her chest CT scan, although this was not evident clinically. Known aetiologies for diffuse bronchiectasis (cystic fibrosis, anti-α1 antitrypsin deficiency, rheumatic diseases, mycobacterial infections, childhood infections and immune deficiencies) were ruled out. Therefore it is believed her bronchiectasis was idiopathic or congenital. No recommendations from recent guidelines on how to manage labour in a woman after a spontaneous pneumothorax could be found. However, a literature search revealed that pregnant women usually experience primary pneumothorax and may continue in natural labour; however, it is unknown how best to manage a woman with secondary spontaneous pneumothorax.
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