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Total endovascular occlusion of a giant direct arteriovenous fistula in the posterior fossa in a case of Rendu-Osler-Weber disease
We report a case of giant single-hole direct arteriovenous fistula (AVF) located in the posterior fossa of a child with Rendu-Osler-Weber disease (ROW). There is neither a clinical nor an angioarchitectural difference between AVFs associated with ROW and sporadic AVFs, but ROW should be suspected in...
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Published in: | Child's nervous system 1996-12, Vol.12 (12), p.785-788 |
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container_title | Child's nervous system |
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creator | COUBES, P HUMBERTCLAUDE, V RODESCH, G LASJAUNIAS, P ECHENNE, B FREREBEAU, P |
description | We report a case of giant single-hole direct arteriovenous fistula (AVF) located in the posterior fossa of a child with Rendu-Osler-Weber disease (ROW). There is neither a clinical nor an angioarchitectural difference between AVFs associated with ROW and sporadic AVFs, but ROW should be suspected in children with multifocal pial AVFs. Transarterial embolization was performed to obliterate the AVF in a unique procedure using simultaneous bifemoral catheterization. At follow up 4 years later, the clinical examination was normal. Control MR scans and angiography showed the total occlusion of the fistula, permanent thrombosis of the venous pouch, and disappearance of the abnormal venous drainage. In this case, the endovascular procedure was available and we estimated that it represented a lesser risk than the surgical approach (risk of hemorrhage and risk of thrombosis involving the feeding arteries and the brain stem venous drainage). Furthermore, it avoids craniotomy and reduces the duration of hospitalization. |
doi_str_mv | 10.1007/bf00261599 |
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There is neither a clinical nor an angioarchitectural difference between AVFs associated with ROW and sporadic AVFs, but ROW should be suspected in children with multifocal pial AVFs. Transarterial embolization was performed to obliterate the AVF in a unique procedure using simultaneous bifemoral catheterization. At follow up 4 years later, the clinical examination was normal. Control MR scans and angiography showed the total occlusion of the fistula, permanent thrombosis of the venous pouch, and disappearance of the abnormal venous drainage. In this case, the endovascular procedure was available and we estimated that it represented a lesser risk than the surgical approach (risk of hemorrhage and risk of thrombosis involving the feeding arteries and the brain stem venous drainage). 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HUMBERTCLAUDE, V ; RODESCH, G ; LASJAUNIAS, P ; ECHENNE, B ; FREREBEAU, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-cb8ef123434d74a39a3e19609332df4e02dd0a1fb45661c147da9ebb882a6d463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Cerebral Angiography</topic><topic>Cranial Fossa, Posterior - blood supply</topic><topic>Embolization, Therapeutic</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Intracranial Arteriovenous Malformations - diagnosis</topic><topic>Intracranial Arteriovenous Malformations - genetics</topic><topic>Intracranial Arteriovenous Malformations - therapy</topic><topic>Magnetic Resonance Imaging</topic><topic>Medical sciences</topic><topic>Neurologic Examination</topic><topic>Neurology</topic><topic>Telangiectasia, Hereditary Hemorrhagic - diagnosis</topic><topic>Telangiectasia, Hereditary Hemorrhagic - genetics</topic><topic>Telangiectasia, Hereditary Hemorrhagic - therapy</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>COUBES, P</creatorcontrib><creatorcontrib>HUMBERTCLAUDE, V</creatorcontrib><creatorcontrib>RODESCH, G</creatorcontrib><creatorcontrib>LASJAUNIAS, P</creatorcontrib><creatorcontrib>ECHENNE, B</creatorcontrib><creatorcontrib>FREREBEAU, P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>COUBES, P</au><au>HUMBERTCLAUDE, V</au><au>RODESCH, G</au><au>LASJAUNIAS, P</au><au>ECHENNE, B</au><au>FREREBEAU, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Total endovascular occlusion of a giant direct arteriovenous fistula in the posterior fossa in a case of Rendu-Osler-Weber disease</atitle><jtitle>Child's nervous system</jtitle><addtitle>Childs Nerv Syst</addtitle><date>1996-12-01</date><risdate>1996</risdate><volume>12</volume><issue>12</issue><spage>785</spage><epage>788</epage><pages>785-788</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>We report a case of giant single-hole direct arteriovenous fistula (AVF) located in the posterior fossa of a child with Rendu-Osler-Weber disease (ROW). There is neither a clinical nor an angioarchitectural difference between AVFs associated with ROW and sporadic AVFs, but ROW should be suspected in children with multifocal pial AVFs. Transarterial embolization was performed to obliterate the AVF in a unique procedure using simultaneous bifemoral catheterization. At follow up 4 years later, the clinical examination was normal. Control MR scans and angiography showed the total occlusion of the fistula, permanent thrombosis of the venous pouch, and disappearance of the abnormal venous drainage. In this case, the endovascular procedure was available and we estimated that it represented a lesser risk than the surgical approach (risk of hemorrhage and risk of thrombosis involving the feeding arteries and the brain stem venous drainage). 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subjects | Adolescent Biological and medical sciences Cerebral Angiography Cranial Fossa, Posterior - blood supply Embolization, Therapeutic Female Follow-Up Studies Humans Intracranial Arteriovenous Malformations - diagnosis Intracranial Arteriovenous Malformations - genetics Intracranial Arteriovenous Malformations - therapy Magnetic Resonance Imaging Medical sciences Neurologic Examination Neurology Telangiectasia, Hereditary Hemorrhagic - diagnosis Telangiectasia, Hereditary Hemorrhagic - genetics Telangiectasia, Hereditary Hemorrhagic - therapy Vascular diseases and vascular malformations of the nervous system |
title | Total endovascular occlusion of a giant direct arteriovenous fistula in the posterior fossa in a case of Rendu-Osler-Weber disease |
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