| Literature DB >> 22348466 |
S Rodrigo Burguete1, Stephanie M Levine, Marcos I Restrepo, Luis F Angel, Deborah J Levine, Jacqueline J Coalson, Jay I Peters.
Abstract
Williams-Campbell syndrome is a rare disorder characterized by deficiency of subsegmental bronchial cartilage and development of airway collapse and bronchiectasis that may subsequently progress to respiratory failure and death. There are only 2 published reports suggesting a familial association, and only one report of lung transplantation being used as a therapeutic modality. Due to postoperative airway complications, transplantation has not been recommended for this disease. We report the first lung transplant with prolonged survival, approaching 10 years, in a patient with Williams-Campbell syndrome, and provide further evidence to support a familial association. Copyright 2012 Daedalus EnterprisesEntities:
Mesh:
Year: 2012 PMID: 22348466 PMCID: PMC4066632 DOI: 10.4187/respcare.01484
Source DB: PubMed Journal: Respir Care ISSN: 0020-1324 Impact factor: 2.258