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Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion

Collagenous fibroma (desmoplastic fibroblastoma) is a recently described rare benign tumor affecting mainly males in the fifth through seventh decades. This tumor occurs predominantly in the peripheral sites, with predilection for upper and lower extremities. The patients present with a painless mas...

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Detalles Bibliográficos
Autores principales: Osipov, Vladimir, Carrera, Guillermo F.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688648/
https://www.ncbi.nlm.nih.gov/pubmed/19503798
http://dx.doi.org/10.1155/2009/682687
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author Osipov, Vladimir
Carrera, Guillermo F.
author_facet Osipov, Vladimir
Carrera, Guillermo F.
author_sort Osipov, Vladimir
collection PubMed
description Collagenous fibroma (desmoplastic fibroblastoma) is a recently described rare benign tumor affecting mainly males in the fifth through seventh decades. This tumor occurs predominantly in the peripheral sites, with predilection for upper and lower extremities. The patients present with a painless mass of involving subcutis, with one quarter of all cases involving skeletal muscle. Both radiographically and histologically these tumors are well-circumscribed small lesions from one to several centimeters in diameter, though lesions as large as 20 cm have been reported. We report a case of collagenous fibroma presenting symptomatically as a 2.4 cm mass within the pedicle and adjacent transverse process of the L5 vertebral segment. Bone erosion by desmoplastic fibroblastoma is very rare event. This tumor should be in the differential diagnosis of the soft tissue lesions presenting with bony erosion.
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spelling pubmed-26886482009-06-04 Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion Osipov, Vladimir Carrera, Guillermo F. Sarcoma Case Report Collagenous fibroma (desmoplastic fibroblastoma) is a recently described rare benign tumor affecting mainly males in the fifth through seventh decades. This tumor occurs predominantly in the peripheral sites, with predilection for upper and lower extremities. The patients present with a painless mass of involving subcutis, with one quarter of all cases involving skeletal muscle. Both radiographically and histologically these tumors are well-circumscribed small lesions from one to several centimeters in diameter, though lesions as large as 20 cm have been reported. We report a case of collagenous fibroma presenting symptomatically as a 2.4 cm mass within the pedicle and adjacent transverse process of the L5 vertebral segment. Bone erosion by desmoplastic fibroblastoma is very rare event. This tumor should be in the differential diagnosis of the soft tissue lesions presenting with bony erosion. Hindawi Publishing Corporation 2009 2009-05-27 /pmc/articles/PMC2688648/ /pubmed/19503798 http://dx.doi.org/10.1155/2009/682687 Text en Copyright © 2009 V. Osipov and G. F. Carrera. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Osipov, Vladimir
Carrera, Guillermo F.
Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion
title Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion
title_full Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion
title_fullStr Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion
title_full_unstemmed Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion
title_short Collagenous Fibroma (Desmoplastic Fibroblastoma) with Vertebral Body Erosion
title_sort collagenous fibroma (desmoplastic fibroblastoma) with vertebral body erosion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688648/
https://www.ncbi.nlm.nih.gov/pubmed/19503798
http://dx.doi.org/10.1155/2009/682687
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