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Updated: Jun 25, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
[Dyspnea upon exertion in systemic scleroderma: from symptom to etiological diagnosis]
Eric Hachulla1, Jean François Bervar, David Launay
1Centre de référence des maladies auto-immunes et des maladies systémique rares sclérodermie systémique, Service de Médecine interne, Hôpital Claude Huriez, CHRU, F-59037 Lille Cedex, France. ehachulla@chru-lille.fr
Abstract:
Pulmonary hypertension and interstitial lung disease are the two main causes of death in systemic sclerosis. The hallmark of these complications is dyspnea on exertion. Assessment of dyspnea in systemic sclerosis is based on a questionnaire; 6-minute walk test and Borg index. After excluding anemia, a deceptive cause mainly due to digestive haemorrhage, echocardiography, pulmonary function tests and high resolution computed tomography of the chest are the first step to diagnosis. Peak velocity of tricuspid regurgitation as measured by echocardiography is the main parameter to evaluate the risk of pulmonary hypertension before performing a right heart catheterization. Diastolic left ventricle dysfunction is another frequently encountered cause of dyspnea in systemic sclerosis. Other less common causes are pericarditis, respiratory muscle involvement, lung cancer, pulmonary embolism.
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