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, lea...

Olles dieđut

Bibliográfalaš dieđut

Váldodahkkit:	Baukje M. Zaaijer, Nienke Duppen, Brigitte W.M. Willemse, Martijn V. Verhagen, Marcus T.R. Roofthooft, Wim Timens, Rolf M.F. Berger, Johannes M. Douwes
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Elsevier 2021-01-01
Ráidu:	Respiratory Medicine Case Reports
Fáttát:	Outcome Hereditary hemorrhagic telangiectasia Pulmonary hypertension Pulmonary veno-occlusive disease Pediatrics Cardiology
Liŋkkat:	http://www.sciencedirect.com/science/article/pii/S2213007121002264
Fáddágilkorat:	Lasit fáddágilkoriid Eai fáddágilkorat, Lasit vuosttaš fáddágilkora!