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A Case of Large Solitary Fibrous Tumor in the Retroperitoneum
Solitary fibrous tumor (SFT) is a rare spindle cell neoplasm mainly originated in the pleural cavity. We report here an unusual case of a large SFT in the retroperitoneum. A 27-year-old female complaining of a palpable mass in the right flank with dull pain was admitted to our hospital with the diag...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3785379/ https://www.ncbi.nlm.nih.gov/pubmed/24179368 |
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author | Nomura, Takeo Satoh, Ryuta Kashima, Kenji Yamasaki, Mutsushi Hirai, Kenichi Satoh, Fuminori Mimata, Hiromitsu |
author_facet | Nomura, Takeo Satoh, Ryuta Kashima, Kenji Yamasaki, Mutsushi Hirai, Kenichi Satoh, Fuminori Mimata, Hiromitsu |
author_sort | Nomura, Takeo |
collection | PubMed |
description | Solitary fibrous tumor (SFT) is a rare spindle cell neoplasm mainly originated in the pleural cavity. We report here an unusual case of a large SFT in the retroperitoneum. A 27-year-old female complaining of a palpable mass in the right flank with dull pain was admitted to our hospital with the diagnosis of right retroperitoneal tumor. Computed tomography (CT) and magnetic resonance imaging (MRI) showed a large retroperitoneal tumor arising from latissimus dorsi muscle. Surgical findings revealed a partly encapsulated tumor and complete resection of tumor concomitantly with right kidney, 11th and 12th ribs, and diaphragm was performed. Pathological examination demonstrated the tumor to be composed of increased mitotic activity and cellularity of spindle cells with a collagenous matrix. Immunohistochemical staining was positive for CD34, vimentin, and basic fibroblast growth factor (bFGF) and negative for CD31, cytokeratin, desmin, S-100p, smooth muscle actin, Bcl-2, and insulin-like growth factor (IGF) with Ki-67 labeling index of 0.1%. Based on pathological features, diagnosis of SFT in the retroperitoneum was confirmed. To our knowledge, this is the first report of an SFT arising from latissimus dorsi muscle and it is important to include SFT in the differential diagnosis of retroperitoneal tumors that caused considerable diagnostic problems due to its unusual site of origin. |
format | Online Article Text |
id | pubmed-3785379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-37853792013-10-31 A Case of Large Solitary Fibrous Tumor in the Retroperitoneum Nomura, Takeo Satoh, Ryuta Kashima, Kenji Yamasaki, Mutsushi Hirai, Kenichi Satoh, Fuminori Mimata, Hiromitsu Clin Med Case Rep Case Report Solitary fibrous tumor (SFT) is a rare spindle cell neoplasm mainly originated in the pleural cavity. We report here an unusual case of a large SFT in the retroperitoneum. A 27-year-old female complaining of a palpable mass in the right flank with dull pain was admitted to our hospital with the diagnosis of right retroperitoneal tumor. Computed tomography (CT) and magnetic resonance imaging (MRI) showed a large retroperitoneal tumor arising from latissimus dorsi muscle. Surgical findings revealed a partly encapsulated tumor and complete resection of tumor concomitantly with right kidney, 11th and 12th ribs, and diaphragm was performed. Pathological examination demonstrated the tumor to be composed of increased mitotic activity and cellularity of spindle cells with a collagenous matrix. Immunohistochemical staining was positive for CD34, vimentin, and basic fibroblast growth factor (bFGF) and negative for CD31, cytokeratin, desmin, S-100p, smooth muscle actin, Bcl-2, and insulin-like growth factor (IGF) with Ki-67 labeling index of 0.1%. Based on pathological features, diagnosis of SFT in the retroperitoneum was confirmed. To our knowledge, this is the first report of an SFT arising from latissimus dorsi muscle and it is important to include SFT in the differential diagnosis of retroperitoneal tumors that caused considerable diagnostic problems due to its unusual site of origin. Libertas Academica 2009-03-23 /pmc/articles/PMC3785379/ /pubmed/24179368 Text en © 2009 by the authors http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Case Report Nomura, Takeo Satoh, Ryuta Kashima, Kenji Yamasaki, Mutsushi Hirai, Kenichi Satoh, Fuminori Mimata, Hiromitsu A Case of Large Solitary Fibrous Tumor in the Retroperitoneum |
title | A Case of Large Solitary Fibrous Tumor in the Retroperitoneum |
title_full | A Case of Large Solitary Fibrous Tumor in the Retroperitoneum |
title_fullStr | A Case of Large Solitary Fibrous Tumor in the Retroperitoneum |
title_full_unstemmed | A Case of Large Solitary Fibrous Tumor in the Retroperitoneum |
title_short | A Case of Large Solitary Fibrous Tumor in the Retroperitoneum |
title_sort | case of large solitary fibrous tumor in the retroperitoneum |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3785379/ https://www.ncbi.nlm.nih.gov/pubmed/24179368 |
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