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Spindle cell rhabdomyosarcoma in the adult: A rare case report
Spindle cell/sclerosing rhabdomyosarcoma (RMS) is an uncommon type of RMS and has been classified as a separate entity by the WHO in 2013. It affects both children and adults with a greater incidence in males. These tumors can pose a diagnostic challenge and can be difficult to differentiate from ot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017831/ https://www.ncbi.nlm.nih.gov/pubmed/35450245 http://dx.doi.org/10.4103/jomfp.jomfp_251_21 |
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author | Jakkampudi, Ashlesha Kaliyath, Sajitha Hegde, Padmaraj Mathias, Michelle Shetty, Vikram |
author_facet | Jakkampudi, Ashlesha Kaliyath, Sajitha Hegde, Padmaraj Mathias, Michelle Shetty, Vikram |
author_sort | Jakkampudi, Ashlesha |
collection | PubMed |
description | Spindle cell/sclerosing rhabdomyosarcoma (RMS) is an uncommon type of RMS and has been classified as a separate entity by the WHO in 2013. It affects both children and adults with a greater incidence in males. These tumors can pose a diagnostic challenge and can be difficult to differentiate from other spindle cell malignant tumors in the head and neck. Here, we report a case of spindle cell/sclerosing RMS in a young woman presenting with a swelling on the left side of the face of 3 months duration. A careful correlation with the radiographic images, histopathological findings and immunohistochemistry helped to arrive at a diagnosis. |
format | Online Article Text |
id | pubmed-9017831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-90178312022-04-20 Spindle cell rhabdomyosarcoma in the adult: A rare case report Jakkampudi, Ashlesha Kaliyath, Sajitha Hegde, Padmaraj Mathias, Michelle Shetty, Vikram J Oral Maxillofac Pathol Case Report Spindle cell/sclerosing rhabdomyosarcoma (RMS) is an uncommon type of RMS and has been classified as a separate entity by the WHO in 2013. It affects both children and adults with a greater incidence in males. These tumors can pose a diagnostic challenge and can be difficult to differentiate from other spindle cell malignant tumors in the head and neck. Here, we report a case of spindle cell/sclerosing RMS in a young woman presenting with a swelling on the left side of the face of 3 months duration. A careful correlation with the radiographic images, histopathological findings and immunohistochemistry helped to arrive at a diagnosis. Wolters Kluwer - Medknow 2022-02 2022-02-28 /pmc/articles/PMC9017831/ /pubmed/35450245 http://dx.doi.org/10.4103/jomfp.jomfp_251_21 Text en Copyright: © 2022 Journal of Oral and Maxillofacial Pathology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Jakkampudi, Ashlesha Kaliyath, Sajitha Hegde, Padmaraj Mathias, Michelle Shetty, Vikram Spindle cell rhabdomyosarcoma in the adult: A rare case report |
title | Spindle cell rhabdomyosarcoma in the adult: A rare case report |
title_full | Spindle cell rhabdomyosarcoma in the adult: A rare case report |
title_fullStr | Spindle cell rhabdomyosarcoma in the adult: A rare case report |
title_full_unstemmed | Spindle cell rhabdomyosarcoma in the adult: A rare case report |
title_short | Spindle cell rhabdomyosarcoma in the adult: A rare case report |
title_sort | spindle cell rhabdomyosarcoma in the adult: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017831/ https://www.ncbi.nlm.nih.gov/pubmed/35450245 http://dx.doi.org/10.4103/jomfp.jomfp_251_21 |
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