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Curr Probl Diagn Radiol ; 51(3): 375-391, 2022.
Article in English | MEDLINE | ID: mdl-33827770

ABSTRACT

Osler-Weber-Rendu, also known as Hereditary Hemorrhagic Telangiectasia, is an autosomal dominant disease with phenotypic manifestations that include pulmonary, cerebrospinal, hepatic, and other visceral arteriovenous malformations (AVMs). Pulmonary AVMs can result in hypoxemia, hemoptysis, or stroke due to paradoxical embolism. The mainstay of treatment is transcatheter embolization. Central nervous system and abdominal visceral AVMs contribute to morbidity of the disease. Radiologists should be familiar with the imaging manifestations and treatment algorithm of AVMs in Osler-Weber-Rendu to effectively guide patient care.


Subject(s)
Arteriovenous Fistula , Arteriovenous Malformations , Pulmonary Veins , Telangiectasia, Hereditary Hemorrhagic , Arteriovenous Malformations/diagnostic imaging , Arteriovenous Malformations/therapy , Humans , Pulmonary Veins/abnormalities , Radiologists , Telangiectasia, Hereditary Hemorrhagic/complications , Telangiectasia, Hereditary Hemorrhagic/diagnostic imaging , Telangiectasia, Hereditary Hemorrhagic/therapy
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