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Williams–Campbell syndrome: a case report
INTRODUCTION: Williams–Campbell syndrome, also known as bronchomalacia, is a rare disorder characterized by a deficiency of cartilage in subsegmental bronchi, leading to distal airway collapse and bronchiectasis. There have been few reports about patients affected by saccular bronchiectasis, paracic...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265990/ https://www.ncbi.nlm.nih.gov/pubmed/22287845 http://dx.doi.org/10.2147/IJGM.S28447 |
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author | Konoglou, Maria Porpodis, Konstantinos Zarogoulidis, Paul Loridas, Nikolaos Katsikogiannis, Nikolaos Mitrakas, Alexandros Zervas, Vasilis Kontakiotis, Theodoros Papakosta, Despoina Boglou, Panagiotis Bakali, Stamatia Courcoutsakis, Nikolaos Zarogoulidis, Konstantinos |
author_facet | Konoglou, Maria Porpodis, Konstantinos Zarogoulidis, Paul Loridas, Nikolaos Katsikogiannis, Nikolaos Mitrakas, Alexandros Zervas, Vasilis Kontakiotis, Theodoros Papakosta, Despoina Boglou, Panagiotis Bakali, Stamatia Courcoutsakis, Nikolaos Zarogoulidis, Konstantinos |
author_sort | Konoglou, Maria |
collection | PubMed |
description | INTRODUCTION: Williams–Campbell syndrome, also known as bronchomalacia, is a rare disorder characterized by a deficiency of cartilage in subsegmental bronchi, leading to distal airway collapse and bronchiectasis. There have been few reports about patients affected by saccular bronchiectasis, paracicatricial emphysema, and diminished cartilage. These are all characteristic of Williams–Campbell syndrome. CASE PRESENTATION: This report presents a 57-year-old woman with progressive dyspnea, cough, sputum production, and fever. The clinical and laboratory examination revealed that the patient had a respiratory infection due to bronchiectasis caused by Williams–Campbell syndrome, which was undiagnosed in the patient until then. CONCLUSION: Although a rare syndrome, when patients’ signs and symptoms include recurrent respiratory infections, bronchiectasis, productive cough, and dyspnea, Williams–Campbell syndrome should be included in the differential diagnosis. |
format | Online Article Text |
id | pubmed-3265990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32659902012-01-27 Williams–Campbell syndrome: a case report Konoglou, Maria Porpodis, Konstantinos Zarogoulidis, Paul Loridas, Nikolaos Katsikogiannis, Nikolaos Mitrakas, Alexandros Zervas, Vasilis Kontakiotis, Theodoros Papakosta, Despoina Boglou, Panagiotis Bakali, Stamatia Courcoutsakis, Nikolaos Zarogoulidis, Konstantinos Int J Gen Med Case Report INTRODUCTION: Williams–Campbell syndrome, also known as bronchomalacia, is a rare disorder characterized by a deficiency of cartilage in subsegmental bronchi, leading to distal airway collapse and bronchiectasis. There have been few reports about patients affected by saccular bronchiectasis, paracicatricial emphysema, and diminished cartilage. These are all characteristic of Williams–Campbell syndrome. CASE PRESENTATION: This report presents a 57-year-old woman with progressive dyspnea, cough, sputum production, and fever. The clinical and laboratory examination revealed that the patient had a respiratory infection due to bronchiectasis caused by Williams–Campbell syndrome, which was undiagnosed in the patient until then. CONCLUSION: Although a rare syndrome, when patients’ signs and symptoms include recurrent respiratory infections, bronchiectasis, productive cough, and dyspnea, Williams–Campbell syndrome should be included in the differential diagnosis. Dove Medical Press 2012-01-11 /pmc/articles/PMC3265990/ /pubmed/22287845 http://dx.doi.org/10.2147/IJGM.S28447 Text en © 2012 Konoglou et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Case Report Konoglou, Maria Porpodis, Konstantinos Zarogoulidis, Paul Loridas, Nikolaos Katsikogiannis, Nikolaos Mitrakas, Alexandros Zervas, Vasilis Kontakiotis, Theodoros Papakosta, Despoina Boglou, Panagiotis Bakali, Stamatia Courcoutsakis, Nikolaos Zarogoulidis, Konstantinos Williams–Campbell syndrome: a case report |
title | Williams–Campbell syndrome: a case report |
title_full | Williams–Campbell syndrome: a case report |
title_fullStr | Williams–Campbell syndrome: a case report |
title_full_unstemmed | Williams–Campbell syndrome: a case report |
title_short | Williams–Campbell syndrome: a case report |
title_sort | williams–campbell syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265990/ https://www.ncbi.nlm.nih.gov/pubmed/22287845 http://dx.doi.org/10.2147/IJGM.S28447 |
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