SciELO - Scientific Electronic Library Online

 
vol.108 issue9We are tired of 'adrenal fatigue'Leveraging the Road to Health booklet as a unique patient identifier to monitor the prevention of mother-to-child transmission programme author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Article

Indicators

Related links

  • On index processCited by Google
  • On index processSimilars in Google

Share


SAMJ: South African Medical Journal

On-line version ISSN 2078-5135
Print version ISSN 0256-9574

Abstract

SIMON, D et al. Complete resolution of apparently definite radiological and histological usual interstitial pneumonia. SAMJ, S. Afr. med. j. [online]. 2018, vol.108, n.9, pp.726-728. ISSN 2078-5135.  http://dx.doi.org/10.7196/samj.2018.v108i9.13335.

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.

        · text in English     · English ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License