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Temporal Bone Chondroblastoma: a Rare Entity
INTRODUCTION: Chondroblastoma is an uncommon benign, locally destructive tumor that usually arises from epiphyses of the long bones. Temporal bone chondroblastoma is an extremely rare occurrence. Chondroblastoma arise from immature cartilage cells and it may display certain malignant features by inv...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academy of Medical Sciences of Bosnia and Herzegovina
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520067/ https://www.ncbi.nlm.nih.gov/pubmed/33041452 http://dx.doi.org/10.5455/medarh.2020.74.312-314 |
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author | Yusof, Asfa Najmi Mohamad Thong, How Kit Kamalden, Tengku Mohamed Izam Tengku |
author_facet | Yusof, Asfa Najmi Mohamad Thong, How Kit Kamalden, Tengku Mohamed Izam Tengku |
author_sort | Yusof, Asfa Najmi Mohamad |
collection | PubMed |
description | INTRODUCTION: Chondroblastoma is an uncommon benign, locally destructive tumor that usually arises from epiphyses of the long bones. Temporal bone chondroblastoma is an extremely rare occurrence. Chondroblastoma arise from immature cartilage cells and it may display certain malignant features by invading surrounding structures and metastasizing to adjacent sites. AIM: To present a case of extradural temporal bone chondroblastoma and discuss the clinical presentation, radiographic findings, histology and particularly the surgical management of the case. CASE REPORT: We report a case of a 31-year-old man who presented with a painless left temporal swelling and left sided hearing loss for four months. Computed tomography (CT) scan revealed an aggressive mass involving the left preauricular region with temporal mastoid bone erosion. Magnetic resonance imaging (MRI) showed an extra-axial left temporal mastoid mass pushing the left temporal lobe superiorly. The patient underwent complete excision of the temporal bone tumor. The final histopathological diagnosis was in keeping with chondroblastoma. CONCLUSION: Temporal bone chondroblastoma is rare but an aggressive condition. Complete tumor resection via an appropriate approach that enables adequate exposure will lead to a favorable outcome. |
format | Online Article Text |
id | pubmed-7520067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Academy of Medical Sciences of Bosnia and Herzegovina |
record_format | MEDLINE/PubMed |
spelling | pubmed-75200672020-10-08 Temporal Bone Chondroblastoma: a Rare Entity Yusof, Asfa Najmi Mohamad Thong, How Kit Kamalden, Tengku Mohamed Izam Tengku Med Arch Case Report INTRODUCTION: Chondroblastoma is an uncommon benign, locally destructive tumor that usually arises from epiphyses of the long bones. Temporal bone chondroblastoma is an extremely rare occurrence. Chondroblastoma arise from immature cartilage cells and it may display certain malignant features by invading surrounding structures and metastasizing to adjacent sites. AIM: To present a case of extradural temporal bone chondroblastoma and discuss the clinical presentation, radiographic findings, histology and particularly the surgical management of the case. CASE REPORT: We report a case of a 31-year-old man who presented with a painless left temporal swelling and left sided hearing loss for four months. Computed tomography (CT) scan revealed an aggressive mass involving the left preauricular region with temporal mastoid bone erosion. Magnetic resonance imaging (MRI) showed an extra-axial left temporal mastoid mass pushing the left temporal lobe superiorly. The patient underwent complete excision of the temporal bone tumor. The final histopathological diagnosis was in keeping with chondroblastoma. CONCLUSION: Temporal bone chondroblastoma is rare but an aggressive condition. Complete tumor resection via an appropriate approach that enables adequate exposure will lead to a favorable outcome. Academy of Medical Sciences of Bosnia and Herzegovina 2020-08 /pmc/articles/PMC7520067/ /pubmed/33041452 http://dx.doi.org/10.5455/medarh.2020.74.312-314 Text en © 2020 Asfa Najmi Mohamad Yusof, How Kit Thong, Tengku Mohamed Izam Tengku Kamalden http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Yusof, Asfa Najmi Mohamad Thong, How Kit Kamalden, Tengku Mohamed Izam Tengku Temporal Bone Chondroblastoma: a Rare Entity |
title | Temporal Bone Chondroblastoma: a Rare Entity |
title_full | Temporal Bone Chondroblastoma: a Rare Entity |
title_fullStr | Temporal Bone Chondroblastoma: a Rare Entity |
title_full_unstemmed | Temporal Bone Chondroblastoma: a Rare Entity |
title_short | Temporal Bone Chondroblastoma: a Rare Entity |
title_sort | temporal bone chondroblastoma: a rare entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520067/ https://www.ncbi.nlm.nih.gov/pubmed/33041452 http://dx.doi.org/10.5455/medarh.2020.74.312-314 |
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