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Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report

Developmental venous anomalies (DVAs) are composed of mature venous vessels that lack malformed or neoplastic elements. Although the hemorrhage risk is considered negligible, some patients may have neurological symptoms attributable to acute infarction or intracranial hemorrhage secondary to thrombo...

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Autores principales: Barrenechea, Ignacio J., Márquez, Luis M., Cortadi, Vanina A., Rojas, Héctor P, Ingledew, Robin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Cerebrovascular Surgeons and Korean NeuroEndovascular Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555621/
https://www.ncbi.nlm.nih.gov/pubmed/36623888
http://dx.doi.org/10.7461/jcen.2023.E2022.03.004
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author Barrenechea, Ignacio J.
Márquez, Luis M.
Cortadi, Vanina A.
Rojas, Héctor P
Ingledew, Robin
author_facet Barrenechea, Ignacio J.
Márquez, Luis M.
Cortadi, Vanina A.
Rojas, Héctor P
Ingledew, Robin
author_sort Barrenechea, Ignacio J.
collection PubMed
description Developmental venous anomalies (DVAs) are composed of mature venous vessels that lack malformed or neoplastic elements. Although the hemorrhage risk is considered negligible, some patients may have neurological symptoms attributable to acute infarction or intracranial hemorrhage secondary to thrombosis, in the absence of a coexisting cavernous malformation. We report the case of a 42-year-old patient who presented with acute left-hand paresis secondary to a subcortical hemorrhage. This bleeding originated from a DVA in the corticospinal tract area and was surgically drained through an awake craniotomy. To accomplish this, we used a trans-precentral sulcus approach. After the complete removal of the coagulum, small venous channels appeared, which were coagulated. No associated cavernoma was found. Although the main DVA trunk was left patent, no signs of ischemia or venous infarction were observed after coagulating the small venous channels found inside the hematoma cavity. Two weeks after the procedure, the patient’s hand function improved, and he was able to resume desktop work. DVA-associated hemorrhage within the cortico-spinal tract could be safely removed with modern awake mapping techniques. This technique allowed the patient to rapidly improve his hand function.
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spelling pubmed-105556212023-10-07 Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report Barrenechea, Ignacio J. Márquez, Luis M. Cortadi, Vanina A. Rojas, Héctor P Ingledew, Robin J Cerebrovasc Endovasc Neurosurg Case Report Developmental venous anomalies (DVAs) are composed of mature venous vessels that lack malformed or neoplastic elements. Although the hemorrhage risk is considered negligible, some patients may have neurological symptoms attributable to acute infarction or intracranial hemorrhage secondary to thrombosis, in the absence of a coexisting cavernous malformation. We report the case of a 42-year-old patient who presented with acute left-hand paresis secondary to a subcortical hemorrhage. This bleeding originated from a DVA in the corticospinal tract area and was surgically drained through an awake craniotomy. To accomplish this, we used a trans-precentral sulcus approach. After the complete removal of the coagulum, small venous channels appeared, which were coagulated. No associated cavernoma was found. Although the main DVA trunk was left patent, no signs of ischemia or venous infarction were observed after coagulating the small venous channels found inside the hematoma cavity. Two weeks after the procedure, the patient’s hand function improved, and he was able to resume desktop work. DVA-associated hemorrhage within the cortico-spinal tract could be safely removed with modern awake mapping techniques. This technique allowed the patient to rapidly improve his hand function. Korean Society of Cerebrovascular Surgeons and Korean NeuroEndovascular Society 2023-09 2023-01-10 /pmc/articles/PMC10555621/ /pubmed/36623888 http://dx.doi.org/10.7461/jcen.2023.E2022.03.004 Text en Copyright © 2023 by KSCVS and KoNES https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Barrenechea, Ignacio J.
Márquez, Luis M.
Cortadi, Vanina A.
Rojas, Héctor P
Ingledew, Robin
Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report
title Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report
title_full Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report
title_fullStr Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report
title_full_unstemmed Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report
title_short Awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: A case report
title_sort awake craniotomy removal of a corticospinal tract developmental venous anomaly hemorrhage: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555621/
https://www.ncbi.nlm.nih.gov/pubmed/36623888
http://dx.doi.org/10.7461/jcen.2023.E2022.03.004
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