Literature DB >> 22348466

Lung transplantation for Williams-Campbell syndrome with a probable familial association.

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 Enterprises

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Year:  2012        PMID: 22348466      PMCID: PMC4066632          DOI: 10.4187/respcare.01484

Source DB:  PubMed          Journal:  Respir Care        ISSN: 0020-1324            Impact factor:   2.258


  18 in total

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  3 in total

Review 1.  Tracheal and bronchial stenoses and other obstructive conditions.

Authors:  Claudia Schweiger; Aliza P Cohen; Michael J Rutter
Journal:  J Thorac Dis       Date:  2016-11       Impact factor: 2.895

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Authors:  Alexandre Dias Mançano; Rubens Carneiro Dos Santos Neto; Karla Coelho Caixeta E Silva
Journal:  Radiol Bras       Date:  2014 Mar-Apr

Review 3.  The clinical manifestations, diagnosis and management of williams-campbell syndrome.

Authors:  Adrian Pedro Noriega Aldave; DO William Saliski
Journal:  N Am J Med Sci       Date:  2014-09
  3 in total

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