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Multiple primary chordomas of the lung

We here report the case of a 40-year-old man with primary pulmonary chordomas. Although an abnormality had been noted on a chest radiograph at age 26 years, the patient had not undergone further examination at that time because he was asymptomatic. Standard chest radiographs and computed tomography...

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Detalles Bibliográficos
Autores principales: Ohya, Maki, Yoshida, Kazuo, Shimojo, Hisashi, Shiina, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115605/
https://www.ncbi.nlm.nih.gov/pubmed/30175034
http://dx.doi.org/10.1016/j.rmcr.2018.08.012
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author Ohya, Maki
Yoshida, Kazuo
Shimojo, Hisashi
Shiina, Takayuki
author_facet Ohya, Maki
Yoshida, Kazuo
Shimojo, Hisashi
Shiina, Takayuki
author_sort Ohya, Maki
collection PubMed
description We here report the case of a 40-year-old man with primary pulmonary chordomas. Although an abnormality had been noted on a chest radiograph at age 26 years, the patient had not undergone further examination at that time because he was asymptomatic. Standard chest radiographs and computed tomography showed slow-growing, multiple bilateral pulmonary nodules. Two tumors were resected thoracoscopically to obtain a diagnosis. Pathologic examination resulted in a diagnosis of chordomas. Subsequent systemic examination revealed no additional lesions, not even in the axial skeleton. The patient is alive without any new lesions 38 months after surgery. These clinical and pathological findings suggest that our patient has multiple primary chordomas of the lung, which is an extremely rare condition.
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spelling pubmed-61156052018-08-31 Multiple primary chordomas of the lung Ohya, Maki Yoshida, Kazuo Shimojo, Hisashi Shiina, Takayuki Respir Med Case Rep Case Report We here report the case of a 40-year-old man with primary pulmonary chordomas. Although an abnormality had been noted on a chest radiograph at age 26 years, the patient had not undergone further examination at that time because he was asymptomatic. Standard chest radiographs and computed tomography showed slow-growing, multiple bilateral pulmonary nodules. Two tumors were resected thoracoscopically to obtain a diagnosis. Pathologic examination resulted in a diagnosis of chordomas. Subsequent systemic examination revealed no additional lesions, not even in the axial skeleton. The patient is alive without any new lesions 38 months after surgery. These clinical and pathological findings suggest that our patient has multiple primary chordomas of the lung, which is an extremely rare condition. Elsevier 2018-08-21 /pmc/articles/PMC6115605/ /pubmed/30175034 http://dx.doi.org/10.1016/j.rmcr.2018.08.012 Text en © 2018 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
Ohya, Maki
Yoshida, Kazuo
Shimojo, Hisashi
Shiina, Takayuki
Multiple primary chordomas of the lung
title Multiple primary chordomas of the lung
title_full Multiple primary chordomas of the lung
title_fullStr Multiple primary chordomas of the lung
title_full_unstemmed Multiple primary chordomas of the lung
title_short Multiple primary chordomas of the lung
title_sort multiple primary chordomas of the lung
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115605/
https://www.ncbi.nlm.nih.gov/pubmed/30175034
http://dx.doi.org/10.1016/j.rmcr.2018.08.012
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