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Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae

We report staged treatment of severe combined spinal deformity in an 11-year-old patient with Ollier disease and abnormal cervical vertebra. Combined scoliosis with systemic pathology and abnormal vertebrae is a rare condition and features atypical deformity location and rapid progression rate and f...

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Autores principales: Ryabykh, S. О., Gubin, A. V., Prudnikova, О. G., Kobyzev, А. Е.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854679/
https://www.ncbi.nlm.nih.gov/pubmed/24436859
http://dx.doi.org/10.1055/s-0032-1329891
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author Ryabykh, S. О.
Gubin, A. V.
Prudnikova, О. G.
Kobyzev, А. Е.
author_facet Ryabykh, S. О.
Gubin, A. V.
Prudnikova, О. G.
Kobyzev, А. Е.
author_sort Ryabykh, S. О.
collection PubMed
description We report staged treatment of severe combined spinal deformity in an 11-year-old patient with Ollier disease and abnormal cervical vertebra. Combined scoliosis with systemic pathology and abnormal vertebrae is a rare condition and features atypical deformity location and rapid progression rate and frequently involves the rib cage and pelvis, disturbing the function of chest organs and skeleton. Progressive deformity resulted in cachexia and acute respiratory failure. A halo-pelvic distraction device assembled of Ilizarov components was employed for a staged surgical treatment performed for lifesaving indications. After vital functions stabilized, the scoliosis curve of the cervical spine was corrected and fixed with a hybrid system of transpedicular supporting points, connecting rods, and connectors that provided staged distraction during growth. The treatment showed good functional and cosmetic result.
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spelling pubmed-38546792014-06-01 Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae Ryabykh, S. О. Gubin, A. V. Prudnikova, О. G. Kobyzev, А. Е. Global Spine J Article We report staged treatment of severe combined spinal deformity in an 11-year-old patient with Ollier disease and abnormal cervical vertebra. Combined scoliosis with systemic pathology and abnormal vertebrae is a rare condition and features atypical deformity location and rapid progression rate and frequently involves the rib cage and pelvis, disturbing the function of chest organs and skeleton. Progressive deformity resulted in cachexia and acute respiratory failure. A halo-pelvic distraction device assembled of Ilizarov components was employed for a staged surgical treatment performed for lifesaving indications. After vital functions stabilized, the scoliosis curve of the cervical spine was corrected and fixed with a hybrid system of transpedicular supporting points, connecting rods, and connectors that provided staged distraction during growth. The treatment showed good functional and cosmetic result. Georg Thieme Verlag KG 2012-11-28 2013-06 /pmc/articles/PMC3854679/ /pubmed/24436859 http://dx.doi.org/10.1055/s-0032-1329891 Text en © Thieme Medical Publishers
spellingShingle Article
Ryabykh, S. О.
Gubin, A. V.
Prudnikova, О. G.
Kobyzev, А. Е.
Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae
title Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae
title_full Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae
title_fullStr Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae
title_full_unstemmed Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae
title_short Treatment of Combined Spinal Deformity in Patient with Ollier Disease and Abnormal Vertebrae
title_sort treatment of combined spinal deformity in patient with ollier disease and abnormal vertebrae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854679/
https://www.ncbi.nlm.nih.gov/pubmed/24436859
http://dx.doi.org/10.1055/s-0032-1329891
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