Congenital cystic adenomatoid malformation type 0-a rare cause of neonatal death.
Pediatr Crit Care Med
; 8(6): 580-1, 2007 Nov.
Article
in En
| MEDLINE
| ID: mdl-17914309
ABSTRACT
OBJECTIVE:
We give the first account of failure of extracorporeal membrane oxygenation therapy secondary to congenital cystic malformation of the lung (CCAM) type 0.DESIGN:
Case report.SETTING:
Pediatric intensive care unit. PATIENT A female neonate, appropriate for gestational age, with respiratory failure immediately after delivery.INTERVENTIONS:
Cardiopulmonary support with venoarterial extracorporeal membrane oxygenation.RESULTS:
There was no improvement of pulmonary function, and the patient died. CCAM type 0 was diagnosed postmortem.CONCLUSIONS:
CCAM type 0 should be considered as a rare differential diagnosis of irreversible lung pathologies leading to failure of extracorporeal membrane oxygenation therapy for neonatal respiratory failure.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Respiratory Insufficiency
/
Cystic Adenomatoid Malformation of Lung, Congenital
Type of study:
Prognostic_studies
Limits:
Female
/
Humans
/
Newborn
Language:
En
Journal:
Pediatr Crit Care Med
Journal subject:
PEDIATRIA
/
TERAPIA INTENSIVA
Year:
2007
Document type:
Article
Affiliation country:
Germany