Literature DB >> 18377543

Right aortic coarctation and ventricular septal defect: an unusual cause of tracheal compression in infancy.

Manuel Caceres1, Casey Daggett, Joel Lutterman, Christian Gilbert.   

Abstract

OBJECTIVE: Acyanotic congenital heart diseases may occasionally present with tracheobronchial obstruction. Increased pulmonary blood flow against a high-resistance pulmonary bed may create significant pulmonary artery dilation.
METHODS: We report an unusual case of ventricular septal defect and right aortic arch coarctation, complicated with distal tracheal compression secondary to a pincer effect created by a right aortic arch and a massively dilated pulmonary artery.
RESULTS: High index of suspicion is required to anticipate tracheobronchial compression in acyanotic congenital heart diseases.
CONCLUSION: Fiberoptic bronchoscopy is an invaluable tool to assess for tracheal compression relief following surgical repair and to identify tracheomalacia prior to extubation.

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Year:  2006        PMID: 18377543     DOI: 10.1111/j.1747-0803.2006.00030.x

Source DB:  PubMed          Journal:  Congenit Heart Dis        ISSN: 1747-079X            Impact factor:   2.007


  1 in total

1.  Right aortic arch with coarctation in Chinese children.

Authors:  Zhu Ming; Sun Aimin
Journal:  Pediatr Radiol       Date:  2008-02-02
  1 in total

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