| Literature DB >> 27504339 |
Mohan Rao Kotnur1, Parinita Suresh2, Venkata Siva Prasad Reddy2, Tarun Sharma2, Nabil Ahmed Salim2.
Abstract
Systemic sclerosis (SSc) is a chronic autoimmune multisystem disorder characterized by endothelial dysfunction and fibroblast dysfunction, which results in progressive fibrosis of the skin and internal organs more frequently the lungs and gastro intestinal tract. Pulmonary involvement is common in the course of SSc, with Interstitial Lung Disease (ILD) and Pulmonary Arterial Hypertension (PAH) being the leading causes of death. Here we report, case of an elderly female patient presenting with Diffuse SSc with multiple uncommon pulmonary manifestations like ILD with Usual Interstitial Pneumonia (UIP) pattern (usually less common), PAH and right sided pleural effusion.Entities:
Keywords: Interstitial lung disease; Pulmonary arterial hypertension; Scleroderma; Usual interstitial pneumonia
Year: 2016 PMID: 27504339 PMCID: PMC4963699 DOI: 10.7860/JCDR/2016/18781.8032
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X