Complete resolution of apparently definite radiological and histological usual interstitial pneumonia

Simon, D. ; Irusen, E. M. ; Allwood, B. W. ; Rigby, J. ; Koegelenberg, C. F. N. (2018-08-30)

CITATION: Simon, D. et al. 2018. Complete resolution of apparently definite radiological and histological usual interstitial pneumonia. South African Medical Journal, 108(9):726-728, doi:10.7196/SAMJ.2018.v108i9.13335.

The original publication is available at http://www.samj.org.za

Article

ENGLISH ABSTRACT: Idiopathic pulmonary fibrosis is considered to be the most common form of pulmonary fibrosis. It is a progressive and irreversible disease with a reported median survival of ~3 years. The pathological correlate is usual interstitial pneumonia (UIP), and although antifibrotic agents can slow down lung function decline, they do not completely reverse the disease process. To date, there have been no case reports describing reversal of UIP. We present a case where both the imaging and histology were compatible with definite UIP, yet it reversed with immunosuppressive therapy without the use of antifibrotic agents.

Please refer to this item in SUNScholar by using the following persistent URL: http://hdl.handle.net/10019.1/106738
This item appears in the following collections: