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References in periodicals archive ?
Cass, "Congenital lobar emphysema: like father, like son," Journal of Pediatric Surgery, vol.
Caption: FIGURE 1: Chest radiographs of neonate showing features of hyaline membrane disease on day 1 of life and typical features of left upper lobe congenital lobar emphysema (CLE) on day 25 of life.
Cataneo, "Congenital lobar emphysema: 30-year case series in two university hospitals," Jornal Brasileiro de Pneumologia, vol.
Ince, "Congenital lobar emphysema: a rare cause of hypertension," Saudi Medical Journal, vol.
Congenital lobar emphysema is characterized by over inflation of the pulmonary lobe (gas trapping) and is caused by localized bronchial obstruction.9,10The causative factor can be found only in half of the cases which include either partial bronchial obstruction or intrinsic alveolar disease.
Congenital lobar emphysema most often detected in the neonates or antenatally; however, less severely affected patients may present either in infancy or early childhood.16,17 The manifestation of CLE is usually a progressive severe form of respiratory distress.
Congenital Lobar emphysema (CLE) is a rare anomaly with an incidence of 1:20,000 to 1:30,000 live births.1 It is due to over inflation of a lobe resulting from intrinsic deficiency of bronchial cartilage and elastic tissue with most common involvement is of the left upper lobe followed by right upper lobe and right middle lobe.2
The histopathological parameters chosen for the diagnosis of congenital lobar emphysema were found to be very useful, adjunct to the routine description.
Congenital lobar emphysema: Differential diagnosis and therapeutic approach.
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