Percutaneous embolization of pulmonary arteriovenous malformations in adult patient with Rendu–Osler–Weber: a case report

BACKGROUND: Hereditary haemorrhagic telangiectasia (HHT), or Rendu–Osler–Weber syndrome, is a rare genetic disorder characterized by the development of telangiectasias and arteriovenous malformations (AVMs) throughout the body. We present a case of percutaneous embolization of pulmonary AVMs in an a...

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Detalles Bibliográficos
Autores principales: Schutyser, Wouter, Budts, Werner, Verhamme, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639099/
https://www.ncbi.nlm.nih.gov/pubmed/37954570
http://dx.doi.org/10.1093/ehjcr/ytad533

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639099/
https://www.ncbi.nlm.nih.gov/pubmed/37954570
http://dx.doi.org/10.1093/ehjcr/ytad533

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