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Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm

Solitary fibrous tumour (SFT) is a rare benign tumour that occurs most frequently in the pleura. It is considered rare in soft tissues. We report a case of a middle-aged woman that presented a solitary fibrous tumor of gluteus. The tumour was composed of mesenchymal spindle-shaped cells positive for...

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Autores principales: Occhionorelli, Savino, Pigato, Ilaria, Malvicini, Enzo, Pascale, Giovanni, Stano, Rocco, Rinaldi, Rosa, Vasquez, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917280/
https://www.ncbi.nlm.nih.gov/pubmed/27333919
http://dx.doi.org/10.1093/jscr/rjw111
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author Occhionorelli, Savino
Pigato, Ilaria
Malvicini, Enzo
Pascale, Giovanni
Stano, Rocco
Rinaldi, Rosa
Vasquez, Giorgio
author_facet Occhionorelli, Savino
Pigato, Ilaria
Malvicini, Enzo
Pascale, Giovanni
Stano, Rocco
Rinaldi, Rosa
Vasquez, Giorgio
author_sort Occhionorelli, Savino
collection PubMed
description Solitary fibrous tumour (SFT) is a rare benign tumour that occurs most frequently in the pleura. It is considered rare in soft tissues. We report a case of a middle-aged woman that presented a solitary fibrous tumor of gluteus. The tumour was composed of mesenchymal spindle-shaped cells positive for CD34 and bcl-2. Although rare, SFT should be included in the differential diagnosis of mesenchymal soft tissue tumours. The clinical presentation and imaging can be helpful for a better pre-operative diagnosis.
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spelling pubmed-49172802016-06-23 Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm Occhionorelli, Savino Pigato, Ilaria Malvicini, Enzo Pascale, Giovanni Stano, Rocco Rinaldi, Rosa Vasquez, Giorgio J Surg Case Rep Case Report Solitary fibrous tumour (SFT) is a rare benign tumour that occurs most frequently in the pleura. It is considered rare in soft tissues. We report a case of a middle-aged woman that presented a solitary fibrous tumor of gluteus. The tumour was composed of mesenchymal spindle-shaped cells positive for CD34 and bcl-2. Although rare, SFT should be included in the differential diagnosis of mesenchymal soft tissue tumours. The clinical presentation and imaging can be helpful for a better pre-operative diagnosis. Oxford University Press 2016-06-22 /pmc/articles/PMC4917280/ /pubmed/27333919 http://dx.doi.org/10.1093/jscr/rjw111 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2016. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Occhionorelli, Savino
Pigato, Ilaria
Malvicini, Enzo
Pascale, Giovanni
Stano, Rocco
Rinaldi, Rosa
Vasquez, Giorgio
Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
title Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
title_full Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
title_fullStr Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
title_full_unstemmed Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
title_short Solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
title_sort solitary fibrous tumour of gluteus: a case report about an uncommon localization of a rare neoplasm
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917280/
https://www.ncbi.nlm.nih.gov/pubmed/27333919
http://dx.doi.org/10.1093/jscr/rjw111
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