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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
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.
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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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