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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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Detalles Bibliográficos
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
Descripción
Sumario: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.