Imaging conundrum – COVID-related lung changes or connective tissue disease-related interstitial lung disease

Dear Editor,
Coronavirus disease 2019 (COVID-19) pneumonia pre­sents with clinical features of variable severity. Imaging in the form of chest radiograph and high-resolution computed tomography (HRCT) play a central role in the management of patients suffering from COVID-19 pneumonia. The HRCT findings in such cases reflect the lung injury caused due to the viral pneumonia and the results of a cascade of inflammatory mediators. In the initial phase of the disease (day 1-6 of illness), changes are described as subpleural ground glass opacities and consolidation, either alone or in combination with inter­lobular septal lines, which may give rise to the “crazy paving appearance”. It is in the later phase of the disease (day 6-11 of illness) that the imaging appearance evolves into architectural distortion, perilobular opacities, and subpleural linear/curvilinear changes [1]. These appearances are similar to the imaging appearance of interstitial lung disease (ILD) patterns of organizing pneumonia (OP) and non-specific interstitial pneumonia (NSIP), which is an imaging conundrum. These imaging patterns are common HRCT findings in various connective tissue diseases (CTD)-related ILD. NSIP is the commonest pattern of CTD-related ILD, with systemic sclerosis being the archetype [2]. Rheumatoid arthritis (RA)-related ILD also shows an NSIP pattern, even though the pattern most frequently reported is the usual interstitial pneumonia (UIP). The OP pattern is commonly seen in dermatomyositis/polymyositis (PM/DM), and less commonly in RA, Sjögren syndrome, and systemic lupus erythematosus [3]. Because the presence of pre-existing ILD is a WHO-defined risk factor for severe affection of COVID-19, these patients often present with HRCT appearances of their pre-existing disease and overlapping features of COVID pneumonia. The differentiation between the two becomes especially challenging in a resource constrained setting, where prior imaging for comparison may not be readily available.
The HRCT appearance of NSIP is that of lower lobe, predominantly peripheral changes, which are ground glass opacities (GGO) without bronchiectasis in cellular NSIP; GGO with fine reticular changes, microcysts, areas of interlobular septal thickening, tractional bronchiectasis, and volume loss in the fibrotic NSIP. The subpleural sparing described as a chara­cteristic finding of NSIP, if absent, does not preclude the diagnosis. A lower lobar volume loss often accompanies...


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