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Background: Systemic sclerosis (SSc) is an autoimmune connective tissue disorder causing microvascular abnormality leading to Raynaud's phenomenon, skin tightening, and nailfold capillary changes. The patient may have systemic involvement, among them interstitial lung disease (ILD) and pulmonary arterial hypertension are mainly associated with disease-related mortality. Aims: To find out an association between nailfold capillaroscopic changes with ILD severity. Materials and Methods: An institution based cross-sectional study was performed among the patients of SSc above 18 years. Detailed history was taken. Clinical examinations, nailfold capillaroscopy (NFC) with a dermatoscope and high-resolution computed tomography (HRCT) scan of thorax were done. Data were analyzed in MedCalc statistical software version 20. Results: Out of total 43 patients, 74.4% ( n = 32) were female. Mean age was 35.05 ± 7.24 years and mean duration 4.28 ± 2.81 years. Diffuse SSc was found in 88.37% ( n = 38). On NFC, early, active, and late patterns were found in 30.2% ( n = 13), 25.6% ( n = 11), and 44.2% ( n = 19) cases, respectively. On HRCT, early, active, and late ILD were present in 18.6% ( n = 8), 37.2% ( n = 16), and 30.2% ( n = 13) cases, respectively. ILD changes were absent in 14% ( n = 6) though NFC changes were present in them. Respiratory symptoms were absent in 20.93% ( n = 9) patients though all had features of early NFC and among them 9.3% ( n = 4) showed early ILD changes on HRCT. Significant associations were found between NFC changes and ILD severity ( P = 0.0003), NFC changes and respiratory symptoms ( P < 0.0001) and between ILD changes and respiratory symptoms ( P < 0.0001). Discussion: NFC, an inexpensive procedure, can be performed in all patients of SSc to detect development of early ILD even before appearance of respiratory symptoms to prevent further progression.

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