Acceleration of pulmonary interstitial fibrosis in a patient with myeloperoxidase- antineutrophil cytoplasmic antibody-positive erythema elevatum diutinum

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Acceleration of pulmonary interstitial fibrosis in a patient with myeloperoxidase- antineutrophil cytoplasmic antibody-positive erythema elevatum diutinum Tamihiro Kawakami, MD, PhD, Mikiko Kyoya, MD, Shin Matsuoka, MD, PhD, Yoshinao Soma, MD, PhD Journal of the American Academy of Dermatology Volume 65, Issue 3, Pages 674-675 (September 2011) DOI: 10.1016/j.jaad.2010.06.052 Copyright © 2010 Terms and Conditions

Fig 1 High-resolution computed tomography scan demonstrates symmetric bilateral patchy areas of ground-glass opacity with traction bronchiectasis and bronchiolectasis. Findings suggest progression of pulmonary interstitial fibrosis (images taken in November 2009). Journal of the American Academy of Dermatology 2011 65, 674-675DOI: (10.1016/j.jaad.2010.06.052) Copyright © 2010 Terms and Conditions

Fig 2 Chest computed tomography (CT) scan taken in May 2005. CT scans taken 5 years apart show mild patchy ground-glass opacity. Findings suggest early pulmonary interstitial fibrosis. Journal of the American Academy of Dermatology 2011 65, 674-675DOI: (10.1016/j.jaad.2010.06.052) Copyright © 2010 Terms and Conditions