Congenital cystic adenomatoid malformation type I

Congenital cystic adenomatoid malformation (CCAM) is an hamartomatous congenital pulmonary airway malformation with incidence ranging between 1:10,000 and 1:35,000 newborns. Currently CCAM is classified into five groups according to clinical and pathological features. The clinical outcome varies dep...

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Bibliographic Details
Main Authors: Alice Rebelo de Matos Borges dos Reis (Author), Frederico Becker Ribeiro (Author), Regina Schultz (Author)
Format: Book
Published: University of São Paulo, 2015-09-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Alice Rebelo de Matos Borges dos Reis  |e author 
700 1 0 |a Frederico Becker Ribeiro  |e author 
700 1 0 |a Regina Schultz  |e author 
245 0 0 |a Congenital cystic adenomatoid malformation type I 
260 |b University of São Paulo,   |c 2015-09-01T00:00:00Z. 
500 |a 2236-1960 
520 |a Congenital cystic adenomatoid malformation (CCAM) is an hamartomatous congenital pulmonary airway malformation with incidence ranging between 1:10,000 and 1:35,000 newborns. Currently CCAM is classified into five groups according to clinical and pathological features. The clinical outcome varies depending on the subtype and the extent of involvement. The authors report the case of a premature male newborn with the prenatal diagnosis of CCAM Type 1 associated with cardiac right axis deviation, who died 67 hours after birth due to respiratory failure. In addition to the autopsy report of this rare entity, the authors present its classification and prognosis. 
546 |a EN 
690 |a Cystic Adenomatoid Malformation of Lung 
690 |a Congenital 
690 |a Classification 
690 |a Prognosis 
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 3 (2015) 
787 0 |n http://www.revistas.usp.br/autopsy/article/view/107015 
787 0 |n https://doaj.org/toc/2236-1960 
856 4 1 |u https://doaj.org/article/6e8b22c62a2b4b9188567b5c18949b01  |z Connect to this object online.