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Chondrosarcoma of the toe: A case report and literature review
BACKGROUND: Chondrosarcoma of the foot is a rare malignant bone tumour, and it is even rarer when it originates in a toe bone. Surgical excision is the only effective treatment. The osteolytic destruction of the tumour severely affects limb function and carries the risk of distant metastasis. Most s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477028/ https://www.ncbi.nlm.nih.gov/pubmed/36157642 http://dx.doi.org/10.12998/wjcc.v10.i25.9132 |
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author | Zhou, Li-Bo Zhang, He-Cheng Dong, Zai-Gang Wang, Chao-Chao |
author_facet | Zhou, Li-Bo Zhang, He-Cheng Dong, Zai-Gang Wang, Chao-Chao |
author_sort | Zhou, Li-Bo |
collection | PubMed |
description | BACKGROUND: Chondrosarcoma of the foot is a rare malignant bone tumour, and it is even rarer when it originates in a toe bone. Surgical excision is the only effective treatment. The osteolytic destruction of the tumour severely affects limb function and carries the risk of distant metastasis. Most such tumours are removed surgically to minimize local recurrence and distant metastases, maximize limb function, and prolong the patient's tumour-free survival time. The main objective of this article is to present the case of a chondrosarcoma that invaded the first phalanx of the left foot and formed a large phalangeal mass with osteolytic destruction of the distal bone. CASE SUMMARY: A 74-year-old man suffered from swelling of his left toe for six months, with pain and swelling for two months. Computed tomography and magnetic resonance imaging showed that the tumour on the first phalanx of the left foot was approximately 54.9 mm × 44.6 mm, surrounded by a significant soft tissue signal mass, with osteolytic destruction of the distal phalanx and a speckled bone-like high-density shadow within it. CONCLUSION: Chondrosarcoma occurring in a toe bone is extremely rare. In this case, extensive surgical resection of the large low-grade chondrosarcoma, which showed osteolytic destruction and invaded the distal metatarsal bone, was safe and effective. |
format | Online Article Text |
id | pubmed-9477028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-94770282022-09-23 Chondrosarcoma of the toe: A case report and literature review Zhou, Li-Bo Zhang, He-Cheng Dong, Zai-Gang Wang, Chao-Chao World J Clin Cases Case Report BACKGROUND: Chondrosarcoma of the foot is a rare malignant bone tumour, and it is even rarer when it originates in a toe bone. Surgical excision is the only effective treatment. The osteolytic destruction of the tumour severely affects limb function and carries the risk of distant metastasis. Most such tumours are removed surgically to minimize local recurrence and distant metastases, maximize limb function, and prolong the patient's tumour-free survival time. The main objective of this article is to present the case of a chondrosarcoma that invaded the first phalanx of the left foot and formed a large phalangeal mass with osteolytic destruction of the distal bone. CASE SUMMARY: A 74-year-old man suffered from swelling of his left toe for six months, with pain and swelling for two months. Computed tomography and magnetic resonance imaging showed that the tumour on the first phalanx of the left foot was approximately 54.9 mm × 44.6 mm, surrounded by a significant soft tissue signal mass, with osteolytic destruction of the distal phalanx and a speckled bone-like high-density shadow within it. CONCLUSION: Chondrosarcoma occurring in a toe bone is extremely rare. In this case, extensive surgical resection of the large low-grade chondrosarcoma, which showed osteolytic destruction and invaded the distal metatarsal bone, was safe and effective. Baishideng Publishing Group Inc 2022-09-06 2022-09-06 /pmc/articles/PMC9477028/ /pubmed/36157642 http://dx.doi.org/10.12998/wjcc.v10.i25.9132 Text en ©The Author(s) 2022. 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. |
spellingShingle | Case Report Zhou, Li-Bo Zhang, He-Cheng Dong, Zai-Gang Wang, Chao-Chao Chondrosarcoma of the toe: A case report and literature review |
title | Chondrosarcoma of the toe: A case report and literature review |
title_full | Chondrosarcoma of the toe: A case report and literature review |
title_fullStr | Chondrosarcoma of the toe: A case report and literature review |
title_full_unstemmed | Chondrosarcoma of the toe: A case report and literature review |
title_short | Chondrosarcoma of the toe: A case report and literature review |
title_sort | chondrosarcoma of the toe: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477028/ https://www.ncbi.nlm.nih.gov/pubmed/36157642 http://dx.doi.org/10.12998/wjcc.v10.i25.9132 |
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