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Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report
BACKGROUND: Atlantoaxial rotatory fixation (AARF) can be caused by infection, rheumatoid arthritis, surgery of head and neck, and congenital diseases. Type 1 neurofibromatosis (NF-1) is often associated with various musculoskeletal diseases, but few reports have described AARF with NF-1. Here, we re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888303/ https://www.ncbi.nlm.nih.gov/pubmed/35242406 http://dx.doi.org/10.25259/SNI_1171_2021 |
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author | Ono, Yuichi Hongo, Michio Kasukawa, Yuji Misawa, Akiko Kudo, Daisuke Miyakoshi, Naohisa |
author_facet | Ono, Yuichi Hongo, Michio Kasukawa, Yuji Misawa, Akiko Kudo, Daisuke Miyakoshi, Naohisa |
author_sort | Ono, Yuichi |
collection | PubMed |
description | BACKGROUND: Atlantoaxial rotatory fixation (AARF) can be caused by infection, rheumatoid arthritis, surgery of head and neck, and congenital diseases. Type 1 neurofibromatosis (NF-1) is often associated with various musculoskeletal diseases, but few reports have described AARF with NF-1. Here, we report the success of a closed reduction and halo fixation utilized to treat chronic AARF with NF-1 in a 7-year-old female. CASE DESCRIPTION: A 7-year-old female with NF-1 presented with a 2-month history of torticollis and neck pain. C2 facet deformity had previously been identified on computed tomography (CT) before the onset of neck pain. Cervical radiography and CT showed AARF classified Fielding’s Type I and Ishii’s Grade II. Following 2 weeks of cervical traction, a closed reduction was followed by halo fixation that was utilized for 2 months. The patient fully recovered cervical range of motion following halo vest removal 4 months later. Further, the follow-up CT documented a normal atlantoaxial joint despite residual C2 facet deformity. In addition, no recurrence was evident 2 years later. CONCLUSION: Halo fixation for chronic AARF with NF-1 proved effective. C2 facet deformity associated with NF-1 might have contributed to the onset of AARF. |
format | Online Article Text |
id | pubmed-8888303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-88883032022-03-02 Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report Ono, Yuichi Hongo, Michio Kasukawa, Yuji Misawa, Akiko Kudo, Daisuke Miyakoshi, Naohisa Surg Neurol Int Case Report BACKGROUND: Atlantoaxial rotatory fixation (AARF) can be caused by infection, rheumatoid arthritis, surgery of head and neck, and congenital diseases. Type 1 neurofibromatosis (NF-1) is often associated with various musculoskeletal diseases, but few reports have described AARF with NF-1. Here, we report the success of a closed reduction and halo fixation utilized to treat chronic AARF with NF-1 in a 7-year-old female. CASE DESCRIPTION: A 7-year-old female with NF-1 presented with a 2-month history of torticollis and neck pain. C2 facet deformity had previously been identified on computed tomography (CT) before the onset of neck pain. Cervical radiography and CT showed AARF classified Fielding’s Type I and Ishii’s Grade II. Following 2 weeks of cervical traction, a closed reduction was followed by halo fixation that was utilized for 2 months. The patient fully recovered cervical range of motion following halo vest removal 4 months later. Further, the follow-up CT documented a normal atlantoaxial joint despite residual C2 facet deformity. In addition, no recurrence was evident 2 years later. CONCLUSION: Halo fixation for chronic AARF with NF-1 proved effective. C2 facet deformity associated with NF-1 might have contributed to the onset of AARF. Scientific Scholar 2022-02-11 /pmc/articles/PMC8888303/ /pubmed/35242406 http://dx.doi.org/10.25259/SNI_1171_2021 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Ono, Yuichi Hongo, Michio Kasukawa, Yuji Misawa, Akiko Kudo, Daisuke Miyakoshi, Naohisa Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report |
title | Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report |
title_full | Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report |
title_fullStr | Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report |
title_full_unstemmed | Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report |
title_short | Chronic atlantoaxial rotatory fixation with neurofibromatosis type I: A case report |
title_sort | chronic atlantoaxial rotatory fixation with neurofibromatosis type i: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888303/ https://www.ncbi.nlm.nih.gov/pubmed/35242406 http://dx.doi.org/10.25259/SNI_1171_2021 |
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