Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/6954
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Oran, I. | - |
dc.contributor.author | Kiroglu, Y. | - |
dc.contributor.author | Yurt, A. | - |
dc.contributor.author | Ozer, F.D. | - |
dc.contributor.author | Acar, Feridun | - |
dc.contributor.author | Dalbasti, T. | - |
dc.contributor.author | Yagci, B. | - |
dc.date.accessioned | 2019-08-16T12:13:29Z | - |
dc.date.available | 2019-08-16T12:13:29Z | - |
dc.date.issued | 2009 | - |
dc.identifier.issn | 0028-3940 | - |
dc.identifier.uri | https://hdl.handle.net/11499/6954 | - |
dc.identifier.uri | https://doi.org/10.1007/s00234-008-0456-9 | - |
dc.description.abstract | Introduction: To examine the clinical and radiologic findings of patients with developmental venous anomaly (DVA) associated with intracranial haemorrhage but unrelated to cavernoma. Methods: Computed tomography (CT) was used to obtain intracranial images from seven patients ranging in age from 6 to 51 years. Magnetic resonance imaging (MRI) was then performed on six patients, and two patients were further examined via CT angiography. Finally, digital subtraction angiography (DSA) was performed to confirm the initial diagnosis. Results: CT showed intraparenchymal supratentorial haemorrhage in all patients. The combined imaging modalities eventually confirmed a diagnosis of arterialised DVA in four patients and arterialised DVA associated with arteriovenus malformation (AVM) in three. Two patients were managed symptomatically, two underwent radiosurgery, one underwent surgery, one underwent combined embolisation plus radiosurgery and the remaining patient underwent combined embolisation plus surgery. Two patients died, one as a result of re-bleeding, and the other due to radiation necrosis. The mean follow-up period was 33 months (6 months to 6 years) for the remaining five patients with favourable outcome. Conclusion: DVA associated with intraparenchymal haemorrhage, but not related to cavernoma, was confirmed. Though very rare, DVA may present with non-cavernoma-related haemorrhage in the form of arterialised DVA or DVA with AVM. © 2008 Springer-Verlag. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Neuroradiology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Arteriovenous malformation | en_US |
dc.subject | Developmental venous anomaly | en_US |
dc.subject | Digital subtraction angiography | en_US |
dc.subject | Embolisation | en_US |
dc.subject | Intracranial bleeding | en_US |
dc.subject | adolescent | en_US |
dc.subject | adult | en_US |
dc.subject | article | en_US |
dc.subject | artificial embolism | en_US |
dc.subject | bleeding | en_US |
dc.subject | brain angiography | en_US |
dc.subject | brain arteriovenous malformation | en_US |
dc.subject | brain decompression | en_US |
dc.subject | brain hemorrhage | en_US |
dc.subject | brain radiography | en_US |
dc.subject | brain surgery | en_US |
dc.subject | brain tumor | en_US |
dc.subject | clinical article | en_US |
dc.subject | clinical feature | en_US |
dc.subject | computed tomographic angiography | en_US |
dc.subject | contrast enhancement | en_US |
dc.subject | controlled study | en_US |
dc.subject | craniotomy | en_US |
dc.subject | developmental disorder | en_US |
dc.subject | digital subtraction angiography | en_US |
dc.subject | female | en_US |
dc.subject | follow up | en_US |
dc.subject | gamma knife radiosurgery | en_US |
dc.subject | human | en_US |
dc.subject | male | en_US |
dc.subject | nuclear magnetic resonance imaging | en_US |
dc.subject | preschool child | en_US |
dc.subject | priority journal | en_US |
dc.subject | radiation necrosis | en_US |
dc.subject | treatment outcome | en_US |
dc.subject | Adolescent | en_US |
dc.subject | Adult | en_US |
dc.subject | Angiography, Digital Subtraction | en_US |
dc.subject | Brain | en_US |
dc.subject | Cerebral Angiography | en_US |
dc.subject | Cerebral Veins | en_US |
dc.subject | Child | en_US |
dc.subject | Diagnosis, Differential | en_US |
dc.subject | Female | en_US |
dc.subject | Humans | en_US |
dc.subject | Intracranial Hemorrhages | en_US |
dc.subject | Magnetic Resonance Imaging | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Retrospective Studies | en_US |
dc.subject | Tomography, X-Ray Computed | en_US |
dc.subject | Treatment Outcome | en_US |
dc.subject | Young Adult | en_US |
dc.title | Developmental venous anomaly (DVA) with arterial component: A rare cause of intracranial haemorrhage | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 51 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 25 | - |
dc.identifier.startpage | 25 | en_US |
dc.identifier.endpage | 32 | en_US |
dc.identifier.doi | 10.1007/s00234-008-0456-9 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 18787814 | en_US |
dc.identifier.scopus | 2-s2.0-57849089075 | en_US |
dc.identifier.wos | WOS:000261791400004 | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale University | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.grantfulltext | none | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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