Interstitial Lung Disease in a Patient with Dyskeratosis Congenita

Title
Interstitial Lung Disease in a Patient with Dyskeratosis Congenita
Author(s)
정진홍이관호신경철현명수김기홍김현정[김현정]김규진[김규진]
Keywords
Lung Diseases; Interstitial; Dyskeratosis Congenita; Anemia; Aplastic
Issue Date
201302
Publisher
대한결핵및호흡기학회
Citation
Tuberculosis and Respiratory Diseases, v.74, no.2, pp.70 - 73
Abstract
Dyskeratosis congenita is a rare congenital disorder characterized by a triad of reticular pigmentation of the skin, dystrophic nails, and leukoplakia of the mucous membrane. Sometimes it is associated with bone marrow failure,secondary malignancy and interstitial lung disease. Though it is rare, Dyskeratosis congenita is diagnosed relatively easily when clinicians suspect it. It can be diagnosed just by gross inspection with care. Dyskeratosis congenita should be considered as one cause associated with interstitial lung disease. In Korea, interstitial lung disease with dyskeratosis congenita has not been reported. We report a case and review the literature.
URI
http://hdl.handle.net/YU.REPOSITORY/26360
ISSN
1738-3536
Appears in Collections:
의과대학 > 내과학교실 > Articles
의과대학 > 피부과학교실 > Articles
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