| Literature DB >> 21841334 |
Hiroshi Wada1, Ruriko Seto, Hideto Yamada, Taishi Nagao, Takashi Hajiro, Yasutaka Nakano.
Abstract
Williams-Campbell syndrome is a rare disease, characterized by a congenital deficiency of cartilage in the fourth to sixth order bronchi, leading to chronic respiratory failure with recurrent pulmonary infections. An effective and practical treatment has not yet been established. A 31-year-old man who was diagnosed as Williams-Campbell syndrome by inspiratory and expiratory computed tomography findings developed recurrent pulmonary infections and showed progressive deterioration of dyspnea. Domiciliary NPPV was administered, followed by a dramatic improvement of respiratory failure and a decrease in the episodes of pulmonary infections. NPPV may have an advantage in adults with Williams-Campbell syndrome who have severe respiratory failure and recurrent pulmonary infections.Entities:
Mesh:
Year: 2011 PMID: 21841334 DOI: 10.2169/internalmedicine.50.4971
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271