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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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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. |
format | Online Article Text |
id | pubmed-8281409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
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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