Your browser doesn't support javascript.
loading
Constrictive Bronchiolitis in Cystic Fibrosis Adolescents with Refractory Pulmonary Decline.
Harris, William T; Boyd, J Todd; McPhail, Gary L; Brody, Alan S; Szczesniak, Rhonda D; Korbee, Leslie L; Baker, Michael L; Clancy, John P.
Afiliação
  • Harris WT; 1 Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.
  • Boyd JT; 2 Department of Pathology, Dayton Children's Hospital, Dayton, Ohio.
  • McPhail GL; 3 Division of Pulmonary Medicine.
  • Brody AS; 4 Department of Radiology.
  • Szczesniak RD; 3 Division of Pulmonary Medicine.
  • Korbee LL; 5 Division of Biostatistics and Epidemiology, and.
  • Baker ML; 6 Office for Clinical and Translational Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; and.
  • Clancy JP; 7 Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio.
Ann Am Thorac Soc ; 13(12): 2174-2183, 2016 12.
Article em En | MEDLINE | ID: mdl-27684511
ABSTRACT
RATIONALE Refractory lung function decline in association with recurrent pulmonary exacerbations is a common, yet poorly explained finding in cystic fibrosis (CF). To investigate the histopathologic mechanisms of pulmonary deterioration during adolescence and early adulthood, we reviewed clinically-indicated lung biopsy specimens obtained during a period of persistent decline.

OBJECTIVES:

To determine if peribronchiolar remodeling is prominent in lung biopsy specimens obtained in adolescents with CF refractory to conventional therapy.

METHODS:

Six adolescents with CF (mean age, 16.2 y; mean FEV1, 52% predicted at biopsy) with significant pulmonary deterioration over 12-24 months (mean FEV1 decline of 14% predicted/year) despite aggressive intervention underwent computed tomography imaging and ultimately lung biopsy to aid clinical management. In addition to routine clinical evaluation, histopathologic investigation included staining for transforming growth factor-ß (TGF-ß, a genetic modifier of CF lung disease), collagen deposition (a marker of fibrosis), elastin (to evaluate for bronchiectasis), and α-smooth muscle actin (to identify myofibroblasts). MEASUREMENTS AND MAIN

RESULTS:

All computed tomography scans demonstrated a mix of bronchiectasis and hyperinflation that was variable across lung regions and within patients. Lung biopsy revealed significant peribronchiolar remodeling, particularly in patients with more advanced disease, with near complete obliteration of the peribronchiolar lumen (constrictive bronchiolitis). Myofibroblast differentiation (a TGF-ß-dependent process) was prominent in specimens with significant airway remodeling.

CONCLUSIONS:

Constrictive bronchiolitis is widely present in the lung tissue of adolescents with CF with advanced disease and may contribute to impaired lung function that is refractory to conventional therapy (antibiotics, antiinflammatories, and mucolytics). TGF-ß-dependent myofibroblast differentiation is prominent in areas of active fibrogenesis and may foster small airway remodeling in CF lung disease.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Bronquiolite Obliterante / Fibrose Cística / Remodelação das Vias Aéreas / Pulmão Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Ann Am Thorac Soc Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Bronquiolite Obliterante / Fibrose Cística / Remodelação das Vias Aéreas / Pulmão Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Ann Am Thorac Soc Ano de publicação: 2016 Tipo de documento: Article