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Tokyo University Hospital Tokyo, Japan
To the Editor:
In a recent issue of CHEST (November 1998), Judson and Strange1 rationally discussed that sarcoidosis caused bullous emphysema through the three cases of pulmonary sarcoidosis.
Although bullae may occur in subjects with otherwise healthy lungs, most bullae develop in smokers with centrilobular emphysema. Thus, cigarette smoking is considered to be an utmost risk factor in the development of bullous emphysema. However, the mechanism and cause of bullous emphysema have not fully been elucidated. Therefore, the current comprehensive report is important.
Giant bullae can occur in patients with sarcoidosis and advanced stages
of the disease, and appear to be bullous emphysema or vanishing lung
syndrome.2
,3
,4
,5
Although emphysema increases in frequency
with age and is found most frequently in patients in the seventh
decade, bullous emphysema is predominantly found in young patients.
Further, the surgical procedures, including lung volume reduction
surgery, are particularly beneficial for those who have bullous
emphysema as well as bullous sarcoidosis.5
,6
,7
,8
Sarcoidosis
should be carefully considered in the differential diagnosis of bullous
emphysema in young patients with chronic airflow limitation (CAL), in
addition to the other hereditary disorders, including
1-antitrypsin deficiency, Fabry's disease, Salla
disease, cutis laxa, and Ehlers-Danlos syndrome.5
There is
no doubt that sarcoidosis is a cause of bullous emphysema in young
patients with CAL; however, the pathogenesis of large bullae in
patients with sarcoidosis remains to be determined.
Interestingly, bullous emphysema can be found in dogs, cats, and pups. Hoover and colleagues9 suggested that congenital weakness of the bronchial cartilage and lung torsion might be involved in the development of bullous emphysema in the pup. This may, in part, support the authors' hypothesis that endobronchial lesions of sarcoidosis in bronchi and bronchioles cause remodeling of the bronchial trees and airways. Further studies and reports are needed to clarify the pathology and etiology of bullous sarcoidosis.
Correspondence to: Shinji Teramoto, MD, FCCP, Department of Geriatric Medicine, Tokyo University Hospital, 7-3-1 Hongo Bunkyo-ku, Tokyo, Japan 113-8655
References
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