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Primary leiomyosarcoma of the submandibular gland: a case report
BACKGROUND: Leiomyosarcoma is a rare malignant mesenchymal tumor that represents 5–7 % of all soft tissue sarcomas. The occurrence of this tumor in the salivary glands is exceptional. Only five cases are reported in the submandibular gland. CASE PRESENTATION: A 65-year-old white Moroccan woman prese...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678697/ https://www.ncbi.nlm.nih.gov/pubmed/26674090 http://dx.doi.org/10.1186/s12907-015-0022-4 |
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author | El Ochi, Mohamed Reda Chahdi, Hafsa Rharrassi, Issam Albouzidi, Abderrahman Oukabli, Mohamed |
author_facet | El Ochi, Mohamed Reda Chahdi, Hafsa Rharrassi, Issam Albouzidi, Abderrahman Oukabli, Mohamed |
author_sort | El Ochi, Mohamed Reda |
collection | PubMed |
description | BACKGROUND: Leiomyosarcoma is a rare malignant mesenchymal tumor that represents 5–7 % of all soft tissue sarcomas. The occurrence of this tumor in the salivary glands is exceptional. Only five cases are reported in the submandibular gland. CASE PRESENTATION: A 65-year-old white Moroccan woman presented with a history of progressive right submandibular swelling which had grown over a period of 8 months. Clinical examination showed a submandibular painless, mobile and hard mass without cervical lymphadenopathy. Ultrasonography and computed tomography revealed a solid and heterogeneous mass measuring 4 × 2 cm involving the submandibular gland. A resection of the gland was performed. Pathological findings were consistent with primary leiomyosarcoma of the submandibular gland. No recurrence occurred after two months of follow-up. CONCLUSION: Primary leiomyosarcoma of the submandibular gland is an extremely rare mesenchymal tumor. Clinical and radiological features are not specific. Differential diagnosis includes metastatic leiomyosarcoma and gastrointestinal stromal tumor, myoepithelioma, sarcomatoid carcinoma, melanoma and other sarcomas. Little is known about the overall biologic behavior of this tumor, but the prognosis seems to be poor. |
format | Online Article Text |
id | pubmed-4678697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46786972015-12-16 Primary leiomyosarcoma of the submandibular gland: a case report El Ochi, Mohamed Reda Chahdi, Hafsa Rharrassi, Issam Albouzidi, Abderrahman Oukabli, Mohamed BMC Clin Pathol Case Report BACKGROUND: Leiomyosarcoma is a rare malignant mesenchymal tumor that represents 5–7 % of all soft tissue sarcomas. The occurrence of this tumor in the salivary glands is exceptional. Only five cases are reported in the submandibular gland. CASE PRESENTATION: A 65-year-old white Moroccan woman presented with a history of progressive right submandibular swelling which had grown over a period of 8 months. Clinical examination showed a submandibular painless, mobile and hard mass without cervical lymphadenopathy. Ultrasonography and computed tomography revealed a solid and heterogeneous mass measuring 4 × 2 cm involving the submandibular gland. A resection of the gland was performed. Pathological findings were consistent with primary leiomyosarcoma of the submandibular gland. No recurrence occurred after two months of follow-up. CONCLUSION: Primary leiomyosarcoma of the submandibular gland is an extremely rare mesenchymal tumor. Clinical and radiological features are not specific. Differential diagnosis includes metastatic leiomyosarcoma and gastrointestinal stromal tumor, myoepithelioma, sarcomatoid carcinoma, melanoma and other sarcomas. Little is known about the overall biologic behavior of this tumor, but the prognosis seems to be poor. BioMed Central 2015-12-15 /pmc/articles/PMC4678697/ /pubmed/26674090 http://dx.doi.org/10.1186/s12907-015-0022-4 Text en © El Ochi et al. 2015 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 El Ochi, Mohamed Reda Chahdi, Hafsa Rharrassi, Issam Albouzidi, Abderrahman Oukabli, Mohamed Primary leiomyosarcoma of the submandibular gland: a case report |
title | Primary leiomyosarcoma of the submandibular gland: a case report |
title_full | Primary leiomyosarcoma of the submandibular gland: a case report |
title_fullStr | Primary leiomyosarcoma of the submandibular gland: a case report |
title_full_unstemmed | Primary leiomyosarcoma of the submandibular gland: a case report |
title_short | Primary leiomyosarcoma of the submandibular gland: a case report |
title_sort | primary leiomyosarcoma of the submandibular gland: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678697/ https://www.ncbi.nlm.nih.gov/pubmed/26674090 http://dx.doi.org/10.1186/s12907-015-0022-4 |
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