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Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years

Chordoma is a tumour of notochordal origin which usually involves the sacrum or skull base presenting in adulthood. Chordoma in a mobile spinal segment is infrequent and the authors report an extremely rare presentation of L3 chordoma in a child aged 7 years. Although a benign tumour, mobile segment...

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Detalles Bibliográficos
Autores principales: Killampalli, Vijay V., Power, Dominic, Stirling, Alistair J.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1602195/
https://www.ncbi.nlm.nih.gov/pubmed/16715306
http://dx.doi.org/10.1007/s00586-006-0138-4
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author Killampalli, Vijay V.
Power, Dominic
Stirling, Alistair J.
author_facet Killampalli, Vijay V.
Power, Dominic
Stirling, Alistair J.
author_sort Killampalli, Vijay V.
collection PubMed
description Chordoma is a tumour of notochordal origin which usually involves the sacrum or skull base presenting in adulthood. Chordoma in a mobile spinal segment is infrequent and the authors report an extremely rare presentation of L3 chordoma in a child aged 7 years. Although a benign tumour, mobile segment chordoma is more locally aggressive, more likely to metastasise and has a poorer 5 year survival than sacral and clival lesions. Wide surgical excision and reconstruction is the treatment of choice in vertebral chordoma. This case was treated with staged vertebrectomy and fibular strut graft reconstruction and the results of clinical and radiological follow up at 8 years are presented.
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spelling pubmed-16021952008-08-28 Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years Killampalli, Vijay V. Power, Dominic Stirling, Alistair J. Eur Spine J Case Report Chordoma is a tumour of notochordal origin which usually involves the sacrum or skull base presenting in adulthood. Chordoma in a mobile spinal segment is infrequent and the authors report an extremely rare presentation of L3 chordoma in a child aged 7 years. Although a benign tumour, mobile segment chordoma is more locally aggressive, more likely to metastasise and has a poorer 5 year survival than sacral and clival lesions. Wide surgical excision and reconstruction is the treatment of choice in vertebral chordoma. This case was treated with staged vertebrectomy and fibular strut graft reconstruction and the results of clinical and radiological follow up at 8 years are presented. Springer-Verlag 2006-05-20 2006-10 /pmc/articles/PMC1602195/ /pubmed/16715306 http://dx.doi.org/10.1007/s00586-006-0138-4 Text en © Springer-Verlag 2006
spellingShingle Case Report
Killampalli, Vijay V.
Power, Dominic
Stirling, Alistair J.
Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
title Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
title_full Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
title_fullStr Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
title_full_unstemmed Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
title_short Preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
title_sort preadolescent presentation of a lumbar chordoma: results of vertebrectomy and fibula strut graft reconstruction at 8 years
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1602195/
https://www.ncbi.nlm.nih.gov/pubmed/16715306
http://dx.doi.org/10.1007/s00586-006-0138-4
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AT stirlingalistairj preadolescentpresentationofalumbarchordomaresultsofvertebrectomyandfibulastrutgraftreconstructionat8years