Abstract
Determining whether an “idiopathic” interstitial pneumonia (IP) is actually a manifestation of an underlying connective tissue disease (CTD) is important, because this knowledge often has a significant impact on management and prognosis. The detection of occult CTD (and distinguishing these cases from idiopathic disease) is challenging and can be optimized by a thorough and multidisciplinary evaluation. In this chapter, we discuss the complex intersection that exists between CTD and interstitial lung disease (ILD) and highlight specific clinical, laboratory, radiologic, and histopathologic features that are useful in distinguishing CTD-associated ILD from idiopathic interstitial pneumonia (IIP).
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Solomon, J.J., Fischer, A. (2014). Idiopathic Interstitial Pneumonia and Connective Tissue Disease-Associated Interstitial Lung Disease: Similarities and Differences. In: Meyer, K., Nathan, S. (eds) Idiopathic Pulmonary Fibrosis. Respiratory Medicine, vol 9. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-682-5_11
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DOI: https://doi.org/10.1007/978-1-62703-682-5_11
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