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Spinal Exostosis in a Boy with Multiple Hereditary Exostoses

We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal. Spine radiograph showed a cauliflower-like abnormality of multiple exostoses of the posterior...

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Autores principales: Al Kaissi, Ali, Ganger, Rudolf, Klaushofer, Klaus, Grill, Franz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844191/
https://www.ncbi.nlm.nih.gov/pubmed/24324905
http://dx.doi.org/10.1155/2013/758168
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author Al Kaissi, Ali
Ganger, Rudolf
Klaushofer, Klaus
Grill, Franz
author_facet Al Kaissi, Ali
Ganger, Rudolf
Klaushofer, Klaus
Grill, Franz
author_sort Al Kaissi, Ali
collection PubMed
description We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal. Spine radiograph showed a cauliflower-like abnormality of multiple exostoses of the posterior arch (pedicle) of the thoracic vertebrae (T3–5). Reformatted CT scanning revealed the simultaneous development of intra- and extraspinal osteochondromatosis of T3–5. The spinal cord was compressed by the intraspinal exostosis. Our patient was surgically treated for intraspinal exostoses and showed cessation of neurological deficits. We report what might be a rare association of spinal cord compression in a patient with multiple hereditary exostoses.
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spelling pubmed-38441912013-12-09 Spinal Exostosis in a Boy with Multiple Hereditary Exostoses Al Kaissi, Ali Ganger, Rudolf Klaushofer, Klaus Grill, Franz Case Rep Orthop Case Report We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal. Spine radiograph showed a cauliflower-like abnormality of multiple exostoses of the posterior arch (pedicle) of the thoracic vertebrae (T3–5). Reformatted CT scanning revealed the simultaneous development of intra- and extraspinal osteochondromatosis of T3–5. The spinal cord was compressed by the intraspinal exostosis. Our patient was surgically treated for intraspinal exostoses and showed cessation of neurological deficits. We report what might be a rare association of spinal cord compression in a patient with multiple hereditary exostoses. Hindawi Publishing Corporation 2013 2013-11-10 /pmc/articles/PMC3844191/ /pubmed/24324905 http://dx.doi.org/10.1155/2013/758168 Text en Copyright © 2013 Ali Al Kaissi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al Kaissi, Ali
Ganger, Rudolf
Klaushofer, Klaus
Grill, Franz
Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
title Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
title_full Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
title_fullStr Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
title_full_unstemmed Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
title_short Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
title_sort spinal exostosis in a boy with multiple hereditary exostoses
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844191/
https://www.ncbi.nlm.nih.gov/pubmed/24324905
http://dx.doi.org/10.1155/2013/758168
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