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Fibromyxoid sarcoma of the leg

A 48-year-old female with an atypical plaque-like lesion of the lower leg is presented in this article. Histologic investigation revealed a rare low-grade fibromyxoid sarcoma (pT1a cN0 cM0; stage Ia) of suprafascial localization. Staging of the patient did not reveal metastatic spread. The tumor was...

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Detalles Bibliográficos
Autores principales: Wollina, Uwe, Runge, Juliane, Schönlebe, Jaqueline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481414/
https://www.ncbi.nlm.nih.gov/pubmed/23130188
http://dx.doi.org/10.4103/2229-5178.73254
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author Wollina, Uwe
Runge, Juliane
Schönlebe, Jaqueline
author_facet Wollina, Uwe
Runge, Juliane
Schönlebe, Jaqueline
author_sort Wollina, Uwe
collection PubMed
description A 48-year-old female with an atypical plaque-like lesion of the lower leg is presented in this article. Histologic investigation revealed a rare low-grade fibromyxoid sarcoma (pT1a cN0 cM0; stage Ia) of suprafascial localization. Staging of the patient did not reveal metastatic spread. The tumor was surgically removed with wide safety margins. The defect was closed using a mesh graft transplant and vacuum-assisted closure. Healing was complete. Regular follow-up for at least 5 years is recommended. Besides the rareness of this tumor, this case is also remarkable because of the localization on the lower leg and the suprafascial soft tissue.
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spelling pubmed-34814142012-11-05 Fibromyxoid sarcoma of the leg Wollina, Uwe Runge, Juliane Schönlebe, Jaqueline Indian Dermatol Online J Case Report A 48-year-old female with an atypical plaque-like lesion of the lower leg is presented in this article. Histologic investigation revealed a rare low-grade fibromyxoid sarcoma (pT1a cN0 cM0; stage Ia) of suprafascial localization. Staging of the patient did not reveal metastatic spread. The tumor was surgically removed with wide safety margins. The defect was closed using a mesh graft transplant and vacuum-assisted closure. Healing was complete. Regular follow-up for at least 5 years is recommended. Besides the rareness of this tumor, this case is also remarkable because of the localization on the lower leg and the suprafascial soft tissue. Medknow Publications & Media Pvt Ltd 2010 /pmc/articles/PMC3481414/ /pubmed/23130188 http://dx.doi.org/10.4103/2229-5178.73254 Text en Copyright: © Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Wollina, Uwe
Runge, Juliane
Schönlebe, Jaqueline
Fibromyxoid sarcoma of the leg
title Fibromyxoid sarcoma of the leg
title_full Fibromyxoid sarcoma of the leg
title_fullStr Fibromyxoid sarcoma of the leg
title_full_unstemmed Fibromyxoid sarcoma of the leg
title_short Fibromyxoid sarcoma of the leg
title_sort fibromyxoid sarcoma of the leg
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481414/
https://www.ncbi.nlm.nih.gov/pubmed/23130188
http://dx.doi.org/10.4103/2229-5178.73254
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