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Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature
BACKGROUND: Leiomyosarcoma (LMS) is a malignant tumour formed of cells with distinct smooth muscle features. Leiomyosarcomas rarely metastasise to the oral cavity and this literature review details all reported cases of metastasis to the mandible found in the literature. This offers a unique perspec...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704575/ https://www.ncbi.nlm.nih.gov/pubmed/29179757 http://dx.doi.org/10.1186/s12905-017-0472-1 |
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author | Hope, Isabel Morton, Karen Newlands, Carrie Butler-Manuel, Simon Madhuri, Thumuluru Kavitha |
author_facet | Hope, Isabel Morton, Karen Newlands, Carrie Butler-Manuel, Simon Madhuri, Thumuluru Kavitha |
author_sort | Hope, Isabel |
collection | PubMed |
description | BACKGROUND: Leiomyosarcoma (LMS) is a malignant tumour formed of cells with distinct smooth muscle features. Leiomyosarcomas rarely metastasise to the oral cavity and this literature review details all reported cases of metastasis to the mandible found in the literature. This offers a unique perspective by specifying mandible as the site of metastasis of leiomyosarcoma. CASE PRESENTATION: A 53-year-old female presented to her General Practitioner (GP) with heavy menstrual bleeding and was diagnosed with multiple fibroids. Folowing a hysterectomy and removal of both tubes and ovaries for these symptomatic uterine fibroids, an incidental diagnosis of low grade leiomyosarcoma was made. A CT scan found no evidence of residual or metastatic disease and no further treatment was deemed necessary. 6 months later she presented to A & E with a numb lower lip but it took another 6 months for the diagnosis of metastatic LMS to the mandible to be made. DISCUSSION: Leiomyosarcomas are aggressive tumours which are liable to metastasise and therefore have a poor prognosis. An extensive literature review was undertaken to explore the frequency of metastasis in the maxillo-facial region. CONCLUSIONS: Although metastasis to the oral region is very rare as suggested from the literature review, when patients present with unusual symptoms after a diagnosis of LMS, physicians should be aware of the possibility of LMS metastases. |
format | Online Article Text |
id | pubmed-5704575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57045752017-12-05 Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature Hope, Isabel Morton, Karen Newlands, Carrie Butler-Manuel, Simon Madhuri, Thumuluru Kavitha BMC Womens Health Case Report BACKGROUND: Leiomyosarcoma (LMS) is a malignant tumour formed of cells with distinct smooth muscle features. Leiomyosarcomas rarely metastasise to the oral cavity and this literature review details all reported cases of metastasis to the mandible found in the literature. This offers a unique perspective by specifying mandible as the site of metastasis of leiomyosarcoma. CASE PRESENTATION: A 53-year-old female presented to her General Practitioner (GP) with heavy menstrual bleeding and was diagnosed with multiple fibroids. Folowing a hysterectomy and removal of both tubes and ovaries for these symptomatic uterine fibroids, an incidental diagnosis of low grade leiomyosarcoma was made. A CT scan found no evidence of residual or metastatic disease and no further treatment was deemed necessary. 6 months later she presented to A & E with a numb lower lip but it took another 6 months for the diagnosis of metastatic LMS to the mandible to be made. DISCUSSION: Leiomyosarcomas are aggressive tumours which are liable to metastasise and therefore have a poor prognosis. An extensive literature review was undertaken to explore the frequency of metastasis in the maxillo-facial region. CONCLUSIONS: Although metastasis to the oral region is very rare as suggested from the literature review, when patients present with unusual symptoms after a diagnosis of LMS, physicians should be aware of the possibility of LMS metastases. BioMed Central 2017-11-28 /pmc/articles/PMC5704575/ /pubmed/29179757 http://dx.doi.org/10.1186/s12905-017-0472-1 Text en © The Author(s). 2017 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 Hope, Isabel Morton, Karen Newlands, Carrie Butler-Manuel, Simon Madhuri, Thumuluru Kavitha Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
title | Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
title_full | Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
title_fullStr | Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
title_full_unstemmed | Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
title_short | Lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
title_sort | lockjaw from a metastatic uterine leiomyosarcoma- case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704575/ https://www.ncbi.nlm.nih.gov/pubmed/29179757 http://dx.doi.org/10.1186/s12905-017-0472-1 |
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