Results 41 to 50 of about 6,864 (154)

Case report: Embolization of Traumatic Pulmonary Arteriovenous Malformation Due to Inferior Phrenic Artery Supply

open access: yesSaudi Journal of Radiology
Pulmonary arteriovenous malformations (PAVMs) can arise from various underlying conditions and can present with hemoptysis, necessitating prompt emergency medical intervention.
Ibrahim Aljediea   +4 more
doaj   +1 more source

Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports

open access: yesBMC Neurology, 2011
Background Paradoxical embolism due to pulmonary arteriovenous malformations is the main mechanism of brain infarction in patients with hereditary hemorrhagic telangiectasia.
Viader Fausto   +4 more
doaj   +1 more source

Orthodeoxia without Platypnea in Hereditary Hemorrhagic Telangiectasia in the Presence of a Cerebral Abscess and Multiple Pulmonary Arteriovenous Malformations: Unusual Complications and Transcatheter Endovascular Treatment

open access: yesCase Reports in Pulmonology, 2017
Hereditary hemorrhagic telangiectasia is a rare autosomal-dominant condition affecting visceral blood vessel development. Cerebral and most commonly pulmonary arteriovenous malformations are found in the majority of symptomatic patients.
Carlos Salazar   +2 more
doaj   +1 more source

Device closure of pulmonary arteriovenous malformation using Amplatzer vascular plug II in hereditary hemorrhagic telangiectasia

open access: yesIndian Heart Journal, 2015
Pulmonary arteriovenous malformations (AVM) are very rare and carry the risk of cerebral thrombo-embolism, brain abscess or pulmonary hemorrhage. The Amplatzer vascular plug II (AVP II) is a new device, used for embolization of the pulmonary AVMs.
Gopalan Nair Rajesh   +5 more
doaj   +1 more source

Pulmonary Arteriovenous Malformation [PDF]

open access: yesDeutsches Ärzteblatt international, 2019
Manuel, Klein   +2 more
openaire   +3 more sources

Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

open access: yesRespiratory Medicine Case Reports, 2020
Pulmonary arteriovenous malformations (PAVM) are generally congenital lesions caused by abnormal capillary development. Lesions can be in the form of isolated anomaly or as part of autosomal dominantly inherited hereditary hemorrhagic telengiectasia (HHT)
Saniye Girit   +3 more
doaj   +1 more source

Malformações arteriovenosas pulmonares: Associação a telangiectasia hemorrágica hereditária Casos clínicos e rastreio familiar Pulmonary arteriovenous malformations: Association with hereditary hemorrhagic telangiectasia. Clinical cases and family screening

open access: yesRevista Portuguesa de Pneumologia, 2006
As malformações arteriovenosas pulmonares são raras e mais de metade dos casos surgem em associação a telangiectasia hemorrágica hereditária. Faz-se uma revisão teórica sobre a apresentação clínica, abordagem diagnóstica, terapêutica e prognóstico destas
Diva Ferreira   +5 more
doaj  

Pulmonary Arteriovenous Malformation can be Associated with Embolic Stroke of Undetermined Source (ESUS)

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2019
Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies. Alternative designations are pulmonary arteriovenous fistulae or aneurysms. Although mostly asymptomatic, PAVMs can cause respiratory symptoms due to right-to-left shunt.
Mariana Barros Cruz   +3 more
doaj   +1 more source

Giant pulmonary arteriovenous malformations

open access: yesCase Reports in Clinical Practice, 2016
No ...
Farnoosh Larti   +3 more
doaj  

Detachable coiling for embolotherapy of high-flow pulmonary arteriovenous malformation: case report and review of the literature

open access: yesJournal of the Belgian Society of Radiology, 2010
Pulmonary arteriovenous malformations (PAVMs) are very rare anomalies of the lung parenchyma. Although many patients are asymptomatic, it carries a high risk of severe cerebral complications, and rarely fatal outcome due to rupture of the malformation ...
M Laureys, P Mendes da Costa, L Divano
doaj   +1 more source

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