The role of nuclear medicine in a case of Rendu–Osler–Weber disease with pulmonary involvement

Rendu–Osler–Weber syndrome or hereditary hemorrhagic telangiectasia (HHT) is a rare systemic disease. Its primary pathogenic expression is multiple arteriovenous malformations (AVM) and severe hypoxia. A case of suspected pulmonary embolism in a 49-year-old male with intestinal, cardiac, and pulmona...

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Detalles Bibliográficos
Autores principales: Barral, Carlyle Marques, Nunes, Isabella Correa Chaves, Nunes, Shirleide Santos, Sanches, Sandra Monetti Dumont
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686737/
https://www.ncbi.nlm.nih.gov/pubmed/35018158
http://dx.doi.org/10.4103/wjnm.wjnm_48_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686737/
https://www.ncbi.nlm.nih.gov/pubmed/35018158
http://dx.doi.org/10.4103/wjnm.wjnm_48_21

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