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Pulmonary arterial hypertension secondary to adult-onset Still’s disease: Response to cyclosporine and sildenafil over 15 years of follow-up

Adult onset Still’s disease (AOSD) is an autoimmune disease characterized by systemic inflammation and is a rarely reported cause of pulmonary arterial hypertension (PAH). We describe the clinical course of a 40-year-old woman who presented with PAH 19 months after a diagnosis of AOSD. Sildenafil an...

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Bibliographic Details
Published in:Respir Med Case Rep
Main Authors: Weatherald, Jason, Lategan, Johan, Helmersen, Doug
Format: Artigo
Language:Inglês
Published: Elsevier 2016
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4927635/
https://ncbi.nlm.nih.gov/pubmed/27408785
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2016.06.007
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