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Chondromyxoid fibroma of the temporal bone: A rare entity

Chondromyxoid fibroma (CMF) is the least common benign tumor of the cartilaginous origin. It is very unusual to find these tumors in the skull bones. We report one such case involving the temporal bone. Till date, only nine such cases including this patient, involving the temporal bone have been rep...

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Autores principales: Sharma, Mayur, Velho, Vernon, Binayake, Rachana, Tiwari, Chandranath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611914/
https://www.ncbi.nlm.nih.gov/pubmed/23560012
http://dx.doi.org/10.4103/1817-1745.106483
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author Sharma, Mayur
Velho, Vernon
Binayake, Rachana
Tiwari, Chandranath
author_facet Sharma, Mayur
Velho, Vernon
Binayake, Rachana
Tiwari, Chandranath
author_sort Sharma, Mayur
collection PubMed
description Chondromyxoid fibroma (CMF) is the least common benign tumor of the cartilaginous origin. It is very unusual to find these tumors in the skull bones. We report one such case involving the temporal bone. Till date, only nine such cases including this patient, involving the temporal bone have been reported to the best of our knowledge. Grant Medical College and Sir J.J Group of Hospitals, Byculla, Mumbai, Maharashtra, India. A 12-year-old female patient presented with a history of headache associated with left earache of 1 month duration. This was followed by swelling over the left preauricular region 15 days later. Imaging was suggestive of an expansile lesion involving the squamous part of the left temporal bone with calcifications suggestive of a benign chondroid lesion. The patient was operated upon with left temporal incision and complete excision of the lesion. The patient had relief from headache, earache and swelling, with no evidence of new neurological deficit in the post-operative period. CMF of the skull bone is an extremely rare tumor. Differential diagnosis should be kept in mind, especially in cases of calcified lesions and includes chordoma, chondroid chondroma, and low-grade myxoid chondrosarcoma. En-bloc complete excision should be the aim to achieve cure.
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spelling pubmed-36119142013-04-04 Chondromyxoid fibroma of the temporal bone: A rare entity Sharma, Mayur Velho, Vernon Binayake, Rachana Tiwari, Chandranath J Pediatr Neurosci Case Report Chondromyxoid fibroma (CMF) is the least common benign tumor of the cartilaginous origin. It is very unusual to find these tumors in the skull bones. We report one such case involving the temporal bone. Till date, only nine such cases including this patient, involving the temporal bone have been reported to the best of our knowledge. Grant Medical College and Sir J.J Group of Hospitals, Byculla, Mumbai, Maharashtra, India. A 12-year-old female patient presented with a history of headache associated with left earache of 1 month duration. This was followed by swelling over the left preauricular region 15 days later. Imaging was suggestive of an expansile lesion involving the squamous part of the left temporal bone with calcifications suggestive of a benign chondroid lesion. The patient was operated upon with left temporal incision and complete excision of the lesion. The patient had relief from headache, earache and swelling, with no evidence of new neurological deficit in the post-operative period. CMF of the skull bone is an extremely rare tumor. Differential diagnosis should be kept in mind, especially in cases of calcified lesions and includes chordoma, chondroid chondroma, and low-grade myxoid chondrosarcoma. En-bloc complete excision should be the aim to achieve cure. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3611914/ /pubmed/23560012 http://dx.doi.org/10.4103/1817-1745.106483 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharma, Mayur
Velho, Vernon
Binayake, Rachana
Tiwari, Chandranath
Chondromyxoid fibroma of the temporal bone: A rare entity
title Chondromyxoid fibroma of the temporal bone: A rare entity
title_full Chondromyxoid fibroma of the temporal bone: A rare entity
title_fullStr Chondromyxoid fibroma of the temporal bone: A rare entity
title_full_unstemmed Chondromyxoid fibroma of the temporal bone: A rare entity
title_short Chondromyxoid fibroma of the temporal bone: A rare entity
title_sort chondromyxoid fibroma of the temporal bone: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611914/
https://www.ncbi.nlm.nih.gov/pubmed/23560012
http://dx.doi.org/10.4103/1817-1745.106483
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