Cargando…

Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review

Chondromyxoid fibroma (CMF) is the least commonly occurring bone tumor of cartilaginous origin. It is usually situated in the metaphysis of long bones of the lower limbs. Localization of the tumor in the skull is extremely rare. The definitive diagnosis is challenging and depends on radiological and...

Descripción completa

Detalles Bibliográficos
Autores principales: Elsamanody, Ahmed, Van den Aardweg, Maaike, Smits, Alexander, Willems, Stefan, Topsakal, Vedat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The European Academy of Otology and Neurotology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224415/
https://www.ncbi.nlm.nih.gov/pubmed/32209521
http://dx.doi.org/10.5152/iao.2019.6911
_version_ 1783533893386764288
author Elsamanody, Ahmed
Van den Aardweg, Maaike
Smits, Alexander
Willems, Stefan
Topsakal, Vedat
author_facet Elsamanody, Ahmed
Van den Aardweg, Maaike
Smits, Alexander
Willems, Stefan
Topsakal, Vedat
author_sort Elsamanody, Ahmed
collection PubMed
description Chondromyxoid fibroma (CMF) is the least commonly occurring bone tumor of cartilaginous origin. It is usually situated in the metaphysis of long bones of the lower limbs. Localization of the tumor in the skull is extremely rare. The definitive diagnosis is challenging and depends on radiological and histological examinations. To the best of our knowledge, only 14 cases of CMF involving the temporal bone have been reported to date, 7 of which were within the mastoid. The most common clinical symptom is headache; however, these symptoms vary greatly according to site, size, and extension of the lesion. Surgical removal is the treatment of choice. A literature review of the diagnostic challenges, histological difficulties in differential diagnosis, imaging, clinical features, and recommended modalities of treatment have been discussed in the present case.
format Online
Article
Text
id pubmed-7224415
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The European Academy of Otology and Neurotology
record_format MEDLINE/PubMed
spelling pubmed-72244152020-05-15 Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review Elsamanody, Ahmed Van den Aardweg, Maaike Smits, Alexander Willems, Stefan Topsakal, Vedat J Int Adv Otol Review Chondromyxoid fibroma (CMF) is the least commonly occurring bone tumor of cartilaginous origin. It is usually situated in the metaphysis of long bones of the lower limbs. Localization of the tumor in the skull is extremely rare. The definitive diagnosis is challenging and depends on radiological and histological examinations. To the best of our knowledge, only 14 cases of CMF involving the temporal bone have been reported to date, 7 of which were within the mastoid. The most common clinical symptom is headache; however, these symptoms vary greatly according to site, size, and extension of the lesion. Surgical removal is the treatment of choice. A literature review of the diagnostic challenges, histological difficulties in differential diagnosis, imaging, clinical features, and recommended modalities of treatment have been discussed in the present case. The European Academy of Otology and Neurotology 2020-04 2020-03-20 /pmc/articles/PMC7224415/ /pubmed/32209521 http://dx.doi.org/10.5152/iao.2019.6911 Text en © Copyright 2020 The European Academy of Otology and Neurotology https://creativecommons.org/licenses/by-nc/4.0/Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Review
Elsamanody, Ahmed
Van den Aardweg, Maaike
Smits, Alexander
Willems, Stefan
Topsakal, Vedat
Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review
title Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review
title_full Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review
title_fullStr Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review
title_full_unstemmed Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review
title_short Chondromyxoid Fibroma of the Mastoid: A Rare Entity with Comprehensive Literature Review
title_sort chondromyxoid fibroma of the mastoid: a rare entity with comprehensive literature review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224415/
https://www.ncbi.nlm.nih.gov/pubmed/32209521
http://dx.doi.org/10.5152/iao.2019.6911
work_keys_str_mv AT elsamanodyahmed chondromyxoidfibromaofthemastoidarareentitywithcomprehensiveliteraturereview
AT vandenaardwegmaaike chondromyxoidfibromaofthemastoidarareentitywithcomprehensiveliteraturereview
AT smitsalexander chondromyxoidfibromaofthemastoidarareentitywithcomprehensiveliteraturereview
AT willemsstefan chondromyxoidfibromaofthemastoidarareentitywithcomprehensiveliteraturereview
AT topsakalvedat chondromyxoidfibromaofthemastoidarareentitywithcomprehensiveliteraturereview