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Published byHarjanti Sumadi Modified over 5 years ago
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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 (September 2011) DOI: /j.jaad Copyright © Terms and Conditions
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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 , DOI: ( /j.jaad ) Copyright © Terms and Conditions
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Fig 2 Chest computed tomography (CT) scan taken in May 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 , DOI: ( /j.jaad ) Copyright © Terms and Conditions
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