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Pediatric Allergy and Respiratory Disease ; : 434-439, 2009.
Article in Korean | WPRIM | ID: wpr-22308

ABSTRACT

Congenital cystic disease of the lung represents pulmonary sequestration, congenital lobar emphysema, bronchogenic cyst and congenital cystic adenomatoid malformation. It has a variety of clinical manifestations from immediate postnatal respiratory distress to heart failure. Pulmonary sequestration sometimes causes heart failure in neonates through a shunt between an anomalous systemic feeding artery and the pulmonary venous system. We hereby report a case with both pulmonary sequestration and congenital lobar emphysema presenting with congestive heart failure and pulmonary hypertension, which improved after lobectomy.


Subject(s)
Humans , Infant, Newborn , Arteries , Bronchogenic Cyst , Bronchopulmonary Sequestration , Cystic Adenomatoid Malformation of Lung, Congenital , Emphysema , Estrogens, Conjugated (USP) , Heart Failure , Hypertension, Pulmonary , Lung , Pulmonary Emphysema
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