نتایج جستجو برای: pulmonary malformations

تعداد نتایج: 241369  

2004
Y-L Hsu H-C Wang P-C Yang

Cerebral manifestations of Osler-Weber-Rendu disease (OWRD, hereditary haemorrhagic telangiectasia) including telangiectases, venous malformations, and arteriovenous malformations, are usually under-recognised. The highest complication rate is observed in high flow cerebral arteriovenous malformations, which may present with headache, epilepsy, ischaemia, or haemorrhage. Cerebral air embolism d...

Journal: :British journal of sports medicine 2004
Y-L Hsu H-C Wang P-C Yang

Cerebral manifestations of Osler-Weber-Rendu disease (OWRD, hereditary haemorrhagic telangiectasia) including telangiectases, venous malformations, and arteriovenous malformations, are usually under-recognised. The highest complication rate is observed in high flow cerebral arteriovenous malformations, which may present with headache, epilepsy, ischaemia, or haemorrhage. Cerebral air embolism d...

Journal: :The Cochrane database of systematic reviews 2010
Charlie C-T Hsu Gigi Nc Kwan Shane A Thompson Mieke L van Driel

BACKGROUND Pulmonary arteriovenous malformations are abnormal direct connections between the pulmonary artery and pulmonary vein which result in a right-to-left shunt. They are associated with substantial morbidity and mortality mainly from the effects of paradoxical emboli. Potential complications include stroke, cerebral abscess, pulmonary haemorrhage and hypoxaemia. Embolisation therapy is a...

2015
Hadi Rokni Yazdi Hamidreza Abtahi Hazhir Saberi Mona Salahi

Pulmonary arteriovenous malformations (AVMs) are rare vascular malformations of the lung that usually led to a notable risk of serious and life-threatening complications. There is considerable debate about the best management of strategies for the group of patients with diffuse AVMs. Several therapeutic options have been reported for management of this abnormality among which coil embolization ...

Journal: :Circulation 2001
H Justino L N Benson R M Freedom

Afemale child with visceral heterotaxy (presumed left isomerism), interrupted inferior vena cava with azygos continuation to the superior vena cava, and double-outlet right ventricle underwent a total cavopulmonary anastomosis (end-to-side anastomosis of the superior vena cava to the right pulmonary artery) in infancy. Completion of Fontan circulation was undertaken at 3 years of age with const...

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