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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...

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Autores principales: Ono, Yuichi, Hongo, Michio, Kasukawa, Yuji, Misawa, Akiko, Kudo, Daisuke, Miyakoshi, Naohisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
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.
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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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