Pulmonary agenesis and respiratory failure in childhood

Pulmonary agenesis (PA) is a rare congenital anomaly, which may be unilateral or bilateral. Unilateral PA may be associated with nonspecific respiratory symptoms. We report the case of 5-month-old infant who presented a normal development until the age of 4 months when a respiratory infection caused...

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Những tác giả chính: Paula Vanessa Valverde Dinamarco (Tác giả), Cesar Cilento Ponce (Tác giả)
Định dạng: Sách
Được phát hành: University of São Paulo, 2015-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Paula Vanessa Valverde Dinamarco  |e author 
700 1 0 |a Cesar Cilento Ponce  |e author 
245 0 0 |a Pulmonary agenesis and respiratory failure in childhood 
260 |b University of São Paulo,   |c 2015-03-01T00:00:00Z. 
500 |a 10.4322/acr.%y.98453 
500 |a 2236-1960 
520 |a Pulmonary agenesis (PA) is a rare congenital anomaly, which may be unilateral or bilateral. Unilateral PA may be associated with nonspecific respiratory symptoms. We report the case of 5-month-old infant who presented a normal development until the age of 4 months when a respiratory infection caused an acute respiratory distress syndrome with a fatal outcome. The autopsy findings depicted the right lung agenesis without any other concomitant malformation. Although respiratory symptoms represent frequent complaints in pediatrics, the aim of this study is not only to draw attention to the unilateral pulmonary agenesis as a possible underlying malformation in children who present recurrent and severe respiratory symptoms, but also to report a case diagnosed at autopsy. 
546 |a EN 
690 |a Lung agenesis 
690 |a Respiratory Insufficiency 
690 |a Autopsy 
690 |a Medicine 
690 |a R 
690 |a Internal medicine 
690 |a RC31-1245 
655 7 |a article  |2 local 
786 0 |n Autopsy and Case Reports, Vol 5, Iss 1 (2015) 
787 0 |n http://www.revistas.usp.br/autopsy/article/view/98453 
787 0 |n https://doaj.org/toc/2236-1960 
856 4 1 |u https://doaj.org/article/d3408d7f735c44e28aa1b24554cae5b2  |z Connect to this object online.