Pulmonary arterial hypertension associated with pulmonary arteriovenous malformations and pulmonary veno-occlusive disease: A devastating combination

We describe a case of an adolescent male with the rare combination of pulmonary arterial hypertension (PAH) and pulmonary arteriovenous malformations (PAVM's) without confirmed hereditary hemorrhagic telangiectasia (HHT). The patient showed clinical deterioration on standard vasodilator therapy...

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Detalles Bibliográficos
Autores principales: Zaaijer, Baukje M., Duppen, Nienke, Willemse, Brigitte W.M., Verhagen, Martijn V., Roofthooft, Marcus T.R., Timens, Wim, Berger, Rolf M.F., Douwes, Johannes M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654615/
https://www.ncbi.nlm.nih.gov/pubmed/34934615
http://dx.doi.org/10.1016/j.rmcr.2021.101564

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654615/
https://www.ncbi.nlm.nih.gov/pubmed/34934615
http://dx.doi.org/10.1016/j.rmcr.2021.101564

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