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Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch

AVMs are congenital lesions that predispose patients to intracranial hemorrhage and resultant neurological deficits. These deficits are often focal and due to the presence of local neurologic disruption from hemorrhage in the contralateral cerebral hemisphere. We present a rare case of a patient wit...

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Autores principales: Dibble, Christopher F., Wemhoff, Michael P., Ibrahim, Tarik, Sasaki-Adams, Deanna, Solander, Sten, Germanwala, Anand V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426657/
https://www.ncbi.nlm.nih.gov/pubmed/26000183
http://dx.doi.org/10.1155/2015/921930
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author Dibble, Christopher F.
Wemhoff, Michael P.
Ibrahim, Tarik
Sasaki-Adams, Deanna
Solander, Sten
Germanwala, Anand V.
author_facet Dibble, Christopher F.
Wemhoff, Michael P.
Ibrahim, Tarik
Sasaki-Adams, Deanna
Solander, Sten
Germanwala, Anand V.
author_sort Dibble, Christopher F.
collection PubMed
description AVMs are congenital lesions that predispose patients to intracranial hemorrhage and resultant neurological deficits. These deficits are often focal and due to the presence of local neurologic disruption from hemorrhage in the contralateral cerebral hemisphere. We present a rare case of a patient with ipsilateral neurological deficits due to Kernohan's Notch phenomenon resulting from hemorrhage from an AVM. A 31-year-old woman with seizures underwent MR and angiographic imaging which confirmed an unruptured left parietal AVM. The patient declined treatment and presented with obtundation 4 years later. Imaging revealed an acute left parietal ICH and SDH with significant mass effect. The patient underwent emergent hemicraniectomy and hematoma evacuation. Postoperatively, she made significant improvement and was following commands contralaterally with ipsilateral hemiplegia. MR imaging revealed right Kernohan's Notch. The patient had significant rehabilitation with neurological improvement. She eventually underwent elective embolization followed by subsequent surgical resection and bone replacement. Three years from the initial hemorrhage, the patient had only mild left-sided weakness and ambulates without assistance. A false localizing sign, Kernohan's Notch phenomenon, should be considered in the setting of AVM hemorrhage with paradoxical motor impairment and can be identified through MRI.
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spelling pubmed-44266572015-05-21 Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch Dibble, Christopher F. Wemhoff, Michael P. Ibrahim, Tarik Sasaki-Adams, Deanna Solander, Sten Germanwala, Anand V. Case Rep Neurol Med Case Report AVMs are congenital lesions that predispose patients to intracranial hemorrhage and resultant neurological deficits. These deficits are often focal and due to the presence of local neurologic disruption from hemorrhage in the contralateral cerebral hemisphere. We present a rare case of a patient with ipsilateral neurological deficits due to Kernohan's Notch phenomenon resulting from hemorrhage from an AVM. A 31-year-old woman with seizures underwent MR and angiographic imaging which confirmed an unruptured left parietal AVM. The patient declined treatment and presented with obtundation 4 years later. Imaging revealed an acute left parietal ICH and SDH with significant mass effect. The patient underwent emergent hemicraniectomy and hematoma evacuation. Postoperatively, she made significant improvement and was following commands contralaterally with ipsilateral hemiplegia. MR imaging revealed right Kernohan's Notch. The patient had significant rehabilitation with neurological improvement. She eventually underwent elective embolization followed by subsequent surgical resection and bone replacement. Three years from the initial hemorrhage, the patient had only mild left-sided weakness and ambulates without assistance. A false localizing sign, Kernohan's Notch phenomenon, should be considered in the setting of AVM hemorrhage with paradoxical motor impairment and can be identified through MRI. Hindawi Publishing Corporation 2015 2015-04-27 /pmc/articles/PMC4426657/ /pubmed/26000183 http://dx.doi.org/10.1155/2015/921930 Text en Copyright © 2015 Christopher F. Dibble et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Dibble, Christopher F.
Wemhoff, Michael P.
Ibrahim, Tarik
Sasaki-Adams, Deanna
Solander, Sten
Germanwala, Anand V.
Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch
title Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch
title_full Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch
title_fullStr Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch
title_full_unstemmed Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch
title_short Ruptured Arteriovenous Malformation Presenting with Kernohan's Notch
title_sort ruptured arteriovenous malformation presenting with kernohan's notch
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426657/
https://www.ncbi.nlm.nih.gov/pubmed/26000183
http://dx.doi.org/10.1155/2015/921930
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