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Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report

Hydrocephalus is a pathological buildup of cerebrospinal fluid within the ventricles leading to ventricular enlargement out of proportion to sulci and subarachnoid spaces. Developmental venous anomaly is a common benign and usually asymptomatic congenital cerebrovascular malformation. Hydrocephalus...

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Detalles Bibliográficos
Autores principales: Xian, Zhaoying, Fung, Steve H., Nakawah, Mohammad Obadah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152591/
https://www.ncbi.nlm.nih.gov/pubmed/32300468
http://dx.doi.org/10.1016/j.radcr.2020.02.014
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author Xian, Zhaoying
Fung, Steve H.
Nakawah, Mohammad Obadah
author_facet Xian, Zhaoying
Fung, Steve H.
Nakawah, Mohammad Obadah
author_sort Xian, Zhaoying
collection PubMed
description Hydrocephalus is a pathological buildup of cerebrospinal fluid within the ventricles leading to ventricular enlargement out of proportion to sulci and subarachnoid spaces. Developmental venous anomaly is a common benign and usually asymptomatic congenital cerebrovascular malformation. Hydrocephalus caused by aqueductal developmental venous anomaly is extremely rare. We describe a case of a 47-year-old man who presents with short-term memory impairment who was found to have a developmental venous anomaly draining bilateral medial thalami through a common collector vein that causes aqueductal stenosis and obstructive hydrocephalus.
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spelling pubmed-71525912020-04-16 Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report Xian, Zhaoying Fung, Steve H. Nakawah, Mohammad Obadah Radiol Case Rep Neuroradiology Hydrocephalus is a pathological buildup of cerebrospinal fluid within the ventricles leading to ventricular enlargement out of proportion to sulci and subarachnoid spaces. Developmental venous anomaly is a common benign and usually asymptomatic congenital cerebrovascular malformation. Hydrocephalus caused by aqueductal developmental venous anomaly is extremely rare. We describe a case of a 47-year-old man who presents with short-term memory impairment who was found to have a developmental venous anomaly draining bilateral medial thalami through a common collector vein that causes aqueductal stenosis and obstructive hydrocephalus. Elsevier 2020-04-08 /pmc/articles/PMC7152591/ /pubmed/32300468 http://dx.doi.org/10.1016/j.radcr.2020.02.014 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://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 Neuroradiology
Xian, Zhaoying
Fung, Steve H.
Nakawah, Mohammad Obadah
Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
title Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
title_full Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
title_fullStr Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
title_full_unstemmed Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
title_short Obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
title_sort obstructive hydrocephalus due to aqueductal stenosis from developmental venous anomaly draining bilateral medial thalami: a case report
topic Neuroradiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152591/
https://www.ncbi.nlm.nih.gov/pubmed/32300468
http://dx.doi.org/10.1016/j.radcr.2020.02.014
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