Rare Case of Reversible Pulmonary Arterial Hypertension Secondary to Cyclophosphamide and Doxorubicin Chemotherapy

Pulmonary arterial hypertension (PAH), characterized as a resting mean pulmonary artery pressure greater than 25 mmHg, is due to the narrowing of the pulmonary arteries, which can be idiopathic, inherited, or drug-related. Alkylating agents, including cyclophosphamide, are a risk factor for developi...

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Detalles Bibliográficos
Autores principales: Javed, Aneeqa, Medina, Yelizaveta, Bux, Amber, Sahra, Syeda, Rojas-Marte, Geurys
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Cardiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306451/
https://www.ncbi.nlm.nih.gov/pubmed/35891814
http://dx.doi.org/10.7759/cureus.26207

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306451/
https://www.ncbi.nlm.nih.gov/pubmed/35891814
http://dx.doi.org/10.7759/cureus.26207

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