An analysis of lesions associated with developmental venous anomalies
dc.authorid | Kantarcı, Mecit/0000-0002-1043-6719 | |
dc.authorwosid | Kantarcı, Mecit/HLQ-6851-2023 | |
dc.contributor.author | Taydaş, Onur | |
dc.contributor.author | Oğul, Hayri | |
dc.contributor.author | Kantarcı, Mecit | |
dc.date.accessioned | 2023-07-26T11:57:17Z | |
dc.date.available | 2023-07-26T11:57:17Z | |
dc.date.issued | 2021 | |
dc.department | DÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Radyoloji Ana Bilim Dalı | en_US |
dc.description.abstract | Objective The aim of this study was to describe different lesions and features associated with developmental venous anomalies (DVAs). Methods The records and magnetic resonance imaging (MRI) images of 1,722 patients who underwent cranial MRI between 2010 and 2017 were retrospectively reviewed. It was found that 124 (7.2%) patients had DVAs, and 48 of these patients (38.7%) had additional anomalies accompanying DVAs. Of the patients with DVAs, 25 were female and 23 were male, with a mean age of 39.3 years (range, 3-77 years). MRI was performed in all the patients. Results In addition to DVAs, cavernomas were present in 30 patients (62.5%), haematomas in 7 (14.5%), gliosis in 6 (12.5%), demyelinating plaques in 4 (8.3%) and a glioblastoma in 1 (2.2%). The mean diameter of the DVAs was 1.1mm and the mean diameter of the lesions was 17.4mm. The susceptibility weighted imaging (SWI) sequence was also applied to 12 patients with cavernomas. The relevant sequence in all of these patients contributed to the diagnosis. Conclusion Our study shows that DVAs can accompany a wide spectrum of lesions, especially cavernomas. Although their pathophysiology has not yet been clearly established, these lesions may have a common aetiology. | en_US |
dc.identifier.doi | 10.1308/rcsann.2021.0121 | |
dc.identifier.endpage | 774 | en_US |
dc.identifier.issn | 0035-8843 | |
dc.identifier.issn | 1478-7083 | |
dc.identifier.issue | 10 | en_US |
dc.identifier.pmid | 34448641 | en_US |
dc.identifier.scopus | 2-s2.0-85121402299 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 768 | en_US |
dc.identifier.uri | https://doi.org/10.1308/rcsann.2021.0121 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/13108 | |
dc.identifier.volume | 103 | en_US |
dc.identifier.wos | WOS:000810116100013 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.institutionauthor | Oğul, Hayri | |
dc.language.iso | en | en_US |
dc.publisher | Royal Coll Surgeons England | en_US |
dc.relation.ispartof | Annals of The Royal College of Surgeons of England | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.snmz | $2023V1Guncelleme$ | en_US |
dc.subject | Developmental Venous Anomaly; Cavernoma; Magnetic Resonance Imaging | en_US |
dc.subject | Multiple-Sclerosis; Brain; Abnormalities; Malformations; Prevalence; Hemorrhage; Children; Angioma; History | en_US |
dc.title | An analysis of lesions associated with developmental venous anomalies | en_US |
dc.type | Article | en_US |
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