Abstract
Sarcoidosis involves the respiratory system in 90–95 % of patients, but has conventionally been viewed as a disease of lung parenchyma with restrictive physiologic abnormalities. However, granulomatous inflammation in sarcoidosis has a predilection for the airway submucosa, and therefore, clinical and subclinical airway involvement is common. Approximately 40–60 % of patients with sarcoidosis have some evidence of airway disease. Any structure from the tip of the nares to the terminal bronchioles may be affected. Since the symptoms from airway sarcoidosis are non-specific, diagnosis requires a high index of suspicion, supplemented by pulmonary function testing, imaging and direct fiberoptic visualization. Many of the airway manifestations of sarcoidosis are due to granulomatous inflammation and therefore treated with topical or systemic immunosuppressive medications. However, fibrotic sequelae of airway sarcoidosis generally require mechanical therapies such as bronchoplasty or debulking surgery, to relieve symptoms.
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Culver, D.A. (2016). Sarcoidosis of the Upper and Lower Airways. In: Mehta, A., Jain, P., Gildea, T. (eds) Diseases of the Central Airways. Respiratory Medicine. Humana Press, Cham. https://doi.org/10.1007/978-3-319-29830-6_2
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DOI: https://doi.org/10.1007/978-3-319-29830-6_2
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