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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Detalles Bibliográficos
Autores principales: Weatherald, Jason, Lategan, Johan, Helmersen, Doug
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927635/
https://www.ncbi.nlm.nih.gov/pubmed/27408785
http://dx.doi.org/10.1016/j.rmcr.2016.06.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927635/
https://www.ncbi.nlm.nih.gov/pubmed/27408785
http://dx.doi.org/10.1016/j.rmcr.2016.06.007

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