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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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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