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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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Autores principales: Khanchel, Fatma, Driss, Maha, Mrad, Karima, Romdhane, Khaled Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
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.
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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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