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C1-2 cyst presenting with syringobulbia: a case report

Extradural atlantoaxial cysts are typically related to C1-2 degeneration. Intradural cysts may cause secondary syringobulbia depending on the size and cerebrospinal fluid flow obstruction. However, medullary syrinxes have not been previously described with extradural cysts. Treatment of symptomatic...

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Autores principales: Yang, Michael J, Arkun, Knarik, Kryzanski, James T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024048/
https://www.ncbi.nlm.nih.gov/pubmed/33854761
http://dx.doi.org/10.1093/jscr/rjab097
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author Yang, Michael J
Arkun, Knarik
Kryzanski, James T
author_facet Yang, Michael J
Arkun, Knarik
Kryzanski, James T
author_sort Yang, Michael J
collection PubMed
description Extradural atlantoaxial cysts are typically related to C1-2 degeneration. Intradural cysts may cause secondary syringobulbia depending on the size and cerebrospinal fluid flow obstruction. However, medullary syrinxes have not been previously described with extradural cysts. Treatment of symptomatic lesions involves surgical resection, often via a far-lateral approach, with consideration of fusion if C1-2 instability is present. We present a case of an extradural C1-2 cyst with intradural extension causing syringobulbia. Effective surgical resection was accomplished via a far-lateral, partial transcondylar approach without fusion. It is important to recognize that cysts of extradural origin may exhibit intradural extension and compress critical neurovascular structures.
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spelling pubmed-80240482021-04-13 C1-2 cyst presenting with syringobulbia: a case report Yang, Michael J Arkun, Knarik Kryzanski, James T J Surg Case Rep Case Report Extradural atlantoaxial cysts are typically related to C1-2 degeneration. Intradural cysts may cause secondary syringobulbia depending on the size and cerebrospinal fluid flow obstruction. However, medullary syrinxes have not been previously described with extradural cysts. Treatment of symptomatic lesions involves surgical resection, often via a far-lateral approach, with consideration of fusion if C1-2 instability is present. We present a case of an extradural C1-2 cyst with intradural extension causing syringobulbia. Effective surgical resection was accomplished via a far-lateral, partial transcondylar approach without fusion. It is important to recognize that cysts of extradural origin may exhibit intradural extension and compress critical neurovascular structures. Oxford University Press 2021-04-06 /pmc/articles/PMC8024048/ /pubmed/33854761 http://dx.doi.org/10.1093/jscr/rjab097 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2021. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yang, Michael J
Arkun, Knarik
Kryzanski, James T
C1-2 cyst presenting with syringobulbia: a case report
title C1-2 cyst presenting with syringobulbia: a case report
title_full C1-2 cyst presenting with syringobulbia: a case report
title_fullStr C1-2 cyst presenting with syringobulbia: a case report
title_full_unstemmed C1-2 cyst presenting with syringobulbia: a case report
title_short C1-2 cyst presenting with syringobulbia: a case report
title_sort c1-2 cyst presenting with syringobulbia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024048/
https://www.ncbi.nlm.nih.gov/pubmed/33854761
http://dx.doi.org/10.1093/jscr/rjab097
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