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Cerebellar hemorrhage in a healthy young adult: a case report

BACKGROUND: Cavernous venous malformation is an uncommon entity that occurs in around 0.5% of the general population. Cerebellar cavernous venous malformation accounts for 1.2–11.8% of intracranial cavernous venous malformation cases. Patients are commonly asymptomatic until a hemorrhage occurs. In...

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Autores principales: Ibrahim, A. H., Mohamad, N., Mohd Yusof Rasid, T. A., Abdullah, M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580125/
https://www.ncbi.nlm.nih.gov/pubmed/36258203
http://dx.doi.org/10.1186/s13256-022-03584-4
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author Ibrahim, A. H.
Mohamad, N.
Mohd Yusof Rasid, T. A.
Abdullah, M. S.
author_facet Ibrahim, A. H.
Mohamad, N.
Mohd Yusof Rasid, T. A.
Abdullah, M. S.
author_sort Ibrahim, A. H.
collection PubMed
description BACKGROUND: Cavernous venous malformation is an uncommon entity that occurs in around 0.5% of the general population. Cerebellar cavernous venous malformation accounts for 1.2–11.8% of intracranial cavernous venous malformation cases. Patients are commonly asymptomatic until a hemorrhage occurs. In approximately 20% of the cases, cavernous venous malformation and developmental venous anomalies occur together, called mixed vascular malformation. Our case report reveals the imaging features of the mixed vascular malformation and highlights the appropriate imaging modality and sequence to detect the abnormalities. CASE PRESENTATION: We report the case of a 15-year-old Malay male, a healthy young male who presented with dizziness, vomiting, and mild headache for 1 month. Computed tomography brain imaging at presentation revealed cerebellar hemorrhage with multiple cavernous venous malformation and coexisting developmental venous anomalies, which was then confirmed by magnetic resonance imaging. The patient was started on dexamethasone 4 mg four times a day, observed in the ward, and discharged well without neurological sequelae. CONCLUSION: A cavernous malformation with concurrent developmental venous anomalies requires accurate diagnosis. Our case report contributes to the literature on the imaging diagnosis of this disease, which is beneficial for current and future reference.
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spelling pubmed-95801252022-10-20 Cerebellar hemorrhage in a healthy young adult: a case report Ibrahim, A. H. Mohamad, N. Mohd Yusof Rasid, T. A. Abdullah, M. S. J Med Case Rep Case Report BACKGROUND: Cavernous venous malformation is an uncommon entity that occurs in around 0.5% of the general population. Cerebellar cavernous venous malformation accounts for 1.2–11.8% of intracranial cavernous venous malformation cases. Patients are commonly asymptomatic until a hemorrhage occurs. In approximately 20% of the cases, cavernous venous malformation and developmental venous anomalies occur together, called mixed vascular malformation. Our case report reveals the imaging features of the mixed vascular malformation and highlights the appropriate imaging modality and sequence to detect the abnormalities. CASE PRESENTATION: We report the case of a 15-year-old Malay male, a healthy young male who presented with dizziness, vomiting, and mild headache for 1 month. Computed tomography brain imaging at presentation revealed cerebellar hemorrhage with multiple cavernous venous malformation and coexisting developmental venous anomalies, which was then confirmed by magnetic resonance imaging. The patient was started on dexamethasone 4 mg four times a day, observed in the ward, and discharged well without neurological sequelae. CONCLUSION: A cavernous malformation with concurrent developmental venous anomalies requires accurate diagnosis. Our case report contributes to the literature on the imaging diagnosis of this disease, which is beneficial for current and future reference. BioMed Central 2022-10-19 /pmc/articles/PMC9580125/ /pubmed/36258203 http://dx.doi.org/10.1186/s13256-022-03584-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Ibrahim, A. H.
Mohamad, N.
Mohd Yusof Rasid, T. A.
Abdullah, M. S.
Cerebellar hemorrhage in a healthy young adult: a case report
title Cerebellar hemorrhage in a healthy young adult: a case report
title_full Cerebellar hemorrhage in a healthy young adult: a case report
title_fullStr Cerebellar hemorrhage in a healthy young adult: a case report
title_full_unstemmed Cerebellar hemorrhage in a healthy young adult: a case report
title_short Cerebellar hemorrhage in a healthy young adult: a case report
title_sort cerebellar hemorrhage in a healthy young adult: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580125/
https://www.ncbi.nlm.nih.gov/pubmed/36258203
http://dx.doi.org/10.1186/s13256-022-03584-4
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