A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I

Abstract Background Neurofibromatosis type 1 is an autosomal dominant genetic disease with characteristic café-au-lait spots, neurofibroma, and dystrophic changes in the bones. However, complications involving atlanto-axial dislocation are rare. Case presentation We report a case of neurofibromatosi...

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Main Authors: Hayato Kinoshita, Naohisa Miyakoshi, Takashi Kobayashi, Toshiki Abe, Kazuma Kikuchi, Yoichi Shimada
Format: Article
Language:English
Published: BMC 2019-04-01
Series:BMC Surgery
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12893-019-0502-z
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spelling doaj-a025d4c60ee04aa18e7b1a9ac700682d2020-11-25T03:23:31ZengBMCBMC Surgery1471-24822019-04-011911610.1186/s12893-019-0502-zA case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type IHayato Kinoshita0Naohisa Miyakoshi1Takashi Kobayashi2Toshiki Abe3Kazuma Kikuchi4Yoichi Shimada5Akita Kosei Medical CenterDepartment of Orthopedic Surgery, Akita University Graduate School of MedicineAkita Kosei Medical CenterAkita Kosei Medical CenterAkita Kosei Medical CenterDepartment of Orthopedic Surgery, Akita University Graduate School of MedicineAbstract Background Neurofibromatosis type 1 is an autosomal dominant genetic disease with characteristic café-au-lait spots, neurofibroma, and dystrophic changes in the bones. However, complications involving atlanto-axial dislocation are rare. Case presentation We report a case of neurofibromatosis with atlanto-axial dislocation. The chief complaints were numbness of the upper limb and gait disturbance. We performed short fusion using the Brooks method. However, recurrence of the dislocation was found after 5 months recovery, and the patient underwent posterior fusion from the occipital bone to C4. Thereafter, she had a good postoperative course. Conclusions Neurofibromatosis patients often exhibit a low bone mineral density because of dystrophic changes, and are prone to fragile bones. In the present case, the use of long fusion at the first surgery may have helped to form a strong fusion of fragile bone.http://link.springer.com/article/10.1186/s12893-019-0502-zCervical spineNeurofibromatosis type 1Long fusion
collection DOAJ
language English
format Article
sources DOAJ
author Hayato Kinoshita
Naohisa Miyakoshi
Takashi Kobayashi
Toshiki Abe
Kazuma Kikuchi
Yoichi Shimada
spellingShingle Hayato Kinoshita
Naohisa Miyakoshi
Takashi Kobayashi
Toshiki Abe
Kazuma Kikuchi
Yoichi Shimada
A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I
BMC Surgery
Cervical spine
Neurofibromatosis type 1
Long fusion
author_facet Hayato Kinoshita
Naohisa Miyakoshi
Takashi Kobayashi
Toshiki Abe
Kazuma Kikuchi
Yoichi Shimada
author_sort Hayato Kinoshita
title A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I
title_short A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I
title_full A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I
title_fullStr A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I
title_full_unstemmed A case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type I
title_sort case report of revision occipital-cervical fusion after atlanto-axial instrumentation failure for neurofibromatosis type i
publisher BMC
series BMC Surgery
issn 1471-2482
publishDate 2019-04-01
description Abstract Background Neurofibromatosis type 1 is an autosomal dominant genetic disease with characteristic café-au-lait spots, neurofibroma, and dystrophic changes in the bones. However, complications involving atlanto-axial dislocation are rare. Case presentation We report a case of neurofibromatosis with atlanto-axial dislocation. The chief complaints were numbness of the upper limb and gait disturbance. We performed short fusion using the Brooks method. However, recurrence of the dislocation was found after 5 months recovery, and the patient underwent posterior fusion from the occipital bone to C4. Thereafter, she had a good postoperative course. Conclusions Neurofibromatosis patients often exhibit a low bone mineral density because of dystrophic changes, and are prone to fragile bones. In the present case, the use of long fusion at the first surgery may have helped to form a strong fusion of fragile bone.
topic Cervical spine
Neurofibromatosis type 1
Long fusion
url http://link.springer.com/article/10.1186/s12893-019-0502-z
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