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dc.contributor.authorKurt, Gokhan
dc.contributor.authorAslan, Ayfer
dc.contributor.authorKara, Enes
dc.contributor.authorErol, Gokberk
dc.contributor.authorSahin, Merve Buke
dc.contributor.authorUcar, Murat
dc.date.accessioned2021-11-01T15:05:53Z
dc.date.available2021-11-01T15:05:53Z
dc.date.issued2021
dc.identifier.issn0303-8467
dc.identifier.issn1872-6968
dc.identifier.urihttps://doi.org/10.1016/j.clineuro.2020.106443
dc.identifier.urihttps://hdl.handle.net/11491/7432
dc.description.abstractBackground: Cerebral developmental venous anomalies (DVAs) are frequently diagnosed incidentally owing to the advances in neuroimaging. They are regarded as clinically insignificant due to their supposed quiescent existence which the authors aimed to contradict in this paper. Aim: In the aim of constituting a better understanding of clinical presentation of DVAs and making an estimation regarding the probability of resulting in a hemorrhage, the authors presented their experiences with a case series of DVAs. Methods: A retrospective analysis was carried out among patients who underwent brain MRI in a radiology department of a university between January of 2019 and January of 2020. Results: A total of 101 patients with DVA were extracted. 38 patients had isolated DVAs, while 63 patients had various accompanying cerebral pathologies, mostly cavernomas (39 patients) and AVMs (11 patients). The main complaints leading investigation were headache, dizziness, ataxia, nausea\vomiting, seizures and focal neurological deficits. 41 patients were truly symptomatic with indicative findings of seizures, neurological deficits or intracranial hemorrhages, and 12 of them had solitary DVAs. 22 patients presented with hemorrhages, and of them, 10 had only DVA, while the rest had some associated lesions, most often cavernoma. Of 22 patients with hemorrhage, 5 were operated, 5 were applied radiosurgery; while the rest were followed without any intervention. Conclusion: Although the symptoms in patients with DVA are generally charged on other associated pathologies, the fact that isolated DVAs may occasionally be problematic in the range of minor symptoms and severe hemorrhage should not be underestimated.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.ispartofClinical Neurology And Neurosurgeryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCerebral vascular malformationen_US
dc.subjectdevelopmental venous anomalyen_US
dc.subjecthemorrhageen_US
dc.subjectvenous angiomaen_US
dc.subjectvenous malformationen_US
dc.titleDifferent Aspects on Clinical Presentation of Developmental Venous Anomalies: Are They as Benign as Known? A Single Center Experienceen_US
dc.typearticleen_US
dc.department[Belirlenecek]en_US
dc.identifier.volume201en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Kurt, Gokhan; Kara, Enes; Erol, Gokberk; Ucar, Murat] Gazi Univ, Fac Med, Dept Neurosurg, Ankara, Turkey; [Aslan, Ayfer] Hitit Univ, Dept Neurosurg, Fac Med, Corum, Turkey; [Sahin, Merve Buke] Hacettepe Univ, Fac Med, Dept Publ Hlth, Ankara, Turkeyen_US
dc.contributor.institutionauthor[Belirlenecek]
dc.identifier.doi10.1016/j.clineuro.2020.106443
dc.description.wospublicationidWOS:000617810400015en_US
dc.description.scopuspublicationid2-s2.0-85098716571en_US
dc.description.pubmedpublicationidPubMed: 33388660en_US


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