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A giant lumbar chordoma: A case report

RATIONALE: Chordomas are malignant neoplasms derived from incomplete regression of notochordal tissue along the craniococcygeal axis.It is rare for Chordoma arising from the lumbar spine and the traditional long-term prognosis is typically poor. PATIENT CONCERNS: The persistent pain in the left side...

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Autores principales: Zhou, Yibiao, Hu, Bolin, Wu, Zhiwei, Cheng, Hanxiong, Dai, Min, Zhang, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023704/
https://www.ncbi.nlm.nih.gov/pubmed/29924012
http://dx.doi.org/10.1097/MD.0000000000011128
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author Zhou, Yibiao
Hu, Bolin
Wu, Zhiwei
Cheng, Hanxiong
Dai, Min
Zhang, Bin
author_facet Zhou, Yibiao
Hu, Bolin
Wu, Zhiwei
Cheng, Hanxiong
Dai, Min
Zhang, Bin
author_sort Zhou, Yibiao
collection PubMed
description RATIONALE: Chordomas are malignant neoplasms derived from incomplete regression of notochordal tissue along the craniococcygeal axis.It is rare for Chordoma arising from the lumbar spine and the traditional long-term prognosis is typically poor. PATIENT CONCERNS: The persistent pain in the left side of the waist about 2 years. DIAGNOSES: Chordoma. INTERVENTIONS: The patient was treated with surgical resection of the total tumor, followed by the spinal internal fixation of L1 to L2 with pedicle screws. OUTCOMES: After 5 month follow-up,we find the recurrence in the original lesion.At the 15 month follow-up,the patient was dead after a lot of times revisit by various doctor. LESSONS: So It is suggest that the diagnosis should be carried out accurately at the early stage, the lesions and source of lesions should be cut away as broadly as possible, also the radiation and chemotherapy should be carried out after the operation as necessary.
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spelling pubmed-60237042018-07-03 A giant lumbar chordoma: A case report Zhou, Yibiao Hu, Bolin Wu, Zhiwei Cheng, Hanxiong Dai, Min Zhang, Bin Medicine (Baltimore) Research Article RATIONALE: Chordomas are malignant neoplasms derived from incomplete regression of notochordal tissue along the craniococcygeal axis.It is rare for Chordoma arising from the lumbar spine and the traditional long-term prognosis is typically poor. PATIENT CONCERNS: The persistent pain in the left side of the waist about 2 years. DIAGNOSES: Chordoma. INTERVENTIONS: The patient was treated with surgical resection of the total tumor, followed by the spinal internal fixation of L1 to L2 with pedicle screws. OUTCOMES: After 5 month follow-up,we find the recurrence in the original lesion.At the 15 month follow-up,the patient was dead after a lot of times revisit by various doctor. LESSONS: So It is suggest that the diagnosis should be carried out accurately at the early stage, the lesions and source of lesions should be cut away as broadly as possible, also the radiation and chemotherapy should be carried out after the operation as necessary. Wolters Kluwer Health 2018-06-22 /pmc/articles/PMC6023704/ /pubmed/29924012 http://dx.doi.org/10.1097/MD.0000000000011128 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Zhou, Yibiao
Hu, Bolin
Wu, Zhiwei
Cheng, Hanxiong
Dai, Min
Zhang, Bin
A giant lumbar chordoma: A case report
title A giant lumbar chordoma: A case report
title_full A giant lumbar chordoma: A case report
title_fullStr A giant lumbar chordoma: A case report
title_full_unstemmed A giant lumbar chordoma: A case report
title_short A giant lumbar chordoma: A case report
title_sort giant lumbar chordoma: a case report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023704/
https://www.ncbi.nlm.nih.gov/pubmed/29924012
http://dx.doi.org/10.1097/MD.0000000000011128
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