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Erschienen in: Lung 4/2007

01.08.2007 | Book Review

Interstitial Lung Disease in Systemic Sclerosis

verfasst von: Predrag Ostojic, Marco Matucci Cerinic, Richard Silver, Kristin Highland, Nemanja Damjanov

Erschienen in: Lung | Ausgabe 4/2007

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Abstract

We reviewed the literature concerning pathogenesis, clinical features, diagnosis and treatment of interstitial lung disease (ILD) in patients with systemic sclerosis (SSc). ILD is detectable in approximately 70% of patients at autopsy. Nonspecific interstitial pneumonia (NSIP) is the most common pathologic finding. The earliest phase of ILD in SSc is characterized by microvascular injury and alveolitis. Endothelial lesions, activation of coagulation proteases, especially thrombin, fibroblast proliferation, and differentiation of normal lung fibroblasts to a myofibroblasts phenotype are hallmarks of ILD in SSc. Diagnostic procedures used to detect ILD are chest X-ray, high-resolution computed tomography, bronchoalveolar lavage, lung function tests, and sometimes thoracoscopic lung biopsy. Novel and potentially useful methods to diagnose ILD in SSc are induced sputum and technetium-labeled diethylenetriamine pentaacetate (99mTC-DTPA) clearance time. Cyclophosphamide seems to be relatively effective to treat ILD in the earliest phase, but the effects of other immunosuppressive drugs on the lungs are less convincing.
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Metadaten
Titel
Interstitial Lung Disease in Systemic Sclerosis
verfasst von
Predrag Ostojic
Marco Matucci Cerinic
Richard Silver
Kristin Highland
Nemanja Damjanov
Publikationsdatum
01.08.2007
Verlag
Springer-Verlag
Erschienen in
Lung / Ausgabe 4/2007
Print ISSN: 0341-2040
Elektronische ISSN: 1432-1750
DOI
https://doi.org/10.1007/s00408-007-9012-3

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