Congenital pulmonary airway malformation
Autops. Case Rep
;
8(2): e2018022, Apr.-May 2018. ilus
Article
Dans Anglais
| LILACS
| ID: biblio-905523
ABSTRACT
Congenital pulmonary airway malformation (CPAM) is a developmental malformation of the lower respiratory tract. We report the case of a male newborn diagnosed with cystic lung disease during prenatal ultrasound. A cesarean section was performed at the 32nd gestational week because of premature rupture of the membranes, and soon after the delivery the newborn developed respiratory failure and died. The aim of this study is to report an autopsy case because of its rarity, and to briefly discuss the CPAM subtypes and differential diagnosis of cystic lung diseases of childhood.
Texte intégral:
Disponible
Indice:
LILAS (Amériques)
Sujet Principal:
Diagnostic prénatal
/
Malformation congénitale kystique adénomatoïde du poumon
Type d'étude:
Etude diagnostique
/
Etude d'étiologie
Limites du sujet:
Femelle
/
Humains
/
Nouveau-né
/
Grossesse
langue:
Anglais
Texte intégral:
Autops. Case Rep
Thème du journal:
Anatomia
/
Patologia Cl¡nica
/
Patologia Legal
Année:
2018
Type:
Article
Pays d'affiliation:
Brésil
Institution/Pays d'affiliation:
Hospital Guilherme Alvaro Santos/BR
/
Metropolitan University of Santos/BR
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