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A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation

Eight syndrome is defined as the combination of a unilateral conjugate gaze palsy and ipsilateral seventh cranial nerve palsy. It may occur as a result of demyelinating, vascular, infectious, or compressive lesions of the brainstem localized to the caudal pontine tegmentum. A 43-year-old woman was a...

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Autores principales: Top Kartı, Dilek, Kıyat, Pelin, Kartı, Ömer, Çelebisoy, Neşe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286839/
https://www.ncbi.nlm.nih.gov/pubmed/37345329
http://dx.doi.org/10.4274/tjo.galenos.2023.19054
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author Top Kartı, Dilek
Kıyat, Pelin
Kartı, Ömer
Çelebisoy, Neşe
author_facet Top Kartı, Dilek
Kıyat, Pelin
Kartı, Ömer
Çelebisoy, Neşe
author_sort Top Kartı, Dilek
collection PubMed
description Eight syndrome is defined as the combination of a unilateral conjugate gaze palsy and ipsilateral seventh cranial nerve palsy. It may occur as a result of demyelinating, vascular, infectious, or compressive lesions of the brainstem localized to the caudal pontine tegmentum. A 43-year-old woman was admitted to our clinic with complaints of headache, inability to look to the left, and weakness on the left side of her face. The complaints had begun abruptly about a month before her admission. Suboccipital decompression surgery for type I Chiari malformation had been performed 10 years earlier. Neuro-ophthalmological examination revealed left-sided horizontal gaze palsy and anisocoria. Cranial and cervical magnetic resonance images revealed cerebellar tonsillar herniation and syringomyelia, the latter of which was considered to be the cause of eight syndrome. No interventions were performed, and periodic follow-up was advised on neurosurgical consultation. Left gaze palsy and facial palsy recovered almost completely in three months, while the anisocoria persisted. Syringomyelia should be considered among the causes of horizontal gaze palsy plus ipsilateral seventh nerve palsy, termed as eight syndrome. Clinical suspicion and appropriate radiological examination can aid in the diagnosis.
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spelling pubmed-102868392023-06-23 A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation Top Kartı, Dilek Kıyat, Pelin Kartı, Ömer Çelebisoy, Neşe Turk J Ophthalmol Case Report Eight syndrome is defined as the combination of a unilateral conjugate gaze palsy and ipsilateral seventh cranial nerve palsy. It may occur as a result of demyelinating, vascular, infectious, or compressive lesions of the brainstem localized to the caudal pontine tegmentum. A 43-year-old woman was admitted to our clinic with complaints of headache, inability to look to the left, and weakness on the left side of her face. The complaints had begun abruptly about a month before her admission. Suboccipital decompression surgery for type I Chiari malformation had been performed 10 years earlier. Neuro-ophthalmological examination revealed left-sided horizontal gaze palsy and anisocoria. Cranial and cervical magnetic resonance images revealed cerebellar tonsillar herniation and syringomyelia, the latter of which was considered to be the cause of eight syndrome. No interventions were performed, and periodic follow-up was advised on neurosurgical consultation. Left gaze palsy and facial palsy recovered almost completely in three months, while the anisocoria persisted. Syringomyelia should be considered among the causes of horizontal gaze palsy plus ipsilateral seventh nerve palsy, termed as eight syndrome. Clinical suspicion and appropriate radiological examination can aid in the diagnosis. Galenos Publishing 2023-06 2023-06-21 /pmc/articles/PMC10286839/ /pubmed/37345329 http://dx.doi.org/10.4274/tjo.galenos.2023.19054 Text en © Copyright 2023 by Turkish Ophthalmological Association | Turkish Journal of Ophthalmology, published by Galenos Publishing House. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of 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
Top Kartı, Dilek
Kıyat, Pelin
Kartı, Ömer
Çelebisoy, Neşe
A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation
title A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation
title_full A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation
title_fullStr A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation
title_full_unstemmed A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation
title_short A Rare Case Report of Eight Syndrome Secondary to Syringomyelia Associated with Type I Chiari Malformation
title_sort rare case report of eight syndrome secondary to syringomyelia associated with type i chiari malformation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286839/
https://www.ncbi.nlm.nih.gov/pubmed/37345329
http://dx.doi.org/10.4274/tjo.galenos.2023.19054
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