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Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review
BACKGROUND: Temporalis muscle hypertrophy is a rare entity of masticatory muscle hypertrophy. All types of masticatory muscle hypertrophies have been documented of which temporalis muscle hypertrophy is one. Temporalis muscle hypertrophy is most commonly bilateral and usually associated with other t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817789/ https://www.ncbi.nlm.nih.gov/pubmed/29458353 http://dx.doi.org/10.1186/s12887-018-1061-7 |
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author | Ranasinghe, Jagath C. Wickramasinghe, Chandani Rodrigo, Ganganath |
author_facet | Ranasinghe, Jagath C. Wickramasinghe, Chandani Rodrigo, Ganganath |
author_sort | Ranasinghe, Jagath C. |
collection | PubMed |
description | BACKGROUND: Temporalis muscle hypertrophy is a rare entity of masticatory muscle hypertrophy. All types of masticatory muscle hypertrophies have been documented of which temporalis muscle hypertrophy is one. Temporalis muscle hypertrophy is most commonly bilateral and usually associated with other types of masticatory muscles hypertrophy such as masseter or pterygoid hypertrophy. However, isolated unilateral temporalis muscle hypertrophy is extremely rare and only 9 cases have been reported to date in English literature since 1990 with only two patients less than 18 years. There is no exact etiology identified and the diagnosis is made by muscle biopsy combined with imaging study to exclude other possibilities. Age at presentation is ranges from 15 to 65 years with involvement of both sexes. We report the youngest child who is a seven year old girl with right side isolated unilateral temporalis muscle hypertrophy. CASE PRESENTATION: In this patient, we discuss the youngest child with isolated unilateral temporalis muscle hypertrophy and literature review to date. The patient is a seven year old female presenting with painless swelling of the right temporalis muscle. There had no features of inflammation, trauma, neoplasm or history of parafunctions such as bruxism. The child was not complaining significantly headache or visual disturbances as well. She had undergone radiological assessment with ultrasound scan and contrast MRI. The diagnosis was confirmed by muscle biopsy which shows normal muscle architecture. She was managed conservatively with regular follow up. CONCLUSION: Isolated unilateral temporalis muscle hypertrophy is extremely rare in children. However this case raises the importance of considering alternative diagnoses despite the condition being rare in the pediatric population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12887-018-1061-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5817789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58177892018-02-23 Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review Ranasinghe, Jagath C. Wickramasinghe, Chandani Rodrigo, Ganganath BMC Pediatr Case Report BACKGROUND: Temporalis muscle hypertrophy is a rare entity of masticatory muscle hypertrophy. All types of masticatory muscle hypertrophies have been documented of which temporalis muscle hypertrophy is one. Temporalis muscle hypertrophy is most commonly bilateral and usually associated with other types of masticatory muscles hypertrophy such as masseter or pterygoid hypertrophy. However, isolated unilateral temporalis muscle hypertrophy is extremely rare and only 9 cases have been reported to date in English literature since 1990 with only two patients less than 18 years. There is no exact etiology identified and the diagnosis is made by muscle biopsy combined with imaging study to exclude other possibilities. Age at presentation is ranges from 15 to 65 years with involvement of both sexes. We report the youngest child who is a seven year old girl with right side isolated unilateral temporalis muscle hypertrophy. CASE PRESENTATION: In this patient, we discuss the youngest child with isolated unilateral temporalis muscle hypertrophy and literature review to date. The patient is a seven year old female presenting with painless swelling of the right temporalis muscle. There had no features of inflammation, trauma, neoplasm or history of parafunctions such as bruxism. The child was not complaining significantly headache or visual disturbances as well. She had undergone radiological assessment with ultrasound scan and contrast MRI. The diagnosis was confirmed by muscle biopsy which shows normal muscle architecture. She was managed conservatively with regular follow up. CONCLUSION: Isolated unilateral temporalis muscle hypertrophy is extremely rare in children. However this case raises the importance of considering alternative diagnoses despite the condition being rare in the pediatric population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12887-018-1061-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-19 /pmc/articles/PMC5817789/ /pubmed/29458353 http://dx.doi.org/10.1186/s12887-018-1061-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Ranasinghe, Jagath C. Wickramasinghe, Chandani Rodrigo, Ganganath Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
title | Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
title_full | Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
title_fullStr | Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
title_full_unstemmed | Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
title_short | Isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
title_sort | isolated unilateral temporalis muscle hypertrophy in a child: a case report with literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817789/ https://www.ncbi.nlm.nih.gov/pubmed/29458353 http://dx.doi.org/10.1186/s12887-018-1061-7 |
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