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Malignant solitary fibrous tumor in the extremity: Cytopathologic findings
Malignant solitary fibrous tumor (SFT) is an extremely rare neoplasm. There are only rare published accounts of the cytopathologic features of this tumor. We report a case of a 59-year-old woman presented with a 10-year history of a right thigh mass. A preoperative fine needle aspiration (FNA) was p...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391798/ https://www.ncbi.nlm.nih.gov/pubmed/22787298 http://dx.doi.org/10.4103/0970-9371.97160 |
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author | Khanchel, Fatma Driss, Maha Mrad, Karima Romdhane, Khaled Ben |
author_facet | Khanchel, Fatma Driss, Maha Mrad, Karima Romdhane, Khaled Ben |
author_sort | Khanchel, Fatma |
collection | PubMed |
description | Malignant solitary fibrous tumor (SFT) is an extremely rare neoplasm. There are only rare published accounts of the cytopathologic features of this tumor. We report a case of a 59-year-old woman presented with a 10-year history of a right thigh mass. A preoperative fine needle aspiration (FNA) was performed. Smears were hypercellular, with cohesive and crowded tissue fragments, haphazard cell arrangements and many single cells. The tumor cells were polymorphous, plump spindled or round with often indented or bare nuclei. A differential diagnosis of low grade sarcoma was favored. The diagnosis of malignant SFT is extremely difficult on FNA and must be included in the differential diagnosis of spindle cell neoplasms. |
format | Online Article Text |
id | pubmed-3391798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33917982012-07-11 Malignant solitary fibrous tumor in the extremity: Cytopathologic findings Khanchel, Fatma Driss, Maha Mrad, Karima Romdhane, Khaled Ben J Cytol Case Report Malignant solitary fibrous tumor (SFT) is an extremely rare neoplasm. There are only rare published accounts of the cytopathologic features of this tumor. We report a case of a 59-year-old woman presented with a 10-year history of a right thigh mass. A preoperative fine needle aspiration (FNA) was performed. Smears were hypercellular, with cohesive and crowded tissue fragments, haphazard cell arrangements and many single cells. The tumor cells were polymorphous, plump spindled or round with often indented or bare nuclei. A differential diagnosis of low grade sarcoma was favored. The diagnosis of malignant SFT is extremely difficult on FNA and must be included in the differential diagnosis of spindle cell neoplasms. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3391798/ /pubmed/22787298 http://dx.doi.org/10.4103/0970-9371.97160 Text en Copyright: © Journal of Cytology 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 Khanchel, Fatma Driss, Maha Mrad, Karima Romdhane, Khaled Ben Malignant solitary fibrous tumor in the extremity: Cytopathologic findings |
title | Malignant solitary fibrous tumor in the extremity: Cytopathologic findings |
title_full | Malignant solitary fibrous tumor in the extremity: Cytopathologic findings |
title_fullStr | Malignant solitary fibrous tumor in the extremity: Cytopathologic findings |
title_full_unstemmed | Malignant solitary fibrous tumor in the extremity: Cytopathologic findings |
title_short | Malignant solitary fibrous tumor in the extremity: Cytopathologic findings |
title_sort | malignant solitary fibrous tumor in the extremity: cytopathologic findings |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391798/ https://www.ncbi.nlm.nih.gov/pubmed/22787298 http://dx.doi.org/10.4103/0970-9371.97160 |
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