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The chordoma arised from ilium: A rare case report

Chordomas are malignant tumors that originate in embryonic notochordal remnants. The sacrum and skull are the most common sites; the mobile spine and other bones are extremely rare sites. We describe a 45-year-old man who presented with a lytic lesion in his left ilium. Imaging and pathology of a bi...

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Detalles Bibliográficos
Autores principales: Yang, Yongkun, Niu, Xiaohui, Li, Lan, Ding, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678783/
https://www.ncbi.nlm.nih.gov/pubmed/26730357
http://dx.doi.org/10.1016/j.jbo.2015.09.004
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author Yang, Yongkun
Niu, Xiaohui
Li, Lan
Ding, Yi
author_facet Yang, Yongkun
Niu, Xiaohui
Li, Lan
Ding, Yi
author_sort Yang, Yongkun
collection PubMed
description Chordomas are malignant tumors that originate in embryonic notochordal remnants. The sacrum and skull are the most common sites; the mobile spine and other bones are extremely rare sites. We describe a 45-year-old man who presented with a lytic lesion in his left ilium. Imaging and pathology of a biopsy specimen suggested a malignant bone tumor; wide resection was accordingly performed. The morphology and immunohistochemistry of the operative specimen showed obvious characteristics of classic chordoma. To our knowledge, this is the first reported case of a chordoma originating in the ilium. Chordoma should therefore be considered in the differential diagnosis of lytic lesions in the ilium.
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spelling pubmed-46787832016-01-04 The chordoma arised from ilium: A rare case report Yang, Yongkun Niu, Xiaohui Li, Lan Ding, Yi J Bone Oncol Case Report Chordomas are malignant tumors that originate in embryonic notochordal remnants. The sacrum and skull are the most common sites; the mobile spine and other bones are extremely rare sites. We describe a 45-year-old man who presented with a lytic lesion in his left ilium. Imaging and pathology of a biopsy specimen suggested a malignant bone tumor; wide resection was accordingly performed. The morphology and immunohistochemistry of the operative specimen showed obvious characteristics of classic chordoma. To our knowledge, this is the first reported case of a chordoma originating in the ilium. Chordoma should therefore be considered in the differential diagnosis of lytic lesions in the ilium. Elsevier 2015-10-01 /pmc/articles/PMC4678783/ /pubmed/26730357 http://dx.doi.org/10.1016/j.jbo.2015.09.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yang, Yongkun
Niu, Xiaohui
Li, Lan
Ding, Yi
The chordoma arised from ilium: A rare case report
title The chordoma arised from ilium: A rare case report
title_full The chordoma arised from ilium: A rare case report
title_fullStr The chordoma arised from ilium: A rare case report
title_full_unstemmed The chordoma arised from ilium: A rare case report
title_short The chordoma arised from ilium: A rare case report
title_sort chordoma arised from ilium: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678783/
https://www.ncbi.nlm.nih.gov/pubmed/26730357
http://dx.doi.org/10.1016/j.jbo.2015.09.004
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