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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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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. |
format | Online Article Text |
id | pubmed-4678783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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