دورية أكاديمية

Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage - a rare occurrence

التفاصيل البيبلوغرافية
العنوان: Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage - a rare occurrence
المؤلفون: Marzouk, Omar, Marzouk, Sherief, Liyanage, Sidath H, Grunwald, Iris Q
المصدر: Marzouk , O , Marzouk , S , Liyanage , S H & Grunwald , I Q 2021 , ' Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage - a rare occurrence ' , Radiology case reports , vol. 16 , no. 6 , pp. 1463-1468 . https://doi.org/10.1016/j.radcr.2021.03.010Test
سنة النشر: 2021
المجموعة: Discovery - University of Dundee Online Publications
الوصف: Developmental venous anomalies (DVAs) are variations in the transmedullary veins required for drainage of the brain. Normally, when occurring in isolation, DVAs are not clinically significant and are therefore usually a benign diagnosis. Thus, they are most often an incidental finding unless associated with an adjacent pathology. However, intracranial haemorrhage induced by a DVA alone can rarely occur and has been scarcely reported. In this case report we discuss a 58-year-old woman who presented with signs and symptoms of a cerebellar syndrome. Following a non-contrast CT, a CT angiogram and MRI contrast scan of the brain, she was found to have a cerebellar DVA and an intracranial haemorrhage. Subsequent imaging 3 months later with CT and MRI redemonstrated additional evidence of a cavernoma. The patient was managed conservatively.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://discovery.dundee.ac.uk/en/publications/a4d0be4f-fc5a-4d55-b375-95e6e7812577Test
DOI: 10.1016/j.radcr.2021.03.010
الإتاحة: https://doi.org/10.1016/j.radcr.2021.03.010Test
https://discovery.dundee.ac.uk/en/publications/a4d0be4f-fc5a-4d55-b375-95e6e7812577Test
https://discovery.dundee.ac.uk/ws/files/73207269/1_s2.0_S1930043321001485_main.pdfTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.64F68994
قاعدة البيانات: BASE