1994
DOI: 10.1016/0090-3019(94)90030-2
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Vascular malformations of the brain in hereditary hemorrhagic telangiectasia (rendu-osler-weber disease)

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Cited by 81 publications
(61 citation statements)
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“…The process often produces degenerative weakening within the wall of these vessels, predisposing to rupture. Although the natural history of sporadic cerebral AVM has been well documented, the specific natural course of the cerebral AVM in HHT is not known 23 .…”
Section: Discussionmentioning
confidence: 99%
“…The process often produces degenerative weakening within the wall of these vessels, predisposing to rupture. Although the natural history of sporadic cerebral AVM has been well documented, the specific natural course of the cerebral AVM in HHT is not known 23 .…”
Section: Discussionmentioning
confidence: 99%
“…They form a part of syndromes such as Rendu-Osler-Weber or Klippel-Trenaunay-Weber syndrome, consistent with the fact that a genetic abnormality contributes to their etiology. 5,13,18 Acquired pial AVFs are very rare and are the result of traumatic injury or iatrogenic causes. Our patient had a minor head injury, but it was difficult to identify whether this head injury was the cause of the pial AVF from her initial CT scan.…”
Section: Discussionmentioning
confidence: 99%
“…Intracranial pial AVFs are composed of one or more direct arterial shunt to a sole venous channel without abnormal interconnecting nidus, which differentiate from AVMs for the absence of nidus and dural AVFs for the feeding vessels originated from pial or cortical arteries and located outside of the dural leaflets (4,12). The high and turbulent blood flow hemodynamics of pial AVFs result from arteriovenous shunt from feeding arteries directly into single draining vein, which result in venous dilatation, varix and even the aneurysm of the feeding artery (8,10).…”
Section: Discussionmentioning
confidence: 99%