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Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report
Complex Chiari malformation (CCM) is a spectrum of congenital bony and soft tissue abnormalities, which includes Chiari 1.5 malformation, medullary kinking, retroflexed odontoid, abnormal clival-cervical angle (CXA), occipitalization of the atlas, basilar invagination, syringomyelia, and scoliosis....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057885/ https://www.ncbi.nlm.nih.gov/pubmed/32181187 http://dx.doi.org/10.4103/ajns.AJNS_344_19 |
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author | Balasubramanian, Sneha Chitra Saphiya, Navas Nazumudeen Madan, Abu Mathews, Shobha Sara Nair, Ajith Rajappan |
author_facet | Balasubramanian, Sneha Chitra Saphiya, Navas Nazumudeen Madan, Abu Mathews, Shobha Sara Nair, Ajith Rajappan |
author_sort | Balasubramanian, Sneha Chitra |
collection | PubMed |
description | Complex Chiari malformation (CCM) is a spectrum of congenital bony and soft tissue abnormalities, which includes Chiari 1.5 malformation, medullary kinking, retroflexed odontoid, abnormal clival-cervical angle (CXA), occipitalization of the atlas, basilar invagination, syringomyelia, and scoliosis. CCM usually manifests in the pediatric age group and is a challenging entity to treat. It requires detailed evaluation of craniometric indices to decide the appropriate surgical management. Patients with maximum perpendicular distance of dens to the line from the basion to the inferoposterior part of the C2 body (pBC2 line) of more than 9 mm and CXA <125° require a posterior fixation and will benefit from a single-stage posterior fusion and foramen magnum decompression (FMD). We report a rare case of CCM manifesting in a 32-year-old male with brainstem compression and bulbar symptoms. We could realign the craniovertebral junction with only a C1-C2 fixation by a modified distraction, compression, extension, and reduction technique and also relieve the neural compression by FMD and tonsillar resection in a single surgery with a good outcome. The authors find it to be an effective alternative to avoid the occipital fixation. |
format | Online Article Text |
id | pubmed-7057885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-70578852020-03-16 Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report Balasubramanian, Sneha Chitra Saphiya, Navas Nazumudeen Madan, Abu Mathews, Shobha Sara Nair, Ajith Rajappan Asian J Neurosurg Case Report Complex Chiari malformation (CCM) is a spectrum of congenital bony and soft tissue abnormalities, which includes Chiari 1.5 malformation, medullary kinking, retroflexed odontoid, abnormal clival-cervical angle (CXA), occipitalization of the atlas, basilar invagination, syringomyelia, and scoliosis. CCM usually manifests in the pediatric age group and is a challenging entity to treat. It requires detailed evaluation of craniometric indices to decide the appropriate surgical management. Patients with maximum perpendicular distance of dens to the line from the basion to the inferoposterior part of the C2 body (pBC2 line) of more than 9 mm and CXA <125° require a posterior fixation and will benefit from a single-stage posterior fusion and foramen magnum decompression (FMD). We report a rare case of CCM manifesting in a 32-year-old male with brainstem compression and bulbar symptoms. We could realign the craniovertebral junction with only a C1-C2 fixation by a modified distraction, compression, extension, and reduction technique and also relieve the neural compression by FMD and tonsillar resection in a single surgery with a good outcome. The authors find it to be an effective alternative to avoid the occipital fixation. Wolters Kluwer - Medknow 2020-02-25 /pmc/articles/PMC7057885/ /pubmed/32181187 http://dx.doi.org/10.4103/ajns.AJNS_344_19 Text en Copyright: © 2020 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Balasubramanian, Sneha Chitra Saphiya, Navas Nazumudeen Madan, Abu Mathews, Shobha Sara Nair, Ajith Rajappan Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report |
title | Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report |
title_full | Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report |
title_fullStr | Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report |
title_full_unstemmed | Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report |
title_short | Complex Chiari Malformation Presenting with Bulbar Symptoms in an Adult: Single-stage Posterior Fusion and Foramen Magnum Decompression: A Rare Case Report |
title_sort | complex chiari malformation presenting with bulbar symptoms in an adult: single-stage posterior fusion and foramen magnum decompression: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057885/ https://www.ncbi.nlm.nih.gov/pubmed/32181187 http://dx.doi.org/10.4103/ajns.AJNS_344_19 |
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