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Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature

BACKGROUND: Chondroblastoma (CB) is an intermediate tumor of cartilage origin. CB involving the sacrum is a very rare pathology. CASE SUMMARY: A 17-year-old male with sacral CB was diagnosed as CB during the first surgery, and 18 mo later, the tumor recurred and a second surgery was performed with t...

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Autores principales: Zheng, Bo-Wen, Niu, Hua-Qing, Wang, Xiao-Bin, Li, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281409/
https://www.ncbi.nlm.nih.gov/pubmed/34307629
http://dx.doi.org/10.12998/wjcc.v9.i20.5709
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author Zheng, Bo-Wen
Niu, Hua-Qing
Wang, Xiao-Bin
Li, Jing
author_facet Zheng, Bo-Wen
Niu, Hua-Qing
Wang, Xiao-Bin
Li, Jing
author_sort Zheng, Bo-Wen
collection PubMed
description BACKGROUND: Chondroblastoma (CB) is an intermediate tumor of cartilage origin. CB involving the sacrum is a very rare pathology. CASE SUMMARY: A 17-year-old male with sacral CB was diagnosed as CB during the first surgery, and 18 mo later, the tumor recurred and a second surgery was performed with the same pathology result of CB. CONCLUSION: We recommend complete removal of the tumor in a timely manner, provided that surgical conditions are met. At the same time, other diseases should be carefully differentiated in terms of imaging or pathological features so as to avoid erroneous diagnostic conclusions.
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spelling pubmed-82814092021-07-22 Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature Zheng, Bo-Wen Niu, Hua-Qing Wang, Xiao-Bin Li, Jing World J Clin Cases Case Report BACKGROUND: Chondroblastoma (CB) is an intermediate tumor of cartilage origin. CB involving the sacrum is a very rare pathology. CASE SUMMARY: A 17-year-old male with sacral CB was diagnosed as CB during the first surgery, and 18 mo later, the tumor recurred and a second surgery was performed with the same pathology result of CB. CONCLUSION: We recommend complete removal of the tumor in a timely manner, provided that surgical conditions are met. At the same time, other diseases should be carefully differentiated in terms of imaging or pathological features so as to avoid erroneous diagnostic conclusions. Baishideng Publishing Group Inc 2021-07-16 2021-07-16 /pmc/articles/PMC8281409/ /pubmed/34307629 http://dx.doi.org/10.12998/wjcc.v9.i20.5709 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Case Report
Zheng, Bo-Wen
Niu, Hua-Qing
Wang, Xiao-Bin
Li, Jing
Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature
title Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature
title_full Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature
title_fullStr Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature
title_full_unstemmed Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature
title_short Sacral chondroblastoma — a rare location, a rare pathology: A case report and review of literature
title_sort sacral chondroblastoma — a rare location, a rare pathology: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281409/
https://www.ncbi.nlm.nih.gov/pubmed/34307629
http://dx.doi.org/10.12998/wjcc.v9.i20.5709
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