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

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 associa...

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Autores principales: Marzouk, Omar, Marzouk, Sherief, Liyanage, Sidath H., Grunwald, Iris Q
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066316/
https://www.ncbi.nlm.nih.gov/pubmed/33912265
http://dx.doi.org/10.1016/j.radcr.2021.03.010
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author Marzouk, Omar
Marzouk, Sherief
Liyanage, Sidath H.
Grunwald, Iris Q
author_facet Marzouk, Omar
Marzouk, Sherief
Liyanage, Sidath H.
Grunwald, Iris Q
author_sort Marzouk, Omar
collection PubMed
description 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.
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spelling pubmed-80663162021-04-27 Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence Marzouk, Omar Marzouk, Sherief Liyanage, Sidath H. Grunwald, Iris Q Radiol Case Rep Case Report 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. Elsevier 2021-04-13 /pmc/articles/PMC8066316/ /pubmed/33912265 http://dx.doi.org/10.1016/j.radcr.2021.03.010 Text en © 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Marzouk, Omar
Marzouk, Sherief
Liyanage, Sidath H.
Grunwald, Iris Q
Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
title Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
title_full Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
title_fullStr Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
title_full_unstemmed Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
title_short Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
title_sort cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066316/
https://www.ncbi.nlm.nih.gov/pubmed/33912265
http://dx.doi.org/10.1016/j.radcr.2021.03.010
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